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NCT00619047 Clinical Trial

The Role of Impact Activity in Peripubertal Bone Accrual

Bone Mineral Density Clinical Trial

Official title:
The Role of Impact Activity in Peripubertal Bone Accrual

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00619047
Other study ID # Bone Density Study
Secondary ID
Status Completed
Phase N/A
First received February 6, 2008
Last updated November 18, 2009
Start date January 2002
Est. completion date August 2008

Study information
Verified date November 2009
Source State University of New York - Upstate Medical University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Osteoporosis has been established as a major public health problem, primarily effecting women. The attainment of maximal peak bone mass is crucial in the prevention of osteoporosis, yet little is known about the specifics of bone accrual. Physical activity has been identified as an important modifiable factor controlling bone accrual. It is has been shown that increased activity during peri-pubertal years increase bone mineral content during adulthood. Thus, strategies designed to increase peak bone mass should target the peri-pubertal years of critical bone acquisition.

Hypothesis 1a: The amount of bone mineral accrued during the peri-pubertal years is greater in girls who engage in impact activity than in those who do not.

Hypothesis 1b: The positive effects of impact activity on bone accrual are maintained after cessation of the activity, resulting in greater bone mineral density in girls who participate in impact activity during a portion of the peri-pubertal years than in those who never participated in impact activity.

Description:

As above

Recruitment information / eligibility
Status Completed
Enrollment 131
Est. completion date August 2008
Est. primary completion date August 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 10 Years to 12 Years
Eligibility Inclusion Criteria:

- Subjects between the ages of 10-12 will be asked to participate

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Institute for Human Performance Syracuse New York

Sponsors (1)
Lead Sponsor Collaborator
State University of New York - Upstate Medical University

Country where clinical trial is conducted

United States, 

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