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Effects of Exercise on Allogeneic Stem Cell Transplant (Ex-BMT)

Primary Purpose

Hematological Malignancy

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Exercise
Sponsored by
Raewyn Broady
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Hematological Malignancy focused on measuring Bone Marrow Transplantation, Exercise, Rehabilitation, Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients undergoing allogeneic stem cell transplantation (including related, unrelated, cord blood or haploidentical allogeneic transplant) for any indication through the Leukemia/BMT Program of British Columbia.
  2. Age greater than or equal to 18 years.
  3. Able to provide written informed consent.

Exclusion Criteria:

  1. Severe cardiac disease including symptomatic congestive heart failure (New York Heart Association Class III or IV), unstable angina pectoris, or an unstable cardiac arrhythmia.
  2. Orthopedic illness which limits ability to conduct aerobic exercise (walking or biking).
  3. Not meeting eligibility criteria to proceed with allogeneic stem cell transplantation as per the Leukemia/BMT Program of BC.

Sites / Locations

  • Vancouver General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Exercise Group

Control Group

Arm Description

Patients in the intervention group will receive supervised and unsupervised exercise program after their bone marrow transplant.

Patient will receive standard of care within the hospital as an inpatient and outpatient after their bone marrow transplant.

Outcomes

Primary Outcome Measures

Change in Quality of Life
European Organization for Research and Treatment of Cancer Quality of Life Questionnaire. To investigate if a partially supervised exercise intervention in alloHSCT patients will result in differences in quality of life at Day 100 post transplant compared to the standard of care control group.

Secondary Outcome Measures

Changes in Quality of Life
EuroQol (EQ)-5 Dimensions (5D) -3 Level (3L) Questionnaire.
Changes in Grip Strength
Using a handheld dynamometer, measured in kg.
Changes in 30-Second Chair Stand
Number of chair stands one can perform in 30 seconds.
Changes in 6-Minute Walk Test
Distance (meters) someone can walk in 6 minutes between two cones separated by 30 meters.
Changes in Timed Up and Go
Time taken for someone to stand up from a chair, walk 3 meters, turn around, walk back to the chair, and sit sound.
Changes in Exercise Capacity
Exercise Treadmill Test via Bruce or Modified Bruce Protocol. METs and estimated peak oxygen uptake (VO2) will be determined.
Changes in Cardiopulmonary Function
Left ventricular ejection fraction vs radionuclide ventriculography (MUGA) or echocardiography.
Changes in Physical Activity Levels - Accelerometry
Accelerometry counts converted minutes/week of moderate-to-vigorous activity and sedentary activity and METS. Godin Leisure-Time Exercise Questionnaire.
Changes in Physical Activity Levels - Questionnaire
Godin Leisure-Time Exercise Questionnaire. Total leisure activity score is calculated.
Changes in Body Composition Analysis
Height (cm), weight (m), and waist/hip circumference (cm) will be measured.
Changes in Bone Mineral Density Analysis
Bone mineral density testing will be performed using a Dual-Energy X-Ray Absorptiometry (DXA).
Changes in Immune Biomarkers
A collective blood test will be done to determine the composition of white blood cells (total, lymphocytes, and subsets of T-Lymphocytes).

Full Information

First Posted
August 14, 2016
Last Updated
September 9, 2016
Sponsor
Raewyn Broady
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1. Study Identification

Unique Protocol Identification Number
NCT02900768
Brief Title
Effects of Exercise on Allogeneic Stem Cell Transplant
Acronym
Ex-BMT
Official Title
Evaluating Effects on Quality of Life of a Partially Supervised Exercise Program Following Allogeneic Stem Cell Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
September 2016
Overall Recruitment Status
Unknown status
Study Start Date
September 2016 (undefined)
Primary Completion Date
December 2020 (Anticipated)
Study Completion Date
December 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Raewyn Broady

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Although allogeneic haematopoietic stem cell transplant (AlloHSCT) is a curative treatment option for malignant hematological diseases, it is also associated with significant morbidity such as graft versus host disease, infections, and immune complications. Moreover, long-term survivors are likely to have reduced physical performance and functioning due to deconditioning, sarcopenia, and bone loss, and particularly high levels of fatigue and psycho-social stress, all of which negatively impact patients' quality of life. Purpose: To conduct a randomized controlled, single site trial investigating whether a partially supervised exercise intervention in the first 100 days post alloHSCT patients will result in improved quality of life at Day 100 post-transplant compared to standard of care treatment. Secondary objectives will investigate the effect of an exercise intervention on muscle strength, cardiorespiratory fitness, mobility, bone mineral density, body composition, exercise, and immunological/inflammatory biomarkers compared to standard of care. Procedure: 120 patients receiving alloHSCT will be baseline tested, and then randomized into an Exercise Intervention Group or Standard of Care Control Group.
Detailed Description
This is a randomized non-blinded single centre prospective clinical trial designed to evaluate the efficacy and safety of a partially-supervised progressive exercise intervention among patients undergoing alloHSCT compared to a self-directed exercise program. Approximately 120 patients will be enrolled. Following completion of all baseline data collection, participants will be randomized 1:1 to the intervention group or the control group. Patients in the intervention group will receive an exercise manual with background information, descriptions for different resistance and aerobic exercises, and instructions for tailoring the intensity of exercise. All patients will receive Therabands™ for resistance exercises and have access to a stationary bicycle for aerobic exercises with practical introduction by an exercise specialist. The partially supervised intervention is a progressive program with a goal of three aerobic and two resistance exercise sessions per week. Aerobic exercise will consist of 10-30 minutes of bicycling using a stationary bike (supervised or unsupervised) or brisk walking, following the Borg Scale of Rate of Perceived Exertion (RPE). Resistance exercise will include exercise for the upper and lower extremities with Therabands™. Exercise will be adapted based on the participant's clinical status for safety and ability to perform exercises. At the weekly supervised session, the exercise specialist will provide adequate progression of exercises, and review adherence to the intervention and provide support for questions and overcoming identified barriers to adherence. Participants assigned to the control group will receive our current standard of care. They will be reviewed by the ward physiotherapist on admission to hospital and encouraged to maintain physical activity by walking around the inpatient unit during their inpatient hospitalization. As per standard of care, the physiotherapist will be available on an as needed basis in both the inpatient and outpatient settings. Timely assessments of outcome measures outlined in the "Outcome Measures" section will be conducted for both groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hematological Malignancy
Keywords
Bone Marrow Transplantation, Exercise, Rehabilitation, Cancer

