Clinical trial Recruiting at 1 site Interventional Ages 12 and up

Family-based diabetes prevention for parents and kids

Official title: Community Engaged Alliance-Reimagined Environments and Systems Together for Outcomes Georgia Through Research and Evaluation for Sustainability (RESTORES) - Georgia CEAL RESTORES

Run by Morehouse School of Medicine · NCT07808723 · Data updated 2026-11-12

A family-focused program tests whether a 12-week lifestyle plan can help parents at risk for diabetes lose weight and improve healthy habits for themselves and their children aged 12–17.

More Prediabetes trials

Quick facts

Study typeInterventional
Ages12 Years and up
SexAll
Enrollment120 (estimated)
SponsorMorehouse School of Medicine
Academic / other
Locations1 site (Atlanta, Georgia)
StatusRecruiting
StartedAugust 29, 2026
Main results expectedMarch 2028
Study endsMarch 2028
Registry record updatedSeptember 18, 2026
Trial IDNCT07808723 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Families where a parent/guardian is African American or Hispanic, 18+ years old, lives with a child aged 12–17, and has prediabetes or risk factors for diabetes.

Probably not a fit

Participants without showing weight loss or who do not engage with the 12-week program may see limited personal benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study assigns a 12-week, in-person family-based lifestyle intervention to parents with prediabetes or diabetes risk factors and their children. Primary outcome is weight loss in parents, with additional measures of weight, blood pressure, waist size, and lifestyle behaviors collected at baseline, after the program, and at a 3-month follow-up. Data are gathered via REDCap surveys and clinical assessments, including weekly parental weight checks and standard physical measurements. Participants attend 12 weekly sessions at a single site in Atlanta, GA, supported by Morehouse School of Medicine and NHLBI collaboration. The study aims to see if the program can promote sustainable healthy behaviors and family engagement to reduce type 2 diabetes risk.

Why it matters

Potential benefit: If successful, families may gain a structured approach to weight loss and healthier routines that reduce the risk of developing type 2 diabetes.

How similar studies have gone: Prior family-based lifestyle programs have demonstrated feasibility and weight-related outcomes in similar populations, though exact results vary by setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Parent/guardian must identify as African American or Hispanic
* Parent/guardian must be 18+ years residing in the same household as the child (i.e., biological or have legal guardianship for child)
* Parent/guardian must have prediabetes (HbA1c level 5.7-6.4%) or be at risk of developing Type 2 diabetes using CDC's Pre-Diabetes Risk Test
* Participant is willing to commit to participation in a 12-week, in-person, intervention study
* No plans to move over the next 9-months
* Parent/guardian should be ambulatory and able to participate in physical activity
* Children must be between the ages of 12-17 years old
* Child should be ambulatory and able to participate in physical activity

Exclusion Criteria:

* Severe psychological disorders that may prevent/interfere with study -participation
* Physical impairments that may prevent participation in moderate intensity physical activity
* Previous diagnosis of diabetes
* History of congestive heart failure
* Renal failure
* Recent (\<12 months) cardiovascular events such as myocardial infarction (heart attack) or stroke
* Taking medications that may affect endpoint analyses
* Have co-morbid contraindications to physical activity or dietary changes
* Currently pregnant or planning to become pregnant in the next year
* Family lives outside of Georgia

Where it's running

  • Morehouse School of Medicine
    Atlanta, Georgia, United States
    Recruiting

Study contacts

  • Principal investigator: Rakale C Quarells, PhD — Morehouse School of Medicine
  • Study coordinator: Katrina M Brantley, DrPH
  • Email: kbrantley@msm.edu
  • Phone: 470-670-7840

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.