Family-Focused text program aims to curb childhood obesity in hispanic communities
NCT ID NCT07144800
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a family-centered program to help Hispanic families lose weight and prevent obesity. About 1,319 parents and their children ages 8-12 will take part. The program uses text messages and family support to encourage healthy eating and activity.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 1,319 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2025
- Expected to finish
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Jul 2031
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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) * 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) 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) * For women, is lactating (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 physical activity restrictions, i.e., handicapped or mobility issues, that may affect physical activity participation (increasing step counts; 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 (child participant) * Has dietary restrictions, i.e., liquid diet, that may affect diet and study participation (per parent self-report) * Has physical activity restrictions, i.e., handicapped or mobility issues, that may affect physical activity participation (per parent self-report) * Has an eating disorder (per parent self-report) * Is underweight (per parent self-report)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Memorial Sloan Kettering Cancer Center (All Protocol Activities)
RECRUITINGNew York, New York, 10065, United States
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