- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05370781
Michigan Men's Diabetes Project 2 (MenD 2)
September 8, 2025 updated by: Jaclynn Hawkins, University of Michigan
The Michigan Men's Diabetes Project 2 (MenD 2) is an 18-month pilot randomized clinical trial.
We are looking to recruit 60 Black men with type 2 diabetes (need to have diagnosis for at least 6 months) that are over the age of 21.
Interested participants need to be under the care of a physician for their diabetes, have access to reliable transportation for study activities, and be willing to participate in 4 health assessments where they will get their A1C, blood pressure, height, and weight measured and they will complete a survey.
All participants will receive 10 hours of diabetes self-management education with a Certified Diabetes Care and Education Specialist.
Participants randomized to the intervention arm will also be offered 6 months of monthly diabetes self-management support (DSMS) sessions with trained Peer Leaders who are also Black men with type 2 diabetes.
After the 6 months of support, this group will transition into 6 months of ongoing support where they can continue DSMS and/or other diabetes related initiatives that are important to the group and chosen by the group.
Due to the COVID-19 pandemic, DSME and DSMS sessions will likely be held via Zoom, ongoing support sessions have potential to be in person.
The 4 health assessments will take place at baseline, 3-months, 9-months, and 15-months.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
48
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Michigan
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Ann Arbor, Michigan, United States, 48109
- University of Michigan
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
17 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Black/African American males, age 21 years or older with diagnosis of T2D for six months, transportation to attend program activities, under the care of a physician for diabetes, and willing to attend group delivered sessions.
Exclusion Criteria:
- We considered restricting eligibility to a higher-risk population of participants with A1c ≥ 8%. Preliminary data suggest that over 50% of the proposed study sample will have an A1c ≥ 8%. Focusing on all older Black men with T2D allows us to cast a wide net for secondary prevention and public health impact.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Peer led diabetes self-management support (PLDSMS)
Participants in the PLDSMS arm will receive 10 hours of diabetes self-management education (DSME) with a certified diabetes care and education specialist.
This group will then transition into monthly 90-minute diabetes self-management support (DSMS) with trained peer leaders for 6 months.
After the DSMS sessions, the group will transition into 6 months of ongoing support and will be encouraged to continue DSMS through initiatives that are important to them.
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While the effectiveness of peer-led interventions delivering diabetes-related education and support for short-term clinical, psychosocial, and behavioral improvements is well-established, older Black men in particular are less likely to participate and are at a higher risk of drop-out from these studies.
This intervention aims to determine if using older Black men as peer leaders to other older Black men will improve retention rates for this population.
Participants will attend 10 hours of virtual group diabetes self-management education classes led by a certified diabetes care and education specialist through the online HIPPA compliant Zoom platform.
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Active Comparator: Control Group
Participants in the control group will receive 10 hours of diabetes self-management education (DSME) with a certified diabetes care and education specialist.
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Participants will attend 10 hours of virtual group diabetes self-management education classes led by a certified diabetes care and education specialist through the online HIPPA compliant Zoom platform.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Hemoglobin A1c
Time Frame: baseline, 3-months, 9-months, 15-months
|
Anthropometric/clinical data
|
baseline, 3-months, 9-months, 15-months
|
|
Change in Regimen Adherence
Time Frame: baseline, 3-months, 9-months, 15-months
|
Survey data
|
baseline, 3-months, 9-months, 15-months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Depression
Time Frame: baseline, 3-months, 9-months, 15-months
|
survey data
|
baseline, 3-months, 9-months, 15-months
|
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Change in Body Mass Index
Time Frame: baseline, 3-months, 9-months, 15-months
|
Anthropometric data/clinical data
|
baseline, 3-months, 9-months, 15-months
|
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Change in Blood Pressure
Time Frame: baseline, 3-months, 9-months, 15-months
|
Anthropometric data/clinical data
|
baseline, 3-months, 9-months, 15-months
|
|
Change in Diabetes Social Support
Time Frame: baseline, 3-months, 9-months, 15-months
|
survey data
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baseline, 3-months, 9-months, 15-months
|
|
Change in Diabetes-Related Distress
Time Frame: baseline, 3-months, 9-months, 15-months
|
survey data
|
baseline, 3-months, 9-months, 15-months
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Change in Diabetes Quality of Life
Time Frame: baseline, 3-months, 9-months, 15-months
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survey data
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baseline, 3-months, 9-months, 15-months
|
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Change in Adherence to gender norms
Time Frame: baseline, 3-months, 9-months, 15-months
|
survey data
|
baseline, 3-months, 9-months, 15-months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jaclynn Hawkins, PhD, University of Michigan, School of Social Work
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2022
Primary Completion (Estimated)
December 30, 2025
Study Completion (Estimated)
June 30, 2026
Study Registration Dates
First Submitted
May 3, 2022
First Submitted That Met QC Criteria
May 6, 2022
First Posted (Actual)
May 12, 2022
Study Record Updates
Last Update Posted (Estimated)
September 10, 2025
Last Update Submitted That Met QC Criteria
September 8, 2025
Last Verified
September 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HUM00200469
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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