Viewing Study NCT00961246



Ignite Creation Date: 2024-05-05 @ 9:47 PM
Last Modification Date: 2024-10-26 @ 10:09 AM
Study NCT ID: NCT00961246
Status: COMPLETED
Last Update Posted: 2013-09-25
First Post: 2009-08-16

Brief Title: Web-Based Active Balance Childhood Study in Chinese-American
Sponsor: University of California San Francisco
Organization: University of California San Francisco

Study Overview

Official Title: Web-Based Active Balance Childhood Study in Chinese-American Web ABC Study A Randomized Clinical Trial
Status: COMPLETED
Status Verified Date: 2013-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: WEBABC
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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
KL2RR024130 NIH None httpsreporternihgovquickSearchKL2RR024130