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The Role of Impact Activity in Peripubertal Bone Accrual
This study has been completed.
Sponsored by: State University of New York - Upstate Medical University
Information provided by: State University of New York - Upstate Medical University
ClinicalTrials.gov Identifier: NCT00619047
  Purpose

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.


Condition
Accrual of Bone Mineral Content

MedlinePlus related topics: Minerals
U.S. FDA Resources
Study Type: Observational
Study Design: Cohort, Prospective
Official Title: The Role of Impact Activity in Peripubertal Bone Accrual

Further study details as provided by State University of New York - Upstate Medical University:

Biospecimen Retention:   None Retained

Biospecimen Description:

Enrollment: 131
Study Start Date: January 2002
Study Completion Date: August 2008
Primary Completion Date: August 2008 (Final data collection date for primary outcome measure)
Groups/Cohorts
Observation

  Eligibility

Ages Eligible for Study:   10 Years to 12 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population

Subjects were recruited into the following three groups based on their exposure to gymnastic activity. A) control, no gymnastic activity. B)retired gymnasts, who participated at study onset, but stopped gymnastics activity during the course of the study. C) active gymnast, who continues participation in gymnastics throughout the duration of the study.

Criteria

Inclusion Criteria:

  • Subjects between the ages of 10-12 will be asked to participate
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00619047

Locations
United States, New York
Institute for Human Performance
Syracuse, New York, United States, 13210
Sponsors and Collaborators
State University of New York - Upstate Medical University
  More Information

Responsible Party: SUNY Upstate Medical University ( Tamara A. Scerpella, MD )
Study ID Numbers: Bone Density Study
Study First Received: February 6, 2008
Last Updated: December 1, 2008
ClinicalTrials.gov Identifier: NCT00619047  
Health Authority: United States: Institutional Review Board

ClinicalTrials.gov processed this record on January 16, 2009