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

Part of paid clinical trials in New York, New York.

Sponsor
Memorial Sloan Kettering Cancer Center
Study ID
NCT07144800
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Parent Weekly Individual Telephone Support — BEHAVIORAL
    Interventionists will deliver a 20-30 minute session via videoconference (e.g. Zoom) using the Family COMIDA Intervention Manual
  • Child Education — BEHAVIORAL
    6 weekly diet/PA education sessions ('Child Education')
  • Parent Initial Counseling — BEHAVIORAL
    Interventionists will deliver a 20-30 minute session via videoconference (e.g. Zoom) using the Family COMIDA Intervention Manual
  • Parent Monthly Group Support — BEHAVIORAL
    Parents will be invited to join a Spanish language (English if preferred) weekly group videoconference (can join by phone if preferred).

Study Details

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.

Key Dates

Start date
Aug 22, 2025
Status verified
Apr 2026
Primary completion
Jul 31, 2030
Completion
Jul 31, 2031

Study Design

Enrollment
1,319 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION

Arms

  • 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

Primary Outcome Measure

Percentage weight loss from baseline among participants [ Time Frame: 6 months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Memorial Sloan Kettering Cancer Center (All Protocol Activities)New YorkNew York10065
Jennifer Leng, MD, MPH
646-888-8057

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