Skip to main content
2026 Prospectus
Diabetes Alert Day 2026 approved hero showing a patient and interdisciplinary care team reviewing glucose trends and an early-action plan.

· Executive Brief

Diabetes Alert Day 2026

Turn risk awareness into appropriate testing, diagnosis, prevention support, and sustained care.

Greg Wahlstrom in his office at The Healthcare Executive
Written byMBAHCMPresident and Chief Executive Officer, The Healthcare ExecutiveOctober 2026 28 min read

The 2026 leadership signal

A wake-up call needs a reachable next step.

Diabetes risk tools can start a conversation but cannot distinguish type, establish a diagnosis, or replace laboratory testing and clinical assessment.

Executives should connect risk awareness with appropriate testing, clear result communication, diabetes prevention services for eligible people, and timely support for all forms of diabetes.

Audit one population from risk identification through completed testing, diagnostic disposition, and the first prevention or treatment connection.

U.S. burden

40 million+

The American Diabetes Association reported in 2026 that more than 40 million Americans were living with diabetes.

Unaware

1 in 4

The ADA reported that 1 in 4 U.S. adults with diabetes did not know they had it.

Prediabetes

115 million+

The ADA reported that more than 115 million people in the United States were living with prediabetes.

Figures are summarized from the authoritative sources linked below. Definitions and denominators should be read with each source.

Executive opening

A risk alert is only as strong as the step that follows it

Diabetes Alert Day asks people to learn their risk. For a health system, the harder question is what happens after someone learns it. Risk awareness creates value only when testing is reachable, results are explained and eligible people are connected to prevention. Recent studies show that each of those steps can fail on its own, and that some promising detection routes sit outside the clinic.[1][3]

Community pharmacies are a clear example. In a Scottish feasibility study across 16 pharmacies, point-of-care HbA1c testing found prediabetes in 15% of 499 high-risk adults.[1] Of the people with prediabetes, 51% enrolled in a digital prevention program.[1] In rural New South Wales, by contrast, only 15% of people referred from pharmacy screening attended follow-up testing with a general practitioner.[3] The same entry point produced very different follow-through depending on how the next step was built.

Eligibility rules matter as much as venues. Among U.S. young adults aged 18 to 34 with prediabetes, one in three (32.7%) would not have qualified for screening under current American Diabetes Association criteria.[4] A system that relies only on criteria-triggered testing will therefore miss a meaningful share of people who could benefit from early prevention.[4]

This brief adds the evidence behind the live page’s route, dashboard and plan. It examines the burden of undetected dysglycemia, the points where screening fails to become diagnosis or enrollment, and how access and equity shape those losses. It also looks at the people who carry each handoff and at how leaders can communicate risk in ways that earn a response. The executive question throughout is simple. Does a positive risk signal reliably reach a confirmed result and a program that a person actually starts?

Current evidence

What the research says about undetected prediabetes and its reach

Undetected dysglycemia is common wherever systems look for it. In 15 community pharmacies in the United Arab Emirates, trained pharmacists screened 1,320 adults with point-of-care HbA1c testing.[2] Of those screened, 24.3% had previously undetected prediabetes and 12.0% had HbA1c levels consistent with diabetes.[2] The service was designed for early detection among asymptomatic adults, not patients presenting with complaints.[2] For a health system, that is a reminder that the people most in need of a test may never book a visit to ask for one.

High-risk families carry a concentrated burden. In a cross-sectional study of 1,029 first-degree relatives of people with type 2 diabetes, 39.1% had prediabetes and 9.2% had undiagnosed diabetes under a single diagnostic criterion.[5] The test chosen changed the answer. Prediabetes prevalence was 18.4% by fasting plasma glucose, 18.0% by the two-hour glucose tolerance test and 30.9% by HbA1c.[5] The authors found that fasting glucose performed worst and judged HbA1c a feasible tool for large-scale screening in high-risk groups.[5]

Prediabetes is not a neutral waiting state. In a Greek outpatient cohort of 160 adults with prediabetes, 27 (16.9%) already had distal symmetrical polyneuropathy at baseline.[11] Among the remaining 133 participants, 13 developed it over 24 months, an incidence of 9.8%.[11] A meta-analysis of eight cross-sectional studies with 18,040 participants found higher odds of obstructive sleep apnea among people with prediabetes (odds ratio 2.78).[12] In a Peruvian occupational cohort, screening-detected prediabetes was associated with a higher hazard of incident caries (adjusted hazard ratio 1.94).[13]

For executives, these associations matter less as clinical detail than as operating signals. They show that early dysglycemia touches neurology, sleep, dental and occupational health services that rarely share a risk list.[11][12][13] A detection effort that ends at the glucose result leaves those connections unused. One that shares the finding across services creates more chances for coordinated, earlier attention.

Age also changes what a positive result means. A review of prediabetes in children and adolescents notes that insulin sensitivity improves after puberty, so glucose metabolism normalizes spontaneously in most young people.[10] For that reason, general population screening in youth is not recommended except in certain high-prevalence populations.[10] The review also highlights the limits of applying adult diagnostic criteria to children, so pediatric and adult pathways need separate rules and separate measures.[10] A single enterprise screening rule applied to every age group will produce misleading findings in both directions.

Figure 1

Detection works, but the next step decides whether it counts

Detection works, but the next step decides whether it countsPercent of the stated study group at each pathway step, as reported in each study. Values are copied from the cited studies [1], [2], [3], [4]; none is estimated.0%25%50%75%100%Previously undetected prediabetes foundat pharmacy screeningPreviously undetected prediabetes found at pharmacy screening: 24.3% (source [2])24.3%[2]Prediabetes found by pharmacy point-of-care HbA1cPrediabetes found by pharmacy point-of-care HbA1c: 15% (source [1])15%[1]Pharmacy-identified prediabetes enrolledin digital preventionPharmacy-identified prediabetes enrolled in digital prevention: 51% (source [1])51%[1]Attended follow-up testing afterpharmacy referralAttended follow-up testing after pharmacy referral: 15% (source [3])15%[3]Young adults with prediabetes noteligible for screeningYoung adults with prediabetes not eligible for screening: 32.7% (source [4])32.7%[4]Source [2]Source [1]Source [3]Source [4]Shade and hatching group bars by study; the studies differ in population and setting, so bars compare only within a shade

Percent of the stated study group at each pathway step, as reported in each study. Values are copied from the cited studies [1], [2], [3], [4]; none is estimated.

Data note. These values come from different studies, countries, populations and denominators, so this is an indirect comparison; the bars show where detection pathways gain or lose people, not how one program outperforms another.

Limitation. Each value reflects its own setting and definition; the rural follow-up figure has no stated denominator in the abstract, and the screening-eligibility figure is a modeled application of criteria to survey data.

Figure data (5 rows)
Figure 1 data: Detection works, but the next step decides whether it counts
MeasureValuePopulation, setting and year as reportedSource
Previously undetected prediabetes found at pharmacy screening24.3%321 of 1,320 adults screened in 15 community pharmacies, United Arab Emirates[2]
Prediabetes found by pharmacy point-of-care HbA1c15%75 of 499 high-risk adults, 16 community pharmacies, NHS Tayside, Scotland, February 2024 to January 2025[1]
Pharmacy-identified prediabetes enrolled in digital prevention51%38 of 75 participants with prediabetes, NHS Tayside, Scotland[1]
Attended follow-up testing after pharmacy referral15%People referred to general practitioners after abnormal results, rural Western New South Wales pharmacy pilot, January to May 2023[3]
Young adults with prediabetes not eligible for screening32.7%U.S. adults aged 18 to 34 with prediabetes, national survey data 2007 to 2016, under current American Diabetes Association criteria[4]
A pharmacist walks a middle-aged South Asian man through a short paper diabetes risk questionnaire.
Illustrative image. Pharmacy point-of-care testing found previously undetected prediabetes in 24.3% of adults screened in one program.[2]

Continuum of care

Where screening fails to become diagnosis and enrollment

The weakest link is usually the step after the first abnormal result. In the rural New South Wales pilot, everyone with an abnormal HbA1c or random glucose result was referred to a general practitioner and followed up by a clinician.[3] Even so, only 15% attended follow-up testing, and 44% of those who attended were diagnosed with diabetes.[3] The authors concluded that effective linkage to primary care remains a significant challenge.[3] In operating terms, the referral was sent, but the loop was never closed. The pilot shows why a referral count is not a useful measure of success on its own.

Pathways that remove a handoff look different. In the Scottish study, pharmacies referred people with HbA1c of 42 to 47 mmol/mol directly to a digital prevention program rather than back to a general practice.[1] Of 75 people with prediabetes, 38 (51%) enrolled.[1] Of 19 people with HbA1c at or above 48 mmol/mol, 17 attended their general practitioner.[1] Direct referral shortened the chain that a person had to complete alone. It also gave the pharmacy a clear destination for each result category, which reduced the judgment calls left to the person being screened.

The UAE program built the handoff into its design. Pharmacists systematically referred participants with identified prediabetes to an online prevention program, where diabetes educators delivered culturally appropriate, personalized sessions.[2] The screening stage lasted two to four months per pharmacy, while the prevention program averaged six months.[2] Detection and prevention run on different clocks, so ownership must extend well past the screening event.

Measurement can break the continuum as well. In the Peruvian occupational cohort, only 12,049 of 79,660 workers (15.1%) had longitudinal dental follow-up.[13] The authors noted that limited follow-up reduces generalizability and may reflect uneven surveillance.[13] When follow-up data are this sparse, a system cannot tell whether people were lost or simply never measured. Closed-loop reporting should count everyone who should have been followed, not only those who were.

Enrollment is also not the finish line. In a feasibility program for kidney transplant candidates with obesity, participants attended 15 weekly virtual group sessions using the National Diabetes Prevention Program curriculum.[7] Participants attending at least half of the sessions had greater median weight loss than those with lower attendance, independent of GLP-1 use.[7] The authors concluded that session engagement, rather than medication alone, appeared to drive outcomes.[7]

Figure 3

Why the pathway breaks

Cause-and-effect diagram: People identified as at risk for diabetes do not reach a confirmed result and an attended prevention programUnranked qualitative cause-and-effect diagram for the outcome in the box: People identified as at risk for diabetes do not reach a confirmed result and an attended prevention program Causes are assembled from the cited literature [1], [2], [3], [4], [6], [7], [8], [9], [10], [13]; categories are not weighted and their order carries no meaning.People identified as at riskfor diabetes do not reach aconfirmed result and anattended prevention programPeopleProcessTechnologyEnvironmentPolicyMeasurement

People

  • Pharmacists screen without a named receiving clinician
  • Coaches and educators lack protected time for follow-up
  • Clinical staff not involved in recruitment and content design