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Exercise Group
Arm Type
Experimental
Arm Description
Patients in the intervention group will receive supervised and unsupervised exercise program after their bone marrow transplant.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Patient will receive standard of care within the hospital as an inpatient and outpatient after their bone marrow transplant.
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Intervention Description
Combination of resistance and aerobic exercises for 100 days.
Primary Outcome Measure Information:
Title
Change in Quality of Life
Description
European Organization for Research and Treatment of Cancer Quality of Life Questionnaire. To investigate if a partially supervised exercise intervention in alloHSCT patients will result in differences in quality of life at Day 100 post transplant compared to the standard of care control group.
Time Frame
Baseline, Day 100 post-transplant
Secondary Outcome Measure Information:
Title
Changes in Quality of Life
Description
EuroQol (EQ)-5 Dimensions (5D) -3 Level (3L) Questionnaire.
Time Frame
Baseline, Hospital Discharge (approximately +30 days post-transplant), Day 60, 100, 365, and 730 post-transplant
Title
Changes in Grip Strength
Description
Using a handheld dynamometer, measured in kg.
Time Frame
Baseline, Hospital Discharge (approximately +30 days post-transplant), Day 60, 100, 365, and 730 post-transplant
Title
Changes in 30-Second Chair Stand
Description
Number of chair stands one can perform in 30 seconds.
Time Frame
Baseline, Hospital Discharge (approximately +30 days post-transplant), Day 60, 100, 365, and 730 post-transplant
Title
Changes in 6-Minute Walk Test
Description
Distance (meters) someone can walk in 6 minutes between two cones separated by 30 meters.
Time Frame
Baseline, Hospital Discharge (approximately +30 days post-transplant), Day 60, 100, 365, and 730 post-transplant
Title
Changes in Timed Up and Go
Description
Time taken for someone to stand up from a chair, walk 3 meters, turn around, walk back to the chair, and sit sound.
Time Frame
Baseline, Hospital Discharge (approximately +30 days post-transplant), Day 60, 100, 365, and 730 post-transplant
Title
Changes in Exercise Capacity
Description
Exercise Treadmill Test via Bruce or Modified Bruce Protocol. METs and estimated peak oxygen uptake (VO2) will be determined.
Time Frame
Baseline, Day 100, 365, and 730 post-transplant
Title
Changes in Cardiopulmonary Function
Description
Left ventricular ejection fraction vs radionuclide ventriculography (MUGA) or echocardiography.
Time Frame
Baseline, Day 100, 365, and 730 post-transplant
Title
Changes in Physical Activity Levels - Accelerometry
Description
Accelerometry counts converted minutes/week of moderate-to-vigorous activity and sedentary activity and METS. Godin Leisure-Time Exercise Questionnaire.
Time Frame
Baseline, Hospital Discharge (approximately +30 days post-transplant), Day 60, 100, 365, and 730 post-transplant
Title
Changes in Physical Activity Levels - Questionnaire
Description
Godin Leisure-Time Exercise Questionnaire. Total leisure activity score is calculated.
Time Frame
Baseline, Hospital Discharge (approximately +30 days post-transplant), Day 60, 100, 365, and 730 post-transplant
Title
Changes in Body Composition Analysis
Description
Height (cm), weight (m), and waist/hip circumference (cm) will be measured.
Time Frame
Baseline, Hospital Discharge (approximately +30 days post-transplant), Day 60, 100, 365, and 730 post-transplant
Title
Changes in Bone Mineral Density Analysis
Description
Bone mineral density testing will be performed using a Dual-Energy X-Ray Absorptiometry (DXA).
Time Frame
Baseline, Day 100, 365, and 730 post transplant
Title
Changes in Immune Biomarkers
Description
A collective blood test will be done to determine the composition of white blood cells (total, lymphocytes, and subsets of T-Lymphocytes).
Time Frame
Baseline, Day 100, 365, and 730 post-transplant

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients undergoing allogeneic stem cell transplantation (including related, unrelated, cord blood or haploidentical allogeneic transplant) for any indication through the Leukemia/BMT Program of British Columbia. Age greater than or equal to 18 years. Able to provide written informed consent. Exclusion Criteria: Severe cardiac disease including symptomatic congestive heart failure (New York Heart Association Class III or IV), unstable angina pectoris, or an unstable cardiac arrhythmia. Orthopedic illness which limits ability to conduct aerobic exercise (walking or biking). Not meeting eligibility criteria to proceed with allogeneic stem cell transplantation as per the Leukemia/BMT Program of BC.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stanley Hung, MSc
Phone
604-827-1914
Email
stanley.hung@ubc.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alina Gerrie, MD, FRCPC
Organizational Affiliation
British Columbia Cancer Agency
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Raewyn Broady, MBChB, FRCPC
Organizational Affiliation
British Columbia Cancer Agency
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vancouver General Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z1M9
Country
Canada
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alina Gerrie, MD
Phone
604-