Support interventions for weight loss in African American families
A Peer and Family-Based Approach to Obesity in African American Families
This study tests whether support programs for parents and families can help African American families lose weight better than a regular cancer prevention program over a year.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 1200 (estimated) |
| Ages | 10 Years to 65 Years |
| Sex | All |
| Sponsor | M.D. Anderson Cancer Center Academic / other |
| Locations | 1 site (Houston, Texas) |
| Trial ID | NCT04644224 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of parent and family-oriented support interventions aimed at facilitating weight loss among African American families. It compares the outcomes of these interventions against a cancer prevention control group over a 12-month period. The study utilizes the RE-AIM model to assess various factors affecting the implementation and effectiveness of the interventions. Participants include parents or caregivers and their children, who will engage in health coaching sessions, resource navigation, and support groups.
Who should consider this trial
Good fit: Ideal candidates are African American parents or caregivers aged 18-65 who are overweight and have a child aged 8-17 living in the same household.
Not a fit: Patients who are currently pregnant or have contraindications for exercise will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to effective weight loss strategies for African American families, improving their overall health and reducing obesity-related risks.
How similar studies have performed: Other studies have shown promise with family-based interventions for weight loss, indicating that this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * DYAD: Be parent/caregiver (legal parent or custodial grandparent; male or female) and child willing to participate * DYAD: Live together in the same household * PARENT/CAREGIVER: Self-identify as a racial ethic minority (i.e., black or African American or Hispanic) * PARENT/CAREGIVER: Parent or caregiver age 18 through 65 years old * PARENT/CAREGIVER: Are overweight (BMI greater than or equal to 25); * PARENT/CAREGIVER: Are not currently participating in a physical activity (PA), diet, or weight management program * PARENT/CAREGIVER: Have a valid home address, telephone number, and internet access * PARENT/CAREGIVER: Enroll with a child aged 8-17 years * PARENT/CAREGIVER: Are able to speak English Exclusion Criteria: * PARENT/CAREGIVER: They are currently pregnant or thinking about becoming pregnant during the study period * PARENT/CAREGIVER: They present any contraindications for exercise based on responses to the PA Readiness Questionnaire plus (PAR-Q +) Exclusion criteria for child: 1) None.
Where this trial is running
Houston, Texas
- M D Anderson Cancer Center — Houston, Texas, United States (Recruiting)
Study contacts
- Principal investigator: Lorna McNeill — M.D. Anderson Cancer Center
- Study coordinator: Lorna McNeill
- Email: lmcneill@mdanderson.org
- Phone: 713-563-1103
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.