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Family COMIDA (Consumo de Opciones Más Ideales De Alimentos) (Eating More Ideal Food Options) | Clinical Trials | Clareo Health

RECRUITINGNA

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

NCT07144800•Memorial Sloan Kettering Cancer Center

View on ClinicalTrials.gov

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

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•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)
+11 more criteria

Exclusion Criteria

•Phase 1
•Is pregnant or might be pregnant (per self-report)
•Presence of a chronic disease such as cancer, kidney disease, liver disease, etc. (individuals with hypertension and diabetes mellitus may still participate) that may affect diet and study participation (per self-report)
•Has dietary restrictions, i.e. liquid diet, that may affect diet and study participation (per self-report)
•Has a household member who has already participated or agreed to participate in this study program (per self-report)
•Prior participation in one of our preliminary studies, e.g., COMIDA, SANOS, Family COMIDA (per self-report) and any related focus groups
•Works for or with the VDS or MHU (per self-report)
•Presence of cognitive impairment disorder (i.e., delirium or dementia) sufficient to preclude meaningful informed consent and/or data collection (per study team)
•Phase 2 (parent participant)
•Is pregnant or might be pregnant (per self-report)
+13 more criteria

Locations (1)

Memorial Sloan Kettering Cancer Center (All Protocol Activities)

New York, New York, United States

Key Dates

Start Date

August 22, 2025

Primary Completion Date

July 31, 2030

Completion Date

July 31, 2031

Last Updated

February 2, 2026

Enrollment

1,319

ESTIMATED participants

Conditions

ObesityChild ObesityWeight Loss

Interventions

Parent Weekly Individual Telephone Support

BEHAVIORAL

Child Education

BEHAVIORAL

Parent Initial Counseling

BEHAVIORAL

Parent Monthly Group Support

BEHAVIORAL

Contacts

Jennifer Leng, MD, MPH

CONTACT

646-888-8057 lengj@mskcc.org

Francesca Gany, MD, MS

CONTACT

646-888-8054 ganyf@mskcc.org

Multi-Acupoint Laser Therapy for Body Shape and Composition in Obese Menopausal Women

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: February 2, 2026Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions

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

Inclusion Criteria

Exclusion Criteria

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