Process

  • Abnormal results routed back to primary care with no tracking
  • No direct referral from screening to a prevention program
  • Screening and prevention run on different timelines with no shared owner

Technology

  • Partner-site results do not reach the accountable clinician’s record
  • Risk models lack subgroup validation
  • Digital programs raise unresolved privacy questions

Environment

  • Rural distance between pharmacy and general practice
  • Partner pharmacies drop out of pilots
  • Deprived neighborhoods underrepresented in clinic-based screening

Policy

  • Screening criteria miss many young adults with prediabetes
  • Navigation billing rules create administrative friction
  • Adult criteria applied to children and adolescents

Measurement

  • Follow-up counted only for people who returned
  • Enrollment tracked but session attendance not reported
  • Results not stratified by age and deprivation

Unranked qualitative cause-and-effect diagram for the outcome in the box: People identified as at risk for diabetes do not reach a confirmed result and an attended prevention program Causes are assembled from the cited literature [1], [2], [3], [4], [6], [7], [8], [9], [10], [13]; categories are not weighted and their order carries no meaning.

Data note. Qualitative; no frequencies are implied.

Limitation. Causes drawn from published studies may not all apply locally; validate them with frontline teams.

Figure data (6 rows)
Figure 3 data: Why the pathway breaks
CategoryCauses drawn from the cited literature
PeoplePharmacists screen without a named receiving clinician; Coaches and educators lack protected time for follow-up; Clinical staff not involved in recruitment and content design
ProcessAbnormal results routed back to primary care with no tracking; No direct referral from screening to a prevention program; Screening and prevention run on different timelines with no shared owner
TechnologyPartner-site results do not reach the accountable clinician’s record; Risk models lack subgroup validation; Digital programs raise unresolved privacy questions
EnvironmentRural distance between pharmacy and general practice; Partner pharmacies drop out of pilots; Deprived neighborhoods underrepresented in clinic-based screening
PolicyScreening criteria miss many young adults with prediabetes; Navigation billing rules create administrative friction; Adult criteria applied to children and adolescents
MeasurementFollow-up counted only for people who returned; Enrollment tracked but session attendance not reported; Results not stratified by age and deprivation

Access

Bringing risk testing to places people already use

Pharmacies extend the front door. In the UAE study, a survey of 279 community members found 84% acceptance of pharmacy-based screening, and 59% considered pharmacies suitable locations.[2] The authors described pharmacy screening as an entry point to prevention and a replicable framework for cardiometabolic services.[2] For a health system, that framing turns a retail partner into part of the referral network. It also raises practical questions about data sharing, result ownership and how partner staff reach a clinician when a value is high.

Feasibility is real but uneven. Of 17 pharmacies enrolled in the rural New South Wales pilot, 9 completed the study, recruiting 116 adults over five months.[3] The authors judged pharmacy-led screening operationally feasible in rural Australia and found substantial undiagnosed diabetes.[3] Losing nearly half of the participating sites is an operating risk in its own right. Contracts, training and practical support for partner pharmacies deserve the same attention as the testing itself.

Test selection is an access decision as well as a clinical one. Because fasting glucose performed worst among three criteria in high-risk relatives, the study authors favored HbA1c for large-scale screening.[5] Point-of-care HbA1c was a screening test in all three pharmacy studies reviewed here.[1][2][3] Leaders should confirm that results from partner sites flow into the record that the accountable clinician actually reviews. A point-of-care result that lives only on a paper slip or a partner system is easy to lose at the very moment it matters.

Other clinical settings offer additional doors. A Nigerian before-and-after study of 77 periodontitis patients, 45 with diabetes and 32 with prediabetes, suggested that a mouthrinse point-of-care test could support diabetes risk screening in dental and medical care.[14] A cross-sectional study of 97 patients with prediabetes and 44 controls linked static balance measures with prediabetes, although the model still needs external validation.[15] These tools are early, but they show that risk detection can sit inside services people already visit. Each new door, however, needs the same receiving clinician and result route as the pharmacy model.

Digital prevention can extend reach after detection. A narrative review found that automated and semi-automated digital programs show potential to support lifestyle change, improve engagement and reduce reliance on labor-intensive counseling.[9] It also cautioned that limited external validation, privacy concerns and uncertain long-term effectiveness still constrain routine use.[9]

System route

Connect awareness to confirmed action.

The route should distinguish risk assessment, screening, diagnosis, diabetes type, and individualized care.

The route at a glance

  1. Recognize risk
  2. Test appropriately
  3. Connect prevention
  4. Start and sustain care
  1. Recognize risk

    Use validated tools and current clinical criteria without blaming people for weight, behavior, or family history.

  2. Test appropriately

    Order and complete indicated laboratory testing, then confirm and classify results under current standards.

  3. Connect prevention

    Offer eligible people access to evidence-based diabetes prevention and address practical barriers.

  4. Start and sustain care

    Coordinate education, medicines, technology, nutrition, eye, kidney, foot, cardiovascular, and psychosocial care.

Reliability rule: Do not imply that type 1 diabetes is preventable through lifestyle change or that every person with prediabetes will develop type 2 diabetes.

Figure 2

The system route as one flow

The system route as one flowThe five stages of the system route described in this brief, drawn as one flow with a learning loop back to the start. The stages are the page’s original executive guidance, not a clinical protocol.Recognize riskTestappropriatelyConnectpreventionStart andsustain careLearning returns to the start of the route

The five stages of the system route described in this brief, drawn as one flow with a learning loop back to the start. The stages are the page’s original executive guidance, not a clinical protocol.

