Exercise for Seniors |
Seniors' Fitness |
Clinical Trial: Bone Development in Adolescent Girls: Effects of Calcium and Exercise
This study is no longer recruiting patients.
|
Purpose
Osteoporosis is a major public health problem. Prevention of osteoporosis depends in part on good bone development in childhood and adolescence. This study will evaluate a weight-bearing exercise program and high-calcium diet on bone development in adolescent girls.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Osteoporosis | Behavior: Calcium rich diet Behavior: Weight bearing exercise | Phase I Phase II |
MedlinePlus related topics: Osteoporosis
Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Active Control, Factorial Assignment, Efficacy Study
Official Title: Calcium and Exercise Effect on Pubertal Bone Gain
Expected Total Enrollment: 107
Study start: May 1998
There are currently few safe and effective methods for restoring lost bone to the osteoporotic skeleton. Therefore, prevention of osteoporosis is crucial. If skeletal development can be maximized during growth, young people will begin adulthood with optimal bone mass and will be less likely to develop osteoporosis in later years. This study will determine the effects of weight-bearing physical activity and a high-calcium diet on bone mass in adolescent girls.
Participants in this study will be randomized to one of three study arms. Girls in Arm 1 will consume their usual diets and will participate in a weight-bearing exercise program that meets 3 times per week. Girls in Arm 2 will also participate in a weight-bearing exercise program that meets 3 times per week and will be given high calcium foods to supply 1500 mg of calcium per day. Girls in Arm 3 will consume their usual diet and maintain their customary activity level. Study visits occur every 6 months; participants will be followed for 4 ½ years. Assessments will include a medical and social history and measurements of spine, hip, radius, and total body bone mineral content (BMC); calcaneal speed of sound (SOS); height; weight; and Tanner stage.
Eligibility
Ages Eligible for Study: 9 Years - 10 Years, Genders Eligible for Study: Female
Accepts Healthy Volunteers
Criteria
Inclusion Criteria
Exclusion Criteria
- History of lactose intolerance, milk allergy, corticosteroid or anticonvulsant therapy, familial hypercholesterolemia, mental or physical handicaps, cancer, rheumatoid arthritis, asthma, or any other significant health problem
- Body mass index (BMI) >= 85th percentile for age and gender
- Regularly have more than two practice sessions per week of dance, gymnastics, or organized team sports
Location Information
Nebraska
Creighton University, Omaha, Nebraska, 68131, United States
Joan M. Lappe, Ph.D., Principal Investigator, Creighton University
More Information
Click here for more information about Osteoporosis research at Creighton University.
Record last reviewed: May 2003
Last Updated: October 13, 2004
Record first received: June 19, 2003
ClinicalTrials.gov Identifier: NCT00063011
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 8, 2005

Not Signed In -


