Osteoporosis |
Bone Loss |
Clinical Trial: Program to Prevent Osteoporosis in Girls
This study is no longer recruiting patients.
|
Purpose
Osteoporosis is a condition defined by decreased bone mass. Osteoporosis generally affects older women and can lead to bone fractures. One way to prevent osteoporosis is to build strong, healthy bones during childhood. This study will evaluate a program designed to improve girls' bones. The program encourages eating foods rich in calcium and participating in physical activity.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Osteoporosis | Behavior: Increased calcium intake Behavior: Weight-bearing physical activity | Phase III |
MedlinePlus related topics: Osteoporosis
Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Active Control, Factorial Assignment, Efficacy Study
Official Title: Behavioral Strategies to Prevent Osteoporosis in Girls
Expected Total Enrollment: 322
Study start: June 1999; Study completion: May 2004
Osteoporosis affects more than 25 million people in the United States. The majority of bone fractures in older women are related to osteoporosis. Calcium intake and physical activity are two modifiable behaviors associated with peak bone mass. Interventions targeting these behaviors among youth have tremendous public health potential for preventing osteoporosis. This study will assess the feasibility and effectiveness of a 2-year behavioral program designed to increase calcium intake and physical activity among girls ages 9 to 11.
Thirty Girl Scout troops will be recruited for the study. Girls will be randomized either to the eating and exercise behavior change program or to a control group. Program components focus on behavioral skills development, goal setting, and self-monitoring for dietary calcium intake and physical activity. The program also works to increase social support from peers and parents. The program will take place during 10 weeks of both the 5th and 6th grade years. The program also includes supporting programs during winter and summer breaks. Outcome assessments will be conducted at baseline, and at 6, 12, and 24 months. Primary outcomes will include dietary calcium intake, physical activity, and bone mineral density.
Eligibility
Ages Eligible for Study: 9 Years - 11 Years, Genders Eligible for Study: Female
Accepts Healthy Volunteers
Criteria
Inclusion Criteria
- Member of a Girl Scout troop with at least eight 5th grade girls
- Member of the Greater Minneapolis or St. Croix Valley Girl Scout organization
- Only troops with unanimous parental consent will be included in the trial
Location Information
Minnesota
Division of Epidemiology, School of Public Health, University of Minnesota, Minneapolis, Minnesota, 55454-1015, United States
Simone A. French, Ph.D., Principal Investigator, University of Minnesota
More Information
Record last reviewed: May 2003
Last Updated: October 13, 2004
Record first received: June 19, 2003
ClinicalTrials.gov Identifier: NCT00063024
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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