Data note. Shows sequence and handoffs only; it carries no counts or rates.

Limitation. Local processes may add, merge or reorder stages under organizational policy.

Figure data (4 rows)
Figure 2 data: The system route as one flow
StageWhat the stage requires
Recognize riskUse validated tools and current clinical criteria without blaming people for weight, behavior, or family history.
Test appropriatelyOrder and complete indicated laboratory testing, then confirm and classify results under current standards.
Connect preventionOffer eligible people access to evidence-based diabetes prevention and address practical barriers.
Start and sustain careCoordinate education, medicines, technology, nutrition, eye, kidney, foot, cardiovascular, and psychosocial care.

Equity and trust

Who current detection pathways leave out

Criteria-based screening leaves predictable gaps. The finding that 32.7% of U.S. young adults with prediabetes would not qualify for screening points to a younger group that standard eligibility rules underserve.[4] Systems that test only when criteria trigger an alert should examine who falls outside those criteria in their own population. Age, insurance, language and neighborhood are reasonable starting points for that review. The aim is not to test everyone, but to know which groups the current rules consistently pass over.

Venue changes who is reached. In the Scottish study, pharmacies recruited relatively younger participants from more deprived backgrounds than the general practice comparison group.[1] Among pharmacy participants, 63% lived in the two most deprived area categories, compared with 33% in the general practice cohort.[1] The authors concluded that pharmacies provided effective, equitable access to testing and prevention for people being missed by current pathways.[1] For systems serving deprived neighborhoods, a partner venue may reach people that clinic invitations do not. That reach only becomes equity when results and referrals return to an accountable team.

Cultural fit is part of access. Before launch, the UAE team ran stakeholder surveys and interviews, held focus groups, translated and culturally adapted the Diabetes Prevention Program and trained participating pharmacists.[2] That preparation phase is easy to compress under deadline pressure. Yet it was the step designed to make the prevention offer usable by the community it served.[2] Health systems adopting a prevention curriculum should budget time for adaptation and partner training, rather than treating translation as a final formatting task.

New tools carry their own equity risks. The review of artificial intelligence in prediabetes care flagged limited external validation across diverse populations and a geographic imbalance in the evidence.[9] It called for multi-center, prospective and implementation-focused studies to establish equity, safety and cost-effectiveness before wider adoption.[9] Leaders evaluating vendor risk models should ask for subgroup performance in populations like their own. A model that performs well on average can still miss the groups an equity plan is meant to protect.

Age-specific rules are an equity issue too. The pediatric review warns that adult-based diagnostic criteria do not transfer cleanly to youth.[10] Stratified dashboards should therefore separate children, young adults and older adults, so that a strong overall rate does not hide a group the pathway was never designed to reach.

A nurse practitioner explains test results to the man from the pharmacy and his wife in an exam room.
Illustrative image. In one Scottish program, pharmacies reached participants from more deprived backgrounds than general practice screening did.[1]

Human infrastructure

The people who carry the risk-to-prevention handoff

Pharmacists, educators and coaches did the core work in these studies. In the UAE program, trained pharmacists delivered evidence-based screening protocols, and diabetes educators delivered the prevention sessions.[2] In the kidney transplant program, trained lifestyle coaches led the group sessions, with interprofessional pharmacotherapy management and remote monitoring alongside.[7] In that program, GLP-1 therapy use rose from 62.1% at baseline to 72.4% at session 15, and 52.4% reached high-dose therapy.[7]

Clinician involvement shapes adoption. In an evaluation of TeenLyft, a six-month behavioral program adapted from the Diabetes Prevention Program for adolescents having bariatric surgery, adoption was influenced by clinical staff involvement.[8] Staff helped with recruitment, content development and aligning content with adolescent needs.[8] Of 76 adolescents who enrolled, 29 completed surgery, and participants said the program supported their physical and emotional health.[8] They also wanted more mental health content, which points to the staffing mix a program may need.[8] Programs adapted from the same prevention curriculum may need different team compositions for different populations.

Navigation needs administrative scaffolding. A commentary on Medicare principal illness navigation argues that coverage has not translated reliably into access because the main barriers are administrative and operational.[6] The billing practitioner must perform an initiating visit and remains responsible for supervision, documentation and billing, even when navigators work outside the practice.[6] The authors cite the Medicare Diabetes Prevention Program as an example where CMS modified delivery rules once operational barriers emerged.[6]

Technology can support the workforce, but it does not replace it. The artificial intelligence review describes these tools as assistive technology that may support earlier detection, more precise risk stratification and scalable lifestyle management.[9] It also identifies the need for stronger governance frameworks.[9] In practice, that means someone must own model monitoring, staff must know when to override a score and patients must know a person is accountable for their result.

For executives, the lesson is that every role in the chain needs a defined scope, a referral destination and a way to see whether the person arrived. Pharmacist screening without a receiving clinician, or coaching without protected time, recreates the same leak in a new place. Workforce plans should therefore be built around the handoff, with each role’s caseload sized to the referral volume the screening effort will generate.

Operating dashboard

Measure testing, diagnosis, connection, and equity.

Separate type 1, type 2, gestational diabetes, and prediabetes where clinically and analytically appropriate.

Four operating signals

Testing completionDiagnostic closureProgram connectionAccess equity

Each signal pairs an executive question with one candidate local measure, set out below.

01

Testing completion

Track risk-based testing from order to completed result.

Measure
Eligible people completing laboratory testing

02

Diagnostic closure

Follow abnormal results to confirmation, classification, and documented communication.

Measure
Abnormal results with completed disposition

03

Program connection

Measure completed entry into selected prevention or diabetes-care services.

Measure
People completing first program or care visit

04

Access equity

Review completion and delay across priority populations.

Measure
Gap in completion and time by group

Figure 4

The operating system behind the dashboard

The operating system behind the dashboardThe four operating signals from this brief’s dashboard, each tied to the candidate owner named in the executive scorecard, around one accountable route. Drawn from the page’s original executive guidance.Accountableoperating route(executive sponsor)Testing completionOwner: Primary care and populationhealthDiagnostic closureOwner: Clinical qualityProgram connectionOwner: Care managementAccess equityOwner: Access and equity leaders

The four operating signals from this brief’s dashboard, each tied to the candidate owner named in the executive scorecard, around one accountable route. Drawn from the page’s original executive guidance.

Data note. Structural diagram; no measured values.

Limitation. Owners are candidates to be confirmed locally.

Figure data (4 rows)
Figure 4 data: The operating system behind the dashboard
Operating signalCandidate owner
Testing completionPrimary care and population health
Diagnostic closureClinical quality
Program connectionCare management
Access equityAccess and equity leaders

Handoff workflow

Carry the result, urgency, and next responsibility forward.

People should not receive an abnormal value without a clear explanation and a reachable care plan.

How responsibility moves

Lane 1Risk tool to clinician3 steps
Lane 2Laboratory to diagnosis3 steps
Lane 3Diagnosis to longitudinal support3 steps

Lane

Risk tool to clinician

  1. Explain that the result is not a diagnosis.
  2. Arrange appropriate testing.
  3. Give urgent symptom guidance.

Lane

Laboratory to diagnosis

  1. Notify the accountable clinician.
  2. Communicate the result and uncertainty.
  3. Confirm the follow-up appointment.

Lane

Diagnosis to longitudinal support

  1. Clarify type and treatment plan.
  2. Connect education, supplies, and coverage help.
  3. Assign monitoring and escalation responsibilities.

A referral to a prevention program is not appropriate for every diabetes type or every abnormal result. Use confirmed eligibility and patient choice.

Executive scorecard

Ask whether awareness reaches diagnosis and support.

Avoid celebrating risk-test volume when testing and care remain inaccessible.

Who reviews what

  • Primary care and population health
  • Clinical quality
  • Care management
  • Access and equity leaders

Candidate owners named in the scorecard, confirmed locally.

Use stable definitions and stratify results by site, population, and service line when appropriate.
SignalExecutive questionAccountable ownerReview cadence
RecognitionAre high-risk people offered an appropriate next step?Primary care and population healthMonthly
ClosureHow many abnormal results remain unresolved?Clinical qualityWeekly
ConnectionDo eligible people complete prevention or diabetes-care entry?Care managementMonthly
EquityWhich groups face the longest delay or highest abandonment?Access and equity leadersQuarterly

Figure 5

Control points for a closed-loop diabetes risk pathway

Figure 5: Control points for a closed-loop diabetes risk pathway
Control pointRisk if missingOwnerEvidence of control
Agreed screening test and eligibility rules, including people outside standard criteriaHigh-risk young adults and relatives are never testedPrimary care medical director with population health leadShare of the at-risk population with a documented HbA1c in the review period
Named receiving clinician for every partner-site abnormal resultAbnormal results go unconfirmed after pharmacy referralAmbulatory quality lead and pharmacy partnership managerShare of abnormal partner results with confirmatory testing completed
Direct referral route from confirmed prediabetes to a prevention programPeople must complete several handoffs alone and drop outPopulation health director and prevention program managerShare of confirmed prediabetes referred and enrolled
Attendance tracking after enrollmentEnrollment counts hide low engagementPrevention program managerShare of enrollees attending at least half of sessions
Partner site support and retentionPharmacies leave the program and access shrinksCommunity partnership leadActive partner sites at each quarterly review
Stratified reporting by age, deprivation and languageOverall rates hide groups the pathway does not reachHealth equity officerCompletion gaps by group reviewed quarterly
Validation and privacy review for digital and risk-model toolsTools underperform or erode trust in some populationsChief medical information officerDocumented subgroup performance and privacy assessment before go-live

Control points derived from the cited evidence [1], [2], [3], [4], [5], [7], [9] and this brief’s executive guidance.

Data note. Each row is a control to verify, not a measured result.

Limitation. Owners and evidence of control must follow local policy and applicable requirements.

Public communication

Communicating risk so that people take the next step

Trust problems are often administrative before they are clinical. The navigation commentary describes a broader trust problem in the administrative pathway that makes clinicians cautious, even when a service is covered.[6] It recommends plain-language guidance, clearer risk boundaries and simpler enrollment and payment pathways.[6] It also calls for measuring activation, onboarding time and successful service delivery.[6] Referral partners in diabetes prevention need the same clarity before they will promote a program with confidence.

Channels should match the audience. TeenLyft delivered online educational videos and added social media platforms during implementation to boost engagement.[8] Adolescents emphasized that the program gave them education and skills to support weight management after surgery.[8] In the UAE program, educators delivered personalized sessions designed to be culturally appropriate for participants.[2] Neither program relied on a single generic leaflet. Both shaped the format and the channel around the people they needed to reach.

Messages should not depend on an invitation that some people will never receive. Because one in three young adults with prediabetes would fall outside current screening criteria, public campaigns that tell people to wait for a clinician’s prompt may miss them.[4] Messages for families of children need a different tone. The pediatric review notes that lifestyle modification remains the primary intervention because drug treatments have yet to show efficacy in youth.[10]

Specialty services can repeat the same message. The sleep apnea meta-analysis authors supported considering sleep apnea screening in people with prediabetes, which gives sleep and primary care teams a shared conversation.[12] Dental teams have a similar opening. Screening-detected prediabetes was associated with incident caries in working adults, and a mouthrinse point-of-care test has been proposed to support risk screening in dental care.[13][14] Consistent language across these services makes a single risk finding easier to act on. When a dentist, a sleep clinician and a primary care team describe the same result in the same way, people receive one clear message instead of three partial ones.

Finally, communication should be judged by response, not reach. A result message counts as complete when the person understands what it means, knows the next step and has a way to take it. That standard turns Diabetes Alert Day from a campaign into a measurable service. It also gives communication teams a shared outcome with clinical teams, instead of a separate count of impressions or materials distributed.

The man and his wife walk together on a park path lined with spring blossoms.
Illustrative image. In one program using a diabetes prevention curriculum, participants who attended more sessions lost more weight.[7]

90-day plan

Close one diabetes detection gap in 90 days.

Choose a population with low testing completion or high unresolved abnormal results.

Ninety days, three moves

  1. Days 1–30Trace the alert
  2. Days 31–60Test closed-loop action
  3. Days 61–90Make early action routine

Days 1–30

Trace the alert

  • Map risk through diagnosis and connection.
  • Review 30 recent cases.
  • Baseline completion and disparities.

Days 31–60

Test closed-loop action

  • Pair risk assessment with lab access.
  • Create an abnormal-result worklist.
  • Warm-transfer eligible services.

Days 61–90

Make early action routine

  • Compare completion and delay.
  • Embed ownership and escalation.
  • Set the next prevention or care target.

Figure 6

The 90-day plan on one timeline

The 90-day plan on one timelineThe 90-day plan from this brief drawn as a timeline: each action sits in the 30-day window the plan assigns it. The full wording of each action is in the figure data and in the plan above.Day 0Day 30Day 60Day 90Map risk through diagnosis and connection.Days 1–30: Map risk through diagnosis and connection.Review 30 recent cases.Days 1–30: Review 30 recent cases.Baseline completion and disparities.Days 1–30: Baseline completion and disparities.Pair risk assessment with lab access.Days 31–60: Pair risk assessment with lab access.Create an abnormal-result worklist.Days 31–60: Create an abnormal-result worklist.Warm-transfer eligible services.Days 31–60: Warm-transfer eligible services.Compare completion and delay.Days 61–90: Compare completion and delay.Embed ownership and escalation.Days 61–90: Embed ownership and escalation.Set the next prevention or care target.Days 61–90: Set the next prevention or care target.Days 1–30Days 31–60Days 61–90

The 90-day plan from this brief drawn as a timeline: each action sits in the 30-day window the plan assigns it. The full wording of each action is in the figure data and in the plan above.

Data note. Time boxes are a management framework, not a clinical timeline.

Limitation. Durations are uniform 30-day windows; real tasks may span windows.

Figure data (9 rows)
Figure 6 data: The 90-day plan on one timeline
WindowAction
Days 1–30Map risk through diagnosis and connection.
Days 1–30Review 30 recent cases.
Days 1–30Baseline completion and disparities.
Days 31–60Pair risk assessment with lab access.
Days 31–60Create an abnormal-result worklist.
Days 31–60Warm-transfer eligible services.
Days 61–90Compare completion and delay.
Days 61–90Embed ownership and escalation.
Days 61–90Set the next prevention or care target.

An alert matters only when action is possible.

Diabetes Alert Day 2026 should help people move from risk awareness to accurate diagnosis and appropriate support without stigma.

Executive action

Sponsor one closed-loop risk-to-diagnosis pilot and review testing, diagnostic closure, and service connection within 90 days.

Operational readiness verification

Make the observance visible in everyday operations.

Diabetes Alert Day becomes meaningful when people move from risk identification to appropriate testing, result communication, prevention or treatment, and follow-up. The weak version is a message without an operating change. The stronger version defines what teams should see, who owns each transition, how exceptions escalate, and how leaders know that the pathway actually closed.

The principal failure mode is that risk screening can become a one-day event without diagnostic confirmation, understandable results, prevention support, or ongoing care. Leaders should test the route with recent cases, frontline staff, patients or community partners, and the teams that receive the next handoff. That review should distinguish a written policy from reliable execution under real workload, staffing, access, and communication conditions.

Recognize risk

Confirm the accountable owner, expected evidence, exception route, communication standard, and documented closure for this step.

Test appropriately

Confirm the accountable owner, expected evidence, exception route, communication standard, and documented closure for this step.

Connect prevention

Confirm the accountable owner, expected evidence, exception route, communication standard, and documented closure for this step.

Start and sustain care

Confirm the accountable owner, expected evidence, exception route, communication standard, and documented closure for this step.

Testing completion

Confirm the accountable owner, expected evidence, exception route, communication standard, and documented closure for this step.

An equity review should review food access, coverage, language, geography, transportation, digital access, and pharmacy affordability. Aggregate performance can hide a pathway that works for people with the fewest barriers while failing those who need language support, accommodations, transportation, trusted outreach, flexible scheduling, or help navigating coverage. Stratified results and direct feedback should therefore guide the improvement plan.

