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Clinical Trials/NCT00156871
NCT00156871CompletedNot Applicable

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

Alberta Health services1 site in 1 country24 target enrollmentStarted: April 1, 2003Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
24
Locations
1
Primary Endpoint
Fatigue score
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

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

Detailed Description

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

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Severe fatigue post transplant

Exclusion Criteria

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

Outcomes

Primary Outcomes

Fatigue score

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other

Study Sites (1)

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