Clinical trial
Parent and Family Obesity Intervention in Reducing Obesity Risk in Racial Ethnic Minority Families
Active, not recruiting · Not applicable · 1 countries · Registry ID NCT05094466
Active, not recruitingNot applicableInterventional
What this study is about
This clinical trial compares the effects of parent/caregiver-focused programs to family-focused programs in reducing obesity risk in racial ethnic minority families. Obesity tends to run in families, thus family-based interventions have been strongly recommended. Parent and family obesity programs may reduce obesity risk and ultimately reduce the risk of obesity-related cancer.
A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.
Basic eligibility
Age10 Years to Not listed
SexAll
Healthy volunteersAccepted
ConditionObesity-Related Malignant Neoplasm
Full registry criteria
Inclusion Criteria: * ELIGIBLE IN-DEPTH INTERVIEW PARTICIPANTS: Any church leader, such as pastors, minister, church secretary, health ministry leader, youth leader, deacons, ministry leader, director * PARENT-CHILD DYADS: Be parent/caregiver (legal parent or custodial grandparent; male or female) and child willing to participate * PARENT-CHILD DYADS: Live together in the same household * PARENTS/CAREGIVERS: Self-identify as a racial ethnic minority (i.e., black or African American or Hispanic) * PARENTS/CAREGIVERS: Parent or caregiver age 18 through 65 years old * PARENTS/CAREGIVERS: Are obese (body mass index \[BMI\] \>= 30) * PARENTS/CAREGIVERS: Are not currently participating in a physical activity (PA), diet, or weight management program * PARENTS/CAREGIVERS: Enroll with a child aged 10-16 years * PARENTS/CAREGIVERS: Have a valid home address, telephone number, and internet access * PARENTS/CAREGIVERS: Are able to speak, read, and write in English * CHILDREN: They are aged between 10-16 years Exclusion Criteria: * PARENTS/CAREGIVERS: They are currently pregnant or thinking about becoming pregnant during study period * PARENTS/CAREGIVERS: They present any contraindications for exercise based on responses to the PA Readiness Questionnaire * PARENTS/CAREGIVERS: Principal investigator (PI) determines that parent/caregiver is unsuitable for the study for reasons not otherwise stated in the protocol
Treatments and study arms
Behavioral Intervention
Behavioral
Receive peer support sessions
Counseling
Other
Receive health coaching sessions
Discussion
Procedure
Attend focus groups
Educational Intervention
Other
Receive handbook
Informational Intervention
Other
Receive navigation sessions
Interview
Other
Participate in interview
Primary outcomes
The correlation between the feasibility of the Parent and Family obesity interventions.Up to 4 years
The correlation between the acceptability of the Parent and Family obesity interventions.Up to 4 years
Study locations
1 locations were listed when this page was built. The first 40 are shown.
M D Anderson Cancer Center🇺🇸 Houston, Texas, United States