Measurement should pair screen-positive follow-up, diagnostic completion, result communication, prevention enrollment, and continuity. Counts alone do not establish reliability. The executive review should examine time, completion, unresolved exceptions, patient or workforce experience, and variation across sites. A small set of stable measures is more useful than a large dashboard that no one owns.

Governance should align primary care, laboratory, pharmacy, nutrition, population health, and community programs under one risk-to-action pathway. The accountable owner should convene the relevant clinical, operational, access, quality, and community voices; remove barriers that frontline teams cannot solve; and return decisions to the people doing the work. The 90-day test is simple: show which failure point changed, what evidence confirms the change, and what still requires executive action.

Executive action kit · Day observance

Turn Diabetes Alert Day into accountable action.

Turn risk awareness into appropriate testing, diagnosis, prevention support, and sustained care.

Take it with you

Filed under

Chronic Disease and Specialty CarePublic Health and PreventionDay

Leadership focus

Use this observance to examine navigation, longitudinal ownership, and specialty-care coordination. Select one verified barrier, assign an accountable owner, and carry the improvement beyond the campaign window.

Workforce lens

Ask whether staffing, role clarity, training, tools, workload, and escalation support the people operating the information, access, longitudinal ownership, and follow-through pathway.

Patient and community lens

Make the approved first step clear. Test whether a person can move from information to an acknowledged next action without navigating conflicting instructions.

Equity and access lens

Review language, transportation, affordability, food access, digital access, disability, and geographic availability.

Five-minute briefing

Inspect the operating sequence

Listen with people using the pathway, caregivers, primary care, specialty services, pharmacy, and community partners. Find one a confusing entry point, fragmented follow-through, or an unresolved navigation need, then test the locally approved route from entry through acknowledged follow-through.

  1. Recognize risk
  2. Test appropriately
  3. Connect prevention
  4. Start and sustain care
Leadership actions for this week
  • Name an executive sponsor and frontline operating owner.
  • Ask people using and operating the pathway where ownership becomes unclear.
  • Test one representative route from first question to acknowledged next step.
  • Select one barrier that can be corrected without overstating the evidence.
  • Set a review date and define how completion will be verified.
Candidate measures

Define every numerator, denominator where relevant, owner, data source, exclusions, cadence, and limitation locally. These are management prompts, not external benchmarks.

  • Eligible people completing laboratory testing
  • Abnormal results with completed disposition
  • People completing first program or care visit
Department readiness checklist
  • The public and staff entry points match the actual approved process.
  • A specific role accepts each request, referral, or escalation.
  • Handoffs include acknowledgment and a visible unresolved state.
  • Language, disability, digital, transportation, and trust barriers receive explicit review.
  • Communications do not introduce unsupported themes, statistics, or clinical advice.
  • A named leader will review what changed after the observance.
Intended audiences
  • Executive and Operational Leaders
  • Patient Experience and Access Leaders
Staff communication template

During Diabetes Alert Day, our organization will connect awareness with a practical review of the information, access, longitudinal ownership, and follow-through pathway. Use approved information, identify the correct entry point, confirm ownership when work moves, protect privacy, and escalate unresolved barriers through local channels.

Community communication template

Diabetes Alert Day is an opportunity to share trustworthy information and make the next step easier to find. Use our approved channels for information and support. If a request changes hands, our goal is to keep ownership and follow-through visible.

Measurement worksheet
Signal
What observable condition will show whether the route works?
Definition
What is included, excluded, and counted?
Owner
Who reviews the signal and acts on exceptions?
Cadence
When will leaders review it?
Equity check
Which differences require protected, locally appropriate review?
Closure
What evidence will confirm the improvement was completed?
Editorial review
Completed
Source records
2 listed under Authoritative resources
Review standard
Sourced facts remain separated from original executive guidance
Clinical boundary
No new statistical or clinical claim was added by this action kit

Authoritative resources

Source note: Healthgrades uses “American Diabetes Alert Day.” The American Diabetes Association’s official 2026 pages use the trademarked name “Diabetes Alert Day.” Use the organizer’s official name.

Safety note: A risk test does not diagnose diabetes. Vomiting, abdominal pain, deep or difficult breathing, confusion, severe weakness, loss of consciousness, or a severe low or high glucose emergency requires immediate medical help under the person’s emergency plan or emergency services.

ADA confirms Tuesday, March 24, 2026 and uses “Diabetes Alert Day,” not the Healthgrades name. “Learn Your Risk” is the title of the ADA’s 2026 press release and campaign call, but it is not labeled as a formal official theme, so `official_theme` remains null.

Peer-reviewed references

References

Fifteen peer-reviewed sources, newest first. Each was individually verified through authenticated academic research databases. Bracketed numbers in the text link here; the original executive guidance on this page carries no citations because it is guidance, not a sourced claim. Sources last checked in those databases on .

