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HomeTech Healthy Lifestyle Program for Mothers With Young Children

Home-based & Technology-centered Childhood Obesity Prevention for Mothers With Young Children

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01819987
Enrollment
32
Registered
2013-03-28
Start date
2014-01-31
Completion date
2016-06-01
Last updated
2017-05-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overweight

Keywords

Overweight, mother, childhood obesity prevention, Chinese American

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.

Interventions

BEHAVIORALTablet computer

Participants 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.

BEHAVIORALMailing information

Participants in the control 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.

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

Participants, investigator and outcome assessor were blinded to the group assignment.

Intervention model description

A randomized, controlled study was used. The intervention group received tablet based intervention and the control group received printed health information relevant to preschool-aged children in Chinese over the eight weeks.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Exclusion criteria

* Have acute or chronic conditions that prevent performing daily activities

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline body mass index at 5 monthsBaseline and at 5 monthsParticipants 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

MeasureTime frameDescription
Change from Baseline Sedentary activity at 2 monthsbaseline and 2 monthsParticipants 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 monthsParticipants 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 Self-efficacy regarding diet and physical activity at 2 monthsbaseline and 2 monthsParticipants 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 at 2 monthsBaseline and 2 monthsParticipants 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 Sedentary activity at 5 monthsbaseline and 5 monthsParticipants will complete Family Eating and Activity Habits Questionnaire at baseline and at 5 months.
Change from Baseline Parental Feeding Practice at 5 monthsbaseline and 5 monthsParticipants will complete Child Feeding Questionnaire at baseline and at 5 months . Change of parental feeding practice from baseline will be assessed at 5 months.
Change from Baseline Self-efficacy regarding diet and physical activity at 5 monthsbaseline and 5 monthsParticipants 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 physical activity level at 5 monthsBaseline and 5 monthsChange in baseline physical actiivty level will be measured at 5 months.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026