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Clinical Trial: Individualized Exercise Program for Treatment of Fatigue in Patients After HSCT.
This study is currently recruiting patients.
Verified by Alberta Cancer Board September 2005
Purpose
Investigates impact of a monitored program in kinesiology lab at the University of Calgary on fatigue in severely affected transplant patients.
| Condition | Intervention |
|---|---|
| Malignant disease Transplant | Behavior: exercise |
MedlinePlus consumer health information
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Individualized Exercise Program for Treatment of Fatigue in Patients After Hematalogic Stem Cell Transplant.
Further Study Details:
Primary Outcomes: Fatigue score
Expected Total Enrollment: 24
Expected Total Enrollment: 24
Study start: April 2003; Expected completion: December 2010
Last follow-up: December 2010; Data entry closure: December 2010
Investigates impact of a monitored program in kinesiology lab at the University of Calgary on fatigue in severely affected transplant patients.
Eligibility
Ages Eligible for Study: 18 Years - 70 Years, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
- severe fatigue post transplant
Exclusion Criteria:
- other conditions contributing to fatigue (graft versus host disease)
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00156871
James Russell, FRCP 403-521-3706
Canada, Alberta
Tom Baker Cancer Centre, Calgary, Alberta, T2N 4N2, Canada; Recruiting
Rachel Syme, PhD clinical_trials_tbcc@cancerboard.ab.ca
Study chairs or principal investigators
James Russell, Principal Investigator, Alberta Cancerboard
More Information
Study ID Numbers: 181710-DRD 16; ACF 717905155
Last Updated: September 10, 2005
Record first received: September 8, 2005
ClinicalTrials.gov Identifier: NCT00156871
Health Authority: Canada: Health Canada
ClinicalTrials.gov processed this record on 2005-09-13
Last Updated: September 10, 2005
Record first received: September 8, 2005
ClinicalTrials.gov Identifier: NCT00156871
Health Authority: Canada: Health Canada
ClinicalTrials.gov processed this record on 2005-09-13
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