MedPath

HomeTech Healthy Lifestyle Program for Mothers With Young Children

Phase 1
Completed
Conditions
Overweight
Interventions
Behavioral: Mailing information
Behavioral: Tablet computer
Registration Number
NCT01819987
Lead Sponsor
University of California, San Francisco
Brief Summary

About 17% of Chinese American preschool children are obese, compared to 12.4%of all children from age three to five years residing in the US; the prevalence of obesity is expected to increase in the future. Therefore, the proposed study will adapt a home-based and technology-centered childhood obesity prevention program for low-income Chinese American mothers of children three to five years old. The aims of the study are to assess the feasibility of the intervention and estimate the effect sizes on children's and mothers' outcomes.

Detailed Description

This study aims to adapt and implement a family-centered and technology-based intervention to prevent obesity in young Chinese American children from low-income families with overweight mothers. The proposed study framework is based on the Information Motivation Behavioral Skills Model, which includes the mothers' gained knowledge/information, increased personal and social motivators, and acquired behavioral skills towards behavioral changes. The intervention will be developed with a Community Advisory Committee and validated for cultural appropriateness through a beta-testing process. The validated intervention will be implemented thereafter. Eligible overweight mothers with young Chinese American children (ages three to five years) will be recruited from local day care settings, low-income housing and Head Start programs to participate in the study. Participants will be randomized into either the intervention (N=15) or control group (N=15). Participants in the intervention group will receive the 8-week online interactive sessions and activities delivered through tablet computers. Participants in the control group will receive general health promotion topics relevant to preschool-age children via mailing materials weekly for eight weeks.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
32
Inclusion Criteria
  • Children:
  • must be between ages three and five
  • have a mother who identifies her child as Chinese;
  • be healthy-defined as free of chronic or acute illness.
  • Mothers:
  • must identify themselves as Chinese
  • the primary provider of the child,
  • be able to speak and read Chinese or English;
  • with a BMI >= 23.0;
  • meet low-income requirements in the Bay Area.
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Exclusion Criteria
  • Have acute or chronic conditions that prevent performing daily activities
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Mailing informationMailing informationParticipants in the mailing information group will receive general health promotion topics relevant to preschool-age children (such as immunization, injury prevention and school readiness) via mailing materials that are bilingual weekly for eight weeks. These materials will be obtained from CDC and AAP.
Tablet computerTablet computerParticipants in the intervention group will receive eight weekly online sessions and interactive activities delivered through tablet computers. Intervention participants will receive instructions for accessing the program via the tablet at an in-person session. Automated weekly emails will be sent to participating mothers for the intervention duration to encourage study engagement.
Primary Outcome Measures
NameTimeMethod
Change from Baseline body mass index at 5 monthsBaseline and at 5 months

Participants will have their weight and height measured and body mass index will be calculated. Change of BMI from baseline will be assessed at 5 months post baseline

Secondary Outcome Measures
NameTimeMethod
Change from Baseline Sedentary activity at 2 monthsbaseline and 2 months

Participants will complete Family Eating and Activity Habits Questionnaire at baseline and at 2 month.

Change from Baseline Parental Feeding Practice at 2 monthsbaseline and 2 months

Participants will complete Child Feeding Questionnaire at baseline and at 2 months . Change of parental feeding practice from baseline will be assessed at 2 months.

Change from baseline physical activity at 2 monthsBaseline and 2 months

Participants will wear Actigraphy for 7 days at baseline and at 2 months. Change of physical activity from baseline will be assessed at 2 months post baseline.

Change from Baseline Self-efficacy regarding diet and physical activity at 5 monthsbaseline and 5 months

Participants will complete self-efficacy questionnaire regarding nutrition and physical behavior at baseline and at 5 months. Change of self-efficacy from baseline will be assessed at 5 months.

Change from Baseline Sedentary activity at 5 monthsbaseline and 5 months

Participants will complete Family Eating and Activity Habits Questionnaire at baseline and at 5 months.

Change from Baseline Self-efficacy regarding diet and physical activity at 2 monthsbaseline and 2 months

Participants will complete self-efficacy questionnaire regarding nutrition and physical behavior at baseline and at 2 months. Change of self-efficacy from baseline will be assessed at 2 months.

Change from baseline physical activity level at 5 monthsBaseline and 5 months

Change in baseline physical actiivty level will be measured at 5 months.

Change from Baseline Parental Feeding Practice at 5 monthsbaseline and 5 months

Participants will complete Child Feeding Questionnaire at baseline and at 5 months . Change of parental feeding practice from baseline will be assessed at 5 months.

Trial Locations

Locations (1)

University of California San Francisco

🇺🇸

San Francisco, California, United States

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