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Web-Based Active Balance Childhood Study in Chinese-American

Web-Based Active Balance Childhood Study in Chinese-American (Web ABC Study): A Randomized Clinical Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00961246
Acronym
WEBABC
Enrollment
70
Registered
2009-08-18
Start date
2008-03-31
Completion date
2009-05-31
Last updated
2013-09-25

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

Conditions

Healthy

Keywords

web based intervention, individually-tailored, Chinese-American children, compared the changes in physical activity level, changes in dietary intake, changes in coping strategy used, changes in BMI

Brief summary

This study compares the feasibility and efficacy of an individually tailored, child-centered, Internet-based behavioral intervention with that of general Internet-based health information for improving health behaviors and relative weight in Chinese-American children during a 6-month period. A total of 60 children (age 10-14) and their families will be randomized to either the intervention group or control group. The intervention is based on the Social Cognitive Theory and Transtheoretical Model.

Detailed description

The proposed study will use a randomized experimental design to examine the effects of an individually tailored, Internet-based behavioral intervention program on improving health behavior (dietary intake and physical activity) and anthropometrics of Chinese-American children. A total of 60 children and their families will be recruited. The intervention will include a weekly Internet session tailored to each individual child for eight weeks and three Internet sessions for parents. Children and their parents in the control group will receive general health information on healthy eating, active lifestyles, dental care, smoking cessation, and risk taking issues via the Internet. The content of the sessions is described later. After informed consent is obtained from parents and verbal assent from the children, baseline data (T0) will be collected before assigning the children and parents to the intervention group or control group. Follow-up data for both groups will be collected at 2 months (T1), 4 months (T2) and 6 months (T3) after baseline.

Interventions

participants received general health information

BEHAVIORALindividually-tailored intervention

participants received individually-tailored intervention

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
10 Years to 14 Years
Healthy volunteers
Yes

Inclusion criteria

Children: * children between the ages of 10 and 14 years old who self-identify as Chinese or of Chinese origin * reside in the Bay Area in the same household as at least one parent, can read and speak English, and have access to the Internet at home Parents: * parents who self-identify as Chinese or of Chinese origin * have children between the ages of 11 and 14 * are able to read either Chinese or English * are able to speak Mandarin, Cantonese, or English * have access to the Internet at home

Exclusion criteria

* children with chronic health problems that include any dietary modifications or activity limitations will be excluded (e.g., diabetes, exercise-induced asthma)

Design outcomes

Primary

MeasureTime frame
BMIbaseline to 6 month follow up

Secondary

MeasureTime frame
physical activity, dietary intake, coping strategybaseline to 6 month follow up

Countries

United States

Outcome results

None listed

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