  1. 1. Detection of prediabetes and undiagnosed type 2 diabetes in underserved communities using community pharmacy point-of-care testing: A prospective feasibility study. Diabetic Medicine. 2026;43(7):e70368. https://doi.org/10.1111/dme.70368
  2. 2. Designing and implementing a prediabetes screening in community pharmacies and online prevention program: findings from the PREDICT study. BMC Public Health. 2026;26(1):1880. https://doi.org/10.1186/s12889-026-27437-7
  3. 3. Expanding Access to Early Diabetes Detection: A Pharmacy-Based Screening Pilot in Rural New South Wales. Health Science Reports. 2026;9(5):e72460. https://doi.org/10.1002/hsr2.72460
  4. 4. Screening gaps for prediabetes in US young adults under current American diabetes Association criteria. Diabetes Research and Clinical Practice. 2026;237:113339. https://doi.org/10.1016/j.diabres.2026.113339
  5. 5. Comparative analysis of three standard diagnostic criteria to detect prediabetes and diabetes in first degree relatives of people with T2DM. Journal of Diabetes & Metabolic Disorders. 2026;25(2):225. https://doi.org/10.1007/s40200-026-02045-9
  6. 6. A covered benefit with an untrusted on-ramp: Why medicare principal illness navigation still is not reaching patients. Journal of Cancer Policy. 2026;49:100794. https://doi.org/10.1016/j.jcpo.2026.100794
  7. 7. Feasibility of the Comprehensive Overweight/Obesity Management Pre-Kidney Transplant Program: A Group-Based Lifestyle Intervention and GLP-1 Receptor Agonist Therapy for End-Stage Kidney Disease Candidates Ineligible Due to Obesity. The Science of Diabetes Self-Management and Care. 2026:26350106261483738. https://doi.org/10.1177/26350106261483738
  8. 8. Evaluation of a behavioral intervention to support adolescents undergoing bariatric surgery using the reach, effectiveness, adoption, implementation, maintenance (RE-AIM) framework. Scientific Reports. 2026;16(1):22468. https://doi.org/10.1038/s41598-026-50810-w
  9. 9. Artificial intelligence in prediabetes care: applications in screening, risk prediction, and lifestyle intervention. Frontiers in Endocrinology. 2026;17:1885905. https://doi.org/10.3389/fendo.2026.1885905
  10. 10. Prediabetes in children and adolescents: what do we need to know?. Annals of Pediatric Endocrinology & Metabolism. 2026;31(3):160-167. https://doi.org/10.6065/apem.2550222.111
  11. 11. Incidence and predictors of distal symmetrical polyneuropathy in prediabetes: A 24-month prospective cohort study. Diabetes Research and Clinical Practice. 2026;239:113494. https://doi.org/10.1016/j.diabres.2026.113494
  12. 12. The association between prediabetes and obstructive sleep apnea syndrome: a meta-analysis. Frontiers in Endocrinology. 2026;17:1798827. https://doi.org/10.3389/fendo.2026.1798827
  13. 13. Baseline Prediabetes, Hyperglycemia, and Incident Dental Outcomes Among Peruvian Formal-Sector Workers: A Retrospective Occupational Cohort Study. Dentistry Journal. 2026;14(9):536. https://doi.org/10.3390/dj14090536
  14. 14. Periodontal Therapy-Related Changes in Clinical Parameters, Active-Matrix Metalloproteinase-8 and C-Reactive Protein in Prediabetes and Diabetes. Oral Diseases. 2026:odi.70481. https://doi.org/10.1111/odi.70481
  15. 15. Association of static balance parameters with prediabetes: a cross-sectional study and nomogram development. Frontiers in Endocrinology. 2026;17:1921238. https://doi.org/10.3389/fendo.2026.1921238

Claim-to-source matrix

What each source supports

Every sourced claim in the new sections maps to the references that support it, the section where it is used, and the limitation a reader should keep in mind. Original executive guidance carries no sources because it is guidance, not a finding.

Claim-to-source matrix
Claim groupSourcesYearsUsed inLimitation
Undetected prediabetes and diabetes found by community pharmacy point-of-care HbA1c testing[1] [2] [3]2026Current evidenceFeasibility and implementation studies in Scotland, the United Arab Emirates and rural Australia; high-risk or self-selected participants; no randomized comparison.
Screening criteria and test choice change who is identified[4] [5]2026Current evidenceU.S. survey data from 2007 to 2016 and a single cross-sectional study of first-degree relatives; findings may not transfer to other populations.
Prediabetes is associated with neuropathy, sleep apnea and dental outcomes[11] [12] [13]2026Current evidenceObservational designs; associations do not establish causation; single-center cohort and cross-sectional studies.
Follow-up after pharmacy referral and direct referral to prevention programs[1] [2] [3]2026Continuum of careSmall pilots with limited follow-up periods; denominators for some reported percentages are not stated in the abstracts.
Engagement in prevention-curriculum programs and staff roles in adoption[7] [8]2026Human infrastructureSingle-center, single-arm feasibility and RE-AIM evaluations in specialized surgical and transplant populations.
Equity of pharmacy-based access and cultural adaptation[1] [2]2026Equity and trustDeprivation comparison drawn from one Scottish region; cultural adaptation described for one national context.
Pediatric screening limits and age-specific criteria[10]2026Equity and trustNarrative review; no new primary data.
Alternative detection tools in dental, functional and digital settings[9] [14] [15]2026AccessEarly-stage tools; narrative review, single-arm and cross-sectional studies; external validation still required.
Administrative trust and navigation infrastructure[6]2026Public communicationPolicy commentary focused on Medicare principal illness navigation; no outcome data.
Greg Wahlstrom in his office at The Healthcare Executive

About the author

Greg Wahlstrom

MBAHCM

President and Chief Executive Officer, The Healthcare Executive

©2014 – 2026 The Healthcare Executive. All rights reserved.

Back to the contents

Health Observance Calendar

See next month’s observances before it starts.

One email ahead of each month with the health observances coming up and the executive briefs that go with them.

Sent by The Healthcare Executive. Unsubscribe at any time. See our Privacy Policy.