๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2025-08-28

FAMily-centered WEight Loss for Black Adults (FAM WEL B-ing) (NCT06724406)

FAMily-centered WEight Loss for Black Adults (FAM WEL B-ing): Optimization and Evaluation Using Multiphase Optimization Strategy (MOST) and Social Network Analysis (SNA)

๐ŸŸข Recruiting Observational / Diagnostic ๐Ÿง  Behavioral & Psychological Program Sponsor: University of North Carolina, Chapel Hill

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The goal of this clinical trial is to learn the best combination of family components that yields optimal weight loss among Black adults. The main question it aims to answer is: What combination of four family components in combination with a standard behavioral weight loss program yields optimal weight loss among Black adults? Researchers will compare different combinations of family skills components (communication content, cohesion content, number of sessions, and mode of delivery) to see the best weight loss. Participants will: * Participate in a 6-month behavioral weight loss intervention * Attend core weight loss in-person group sessions, and dyad based family sessions * Keep track of weight, dietary intake and physical activity

Who can join: Review the eligibility criteria below.

Location: University of North Carolina at Chapel Hill โ€” Chapel Hill, North Carolina

Age range: 18 Years to 75 Years

๐Ÿงช Interventions in This Study

  • Family Skills Training Session Quantity: 5 (BEHAVIORAL)
  • Family Skills Training Session Mode: In-person (BEHAVIORAL)
  • Family Skills Training Content: Communication (BEHAVIORAL)
  • Family Skills Training Content: Cohesion (BEHAVIORAL)
  • Family Skills Training Session Quantity: 10 (BEHAVIORAL)
  • Family Skills Training Session Mode: Online (BEHAVIORAL)
  • Family Skills Training Content: No Communication (BEHAVIORAL)
  • Family Skills Training Content: No Cohesion (BEHAVIORAL)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (1 Sites)

  • University of North Carolina at Chapel Hill โ€” Chapel Hill, North Carolina

๐Ÿ“ž Contact the Study Coordinator

Phone: (919) 966-0360

Email: cdsamuel@email.unc.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—