Obesity in Children Clinical Trials

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Family COMIDA (Consumo de Opciones Más Ideales De Alimentos) (Eating More Ideal Food Options)

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this study is to determine the most effective family-centered intervention (FCI) for weight loss and obesity prevention in Hispanic families. FCI is a type of program that involves family (such as parents and caregivers) supporting their children to promote healthy habits.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

⁃ Phase 1

• Age \>= 18 years (per self-report)

• Self-identifies as Hispanic/Latino (per self-report)

• Seeking, or has used, services at the VDS or MHU (per self-report)

• Is the parent or primary caregiver for at least one child aged 8-12 living in their household (per self-report)

• Screens as obese (BMI \> 30 kg/m2) or overweight (BMI of 25 - 29.9 kg/m2) (per height and weight measurement in person or per self-report)

• Owns a cell phone capable of receiving text messages (per self-report)

• Owns an internet connected device (e.g. cell phone, tablet, etc.) capable of conducting videoconference calls (per self-report)

• Agrees to be audio-recorded (per self-report)

⁃ Phase 2 (parent participants)

• Age \>= 18 years (per self-report)

• Self-identifies as Hispanic/Latino (per self-report)

• Seeking, or has used, services at the VDS or MHU (per self-report)

• Is the parent or primary caregiver for at least one child aged 8-12 living in their household (per self-report)

• Screens as obese (BMI \> 30 kg/m2) or overweight (BMI of 25 - 29.9 kg/m2) (per height and weight measurement in person or remotely)

• Owns a cell phone capable of receiving text messages (per self-report)

• Owns an internet connected device (e.g. cell phone, tablet, etc.) capable of conducting videoconference calls (per self-report)

• Agrees to be audio-recorded (per self-report)

⁃ Phase 2 (child participants)

• Age 8-12 years (per parent self-report)

• Has a parent or primary caregiver who is eligible and participating in Phase 2 (per parent self-report)

Locations
United States
New York
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
RECRUITING
New York
Contact Information
Primary
Jennifer Leng, MD, MPH
lengj@mskcc.org
646-888-8057
Backup
Francesca Gany, MD, MS
ganyf@mskcc.org
646-888-8054
Time Frame
Start Date: 2025-08-22
Estimated Completion Date: 2031-07-31
Participants
Target number of participants: 1319
Treatments
Experimental: Condition 1: Tele
Intervention for 6 months more or less
Experimental: Condition 2: Child Education
Intervention for 6 months
Experimental: Condition 3: Parent Counseling
Intervention for 6 months
Experimental: Condition 4: Counseling, Child Education, and Tele
Intervention for 6 months
Experimental: Condition 5: Group Support
Intervention for 6 months
Experimental: Condition 6: Group Support, Child Education, and Tele
Intervention for 6 months
Experimental: Condition 7: Group Support, Parent Counseling, and Tele
Intervention for 6 months
Experimental: Condition 8: Group Support, Parent Counseling, and Child Education
Intervention for 6 months
Related Therapeutic Areas
Sponsors
Leads: Memorial Sloan Kettering Cancer Center

This content was sourced from clinicaltrials.gov