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Trial · NCT07888179

Scaling up the DSMES Learning Collaborative

NCT07888179, Not applicable, Not yet recruiting, Mary Lacy

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Scaling up the DSMES Learning Collaborative. Trials, record NCT07888179. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07888179

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Scaling up the DSMES Learning Collaborative
NCT number
NCT07888179
Status
Not yet recruiting
Phases
Not applicable
Enrollment
96 participants, estimated
Lead sponsor
Mary Lacy
Conditions
Type Two Diabetes Mellitus
Interventions
Multicomponent Implementation Strategy (MCIS) Bundle, Standard of Care
First posted
2026-10-22
Last updated
2026-10-22

Source ClinicalTrials.gov

Registered outcomes5

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPercentage of Eligible Patients Referred to DSMES9 Months After Initiation of InterventionPercentage of eligible patients with diabetes who receive a referral to diabetes self-management education and support (DSMES).
SecondaryChange in Mean HbA1c for Patients with HbA1c >9%Baseline and monthly during active intervention through 12 month follow-up
HbA1c control will be extracted from the electronic health record and assessed as change in mean HbA1c from baseline to the end of the intervention and at 1-month and 12-month follow-up, and change in the percentage of patients with HbA1c greater than 9%.
SecondaryPercentage of Providers Referring Patients to DSMESBaseline and monthly during active intervention through 12 month follow-upPercentage of providers referring patients to DSMES, calculated as the number of providers referring patients to DSMES divided by the total number of providers at the clinic.
SecondaryChange in DSMES Referral Rate During the 12-Month Sustainment PeriodMonthly during the 12-month sustainment periodMaintenance will be measured as the change in DSMES referral rate over the 12-month assessment period.
SecondaryPercentage of Patients Completing DSMESBaseline and monthly during active intervention through 12 month follow-up
DSMES attendance will be extracted and reported by participating clinics. Attendance will be considered complete when a patient has attended 2 or more hours of DSMES, in alignment with state reporting.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07888179

GET https://conductscience.org/api/trials/v1/NCT07888179/registered