Prevention of Weight Gain
Primary Purpose
Obesity, Body Weight Changes
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Weight Gain Prevention for Women Project
Sponsored by
About this trial
This is an interventional prevention trial for Obesity focused on measuring weight gain
Eligibility Criteria
Inclusion Criteria: Body mass index of 21 through 30 Exclusion Criteria: 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
Sites / Locations
- University of Pittsburgh School of Medicine
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00011102
First Posted
February 9, 2001
Last Updated
January 12, 2010
Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
1. Study Identification
Unique Protocol Identification Number
NCT00011102
Brief Title
Prevention of Weight Gain
Official Title
Prevention of Weight Gain in Women Aged 25 Through 44
Study Type
Interventional
2. Study Status
Record Verification Date
January 2010
Overall Recruitment Status
Completed
Study Start Date
February 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2001 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
4. Oversight
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Body Weight Changes
Keywords
weight gain
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Allocation
Randomized
8. Arms, Groups, and Interventions
Intervention Type
Behavioral
Intervention Name(s)
Weight Gain Prevention for Women Project
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
44 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Body mass index of 21 through 30
Exclusion Criteria:
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
Facility Information:
Facility Name
University of Pittsburgh School of Medicine
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Prevention of Weight Gain
We'll reach out to this number within 24 hrs