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NCT00156871 Clinical Trial

Individualized Exercise Program for Treatment of Fatigue in Patients After Hematologic Stem Cell Transplant (HSCT)

Fatigue Clinical Trial

Official title:
Individualized Exercise Program for Treatment of Fatigue in Patients After Hematologic Stem Cell Transplant

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00156871
Other study ID # 181710-DRD 16
Secondary ID ACF 717905155
Status Completed
Phase N/A
First received September 8, 2005
Last updated January 18, 2012
Start date April 2003
Est. completion date December 2005

Study information
Verified date August 2011
Source AHS Cancer Control Alberta
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the impact of fatigue in severely affected transplant patients.

Description:

Investigates impact of a monitored program in kinesiology lab at the University of Calgary on fatigue in severely affected transplant patients.

Recruitment information / eligibility
Status Completed
Enrollment 24
Est. completion date December 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Severe fatigue post transplant

Exclusion Criteria:

- Other conditions contributing to fatigue (graft versus host disease)

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• exercise

Locations
Country Name City State
Canada Tom Baker Cancer Centre Calgary Alberta

Sponsors (2)
Lead Sponsor Collaborator
Alberta Health Services Alberta Cancer Foundation

Country where clinical trial is conducted

Canada, 

Outcome
Type Measure Description Time frame Safety issue
Primary Fatigue score
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