Musculoskeletal Outcomes After Bone Marrow Transplant

This study has been completed.
Sponsor:
Information provided by:
Sidney Kimmel Comprehensive Cancer Center
ClinicalTrials.gov Identifier:
NCT00558948
First received: November 14, 2007
Last updated: August 18, 2009
Last verified: August 2009

November 14, 2007
August 18, 2009
May 2007
August 2009   (final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT00558948 on ClinicalTrials.gov Archive Site
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Musculoskeletal Outcomes After Bone Marrow Transplant
Musculoskeletal Outcomes After Bone Marrow Transplant

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.

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.

Observational
Observational Model: Case-Only
Time Perspective: Cross-Sectional
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Non-Probability Sample

Survivors of bone marrow transplant (autologous and allogeneic) who are at least 1 year from transplant.

  • Survivors of Bone Marrow Transplant
  • Autologous and Allogeneic
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
48
August 2009
August 2009   (final data collection date for primary outcome measure)

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
Both
8 Years to 30 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00558948
J06120, 1F31NR010038-01
Yes
Kathy Ruble, PhDc, RN, SKCCC
Sidney Kimmel Comprehensive Cancer Center
Not Provided
Study Director: Kathy Ruble, PhDc, RN Johns Hopkins University, School of Nursing
Sidney Kimmel Comprehensive Cancer Center
August 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP