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Musculoskeletal Outcomes After Bone Marrow Transplant

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ClinicalTrials.gov Identifier: NCT00558948
Recruitment Status : Completed
First Posted : November 16, 2007
Last Update Posted : August 19, 2009
Sponsor:
Information provided by:
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Brief Summary:
The purpose of the study is to evaluate bone mineral density and muscle strength in survivors of bone marrow transplant. Association with age, type of transplant, steroids, years since transplant, body composition, endocrinopathies, radiation, quality of life and physical activity will be explored.

Condition or disease
Survivors of Bone Marrow Transplant Autologous and Allogeneic

Detailed Description:
Bone marrow transplant survivors are at risk of diminished bone mineral density. Mechanisms and risks are not well understood. This study will help identify risks factors for developing this complication.

Study Type : Observational
Actual Enrollment : 48 participants
Observational Model: Case-Only
Time Perspective: Cross-Sectional
Official Title: Musculoskeletal Outcomes After Bone Marrow Transplant
Study Start Date : May 2007
Actual Primary Completion Date : August 2009
Actual Study Completion Date : August 2009

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Ages Eligible for Study:   8 Years to 30 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Survivors of bone marrow transplant (autologous and allogeneic) who are at least 1 year from transplant.
Criteria

Inclusion Criteria:

  • Ages 8-30 years
  • One year from transplant

Exclusion Criteria:

  • No current steroid use
  • Medical conditions that would prohibit testing
  • Neuropsychological conditions that prohibit completing questionnaires

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To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00558948


Locations
United States, Maryland
Johns Hopkins University, Bayview Campus
Baltimore, Maryland, United States, 21212
Sponsors and Collaborators
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Investigators
Study Director: Kathy Ruble, PhDc, RN Johns Hopkins University, School of Nursing

Responsible Party: Kathy Ruble, PhDc, RN, SKCCC
ClinicalTrials.gov Identifier: NCT00558948     History of Changes
Other Study ID Numbers: J06120
1F31NR010038-01 ( U.S. NIH Grant/Contract )
First Posted: November 16, 2007    Key Record Dates
Last Update Posted: August 19, 2009
Last Verified: August 2009

Keywords provided by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins:
Bone Marrow Transplant
Bone Mineral Density
Survivors
Muscle Strength