Prevention of Weight Gain
2 other identifiers
interventional
N/A
1 country
1
Brief Summary
The purpose of this study is to test methods for preventing weight gain in normal-weight and overweight women aged 25 through 44. Participants will complete brief questionnaires about their health, eating and exercise habits, and use of weight control strategies. They will then be randomly assigned to 1 of 3 treatment conditions. All 3 treatments receive information on the importance of maintaining a healthy body weight, the components of a healthy diet, and ways to increase activity levels. The 3 treatment differ in how this information is delivered. At 12, 24 and 36 months after enrolling in the study, participants will attend assessment sessions. They will complete questionnaires and have body weight measured.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Feb 2001
Shorter than P25 for not_applicable obesity
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2001
CompletedFirst Submitted
Initial submission to the registry
February 9, 2001
CompletedFirst Posted
Study publicly available on registry
February 9, 2001
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2001
CompletedJanuary 14, 2010
January 1, 2010
February 9, 2001
January 12, 2010
Conditions
Keywords
Interventions
Eligibility Criteria
You may qualify if:
- Body mass index of 21 through 30
You may not qualify if:
- Presence of chronic disease that precludes regular physical activity or changes in dietary intake
- Currently receiving treatment for psychological disorder
- Currently pregnant or having given birth within last 12 months
- Use in last 3 months of weight loss medications or other drugs that affect body weight
- Participation in a weight loss program in last 12 months
- Planning to relocate outside the study area in the next 3 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Pittsburgh School of Medicine
Pittsburgh, Pennsylvania, 15213, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Sponsor Type
- NIH
Study Record Dates
First Submitted
February 9, 2001
First Posted
February 9, 2001
Study Start
February 1, 2001
Study Completion
December 1, 2001
Last Updated
January 14, 2010
Record last verified: 2010-01