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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02273024
Other study ID # 14-7699
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2014
Est. completion date August 2019

Study information

Verified date November 2019
Source University Health Network, Toronto
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators hypothesize that inactivity during the search for a donor may exacerbate current deconditioned states; subsequently, influencing risk factors for post-transplant complications that hinder the recovery phase.

This study is designed to investigate if exercise therapy administered prior to allogeneic hematologic stem cell transplantation (HSCT) can influence physical and psychological side-effects associated with HSCT. Approximately 6-weeks prior to HSCT, individuals will be randomized into either an exercise group or usual care group and followed until one year after HSCT.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date August 2019
Est. primary completion date August 2019
Accepts healthy volunteers No
Gender All
Age group 17 Years and older
Eligibility Inclusion Criteria:

- Medical indication: allogeneic stem cell transplantation at Princess Margaret Hospital

- must be ambulatory without need for human assistance at time of recruitment

- medically cleared to exercise by the transplant physician

- demonstrates willingness to attend supervised sessions

- sufficient in English to ensure safety of understanding prescribed exercise guidelines, or has access to an adequate non-familial interpreter

Exclusion Criteria:

- another active malignancy

- less than 4 weeks till the scheduled HSCT

- refusal to be randomized

- does not have the approval of their transplant physician

- severe or unstable neurological, cardiorespiratory, musculoskeletal disease or mental illness

Study Design


Related Conditions & MeSH terms

  • Allogeneic Stem Cell Transplantation

Intervention

Behavioral:
Exercise


Locations

Country Name City State
Canada Princess Margaret Hospital & Toronto Rehabilitation Institute Toronto Ontario

Sponsors (3)

Lead Sponsor Collaborator
University Health Network, Toronto Princess Margaret Hospital, Canada, Toronto Rehabilitation Institute

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Adherence to exercise sessions Feasibility of an exercise intervention prior to HSCT till T100 One year
Primary Change in Physical Function Cardiopulmonary Capacity (VO2peak) Baseline, 1 week pre HSCT, T100, 1yr post HSCT
Secondary Change in Quality of Life European Organization for Research and Treatment of Cancer (EORTC) core 30-item questionnaire (QLQ-30) Baseline, 1 week pre HSCT, T100, 1yr post HSCT
Secondary Change in Symptoms Memorial Symptom Assessment Scale (MSAS) Baseline, 1 week pre HSCT, T100, 1yr post HSCT
Secondary Change in Anxiety The Generalized Anxiety Disorder (GAD7) Baseline, 1 week pre HSCT, T100, 1yr post HSCT
Secondary Change in Depression The Patient Health Questionnaire (PHQ-9), will be used as a clinically relevant measure to evaluate depression Baseline, 1 week pre HSCT, T100, 1yr post HSCT
Secondary Change in Fatigue Multidimensional Fatigue Inventory Baseline, 1 week pre HSCT, T100, 1yr post HSCT
Secondary Change in Treatment Side-effects Hospitalization (days till discharge and readmission rates), bone marrow engraftment (days), graft versus host disease incidence (acute & chronic), severity of diarrhea/ vomiting/ nausea, infections, steroid use, blood counts Baseline, 1 week pre HSCT, T100, 1yr post HSCT
Secondary Change in Strength upper body: grip strength; lower body: chair-stand test Baseline, 1 week pre HSCT, T100, 1yr post HSCT
Secondary Change in Six-minute walk test Baseline, 1 week pre HSCT, T100, 1yr post HSCT
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