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临床试验/NCT07144800
NCT07144800招募中不适用

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

Memorial Sloan Kettering Cancer Center1 个研究点 分布在 1 个国家目标入组 1,319 人开始时间: 2025年8月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
1,319
试验地点
1
主要终点
Percentage weight loss from baseline among participants

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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)

排除标准

  • 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)

研究组 & 干预措施

Condition 1: Tele

Experimental

Intervention for 6 months more or less

干预措施: Parent Weekly Individual Telephone Support (Behavioral)

Condition 2: Child Education

Experimental

Intervention for 6 months

干预措施: Child Education (Behavioral)

Condition 3: Parent Counseling

Experimental

Intervention for 6 months

干预措施: Parent Initial Counseling (Behavioral)

Condition 4: Counseling, Child Education, and Tele

Experimental

Intervention for 6 months

干预措施: Parent Weekly Individual Telephone Support (Behavioral)

Condition 4: Counseling, Child Education, and Tele

Experimental

Intervention for 6 months

干预措施: Child Education (Behavioral)

Condition 4: Counseling, Child Education, and Tele

Experimental

Intervention for 6 months

干预措施: Parent Initial Counseling (Behavioral)

Condition 5: Group Support

Experimental

Intervention for 6 months

干预措施: Parent Monthly Group Support (Behavioral)

Condition 6: Group Support, Child Education, and Tele

Experimental

Intervention for 6 months

干预措施: Parent Weekly Individual Telephone Support (Behavioral)

Condition 6: Group Support, Child Education, and Tele

Experimental

Intervention for 6 months

干预措施: Child Education (Behavioral)

Condition 6: Group Support, Child Education, and Tele

Experimental

Intervention for 6 months

干预措施: Parent Monthly Group Support (Behavioral)

Condition 7: Group Support, Parent Counseling, and Tele

Experimental

Intervention for 6 months

干预措施: Parent Weekly Individual Telephone Support (Behavioral)

Condition 7: Group Support, Parent Counseling, and Tele

Experimental

Intervention for 6 months

干预措施: Parent Initial Counseling (Behavioral)

Condition 7: Group Support, Parent Counseling, and Tele

Experimental

Intervention for 6 months

干预措施: Parent Monthly Group Support (Behavioral)

Condition 8: Group Support, Parent Counseling, and Child Education

Experimental

Intervention for 6 months

干预措施: Child Education (Behavioral)

Condition 8: Group Support, Parent Counseling, and Child Education

Experimental

Intervention for 6 months

干预措施: Parent Initial Counseling (Behavioral)

Condition 8: Group Support, Parent Counseling, and Child Education

Experimental

Intervention for 6 months

干预措施: Parent Monthly Group Support (Behavioral)

结局指标

主要结局

Percentage weight loss from baseline among participants

时间窗: 6 months

To utilize an optimization trial to identify the most effective, mHealth weight loss/obesity prevention FCI for Hispanic families in the U.S. 5% weight loss from baseline among overweight/obese parents (a percentage loss associated with numerous health benefits)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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