NCT06557317 In-Person Lifestyle Program for Black Adolescent Girls at Risk for Type 2 Diabetes
| NCT ID | NCT06557317 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Cornell University |
| Condition | Behavior, Adolescent |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2024-08 |
| Primary Completion | 2024-12-31 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 60 participants in total. It began in 2024-08 with a primary completion date of 2024-12-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The aim of this study is to look at changes in diabetes-related risk factors in Black adolescent girls who are at risk for type 2 diabetes and their primary female caregiver after both participating in a 12-week in-person lifestyle program.
Eligibility Criteria
Inclusion Criteria for adolescent participants: * 12-18 years of age * self-identify as Black or African American * have obesity (\>=95th percentile BMI) Exclusion Criteria for adolescent participants: * pregnant or within 3 months postpartum. * participated in a formal weight management program within 6 months prior to study. * currently taking medications or diagnosed with a condition known to influence metabolism, physical activity ability, or cognitive function. * have previously undergone bariatric surgery. * have type 2 diabetes. * unable to speak English or have developmental conditions that interfere with ability to communicate. Inclusion Criteria for caregiver participants: * 18 years or older. * proficiency in speaking English. * live in the same household as the adolescent who will also be enrolled. * prepares the majority (\>50%) of meals in the household. Exclusion Criteria for caregiver participants: * pregnant or within 3 months postpartum. * unable to speak English or have developmental conditions that interfere with ability to communicate.
Contact & Investigator
Tashara M Leak, PhD, RD
PRINCIPAL INVESTIGATOR
Cornell University
Frequently Asked Questions
Who can join the NCT06557317 clinical trial?
This trial is open to female participants only, aged 12 Years or older, up to 18 Years, studying Behavior, Adolescent. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06557317 currently recruiting?
Yes, NCT06557317 is actively recruiting participants. Contact the research team at tml226@cornell.edu for enrollment information.
Where is the NCT06557317 trial being conducted?
This trial is being conducted at Brooklyn, United States.
Who is sponsoring the NCT06557317 clinical trial?
NCT06557317 is sponsored by Cornell University. The principal investigator is Tashara M Leak, PhD, RD at Cornell University. The trial plans to enroll 60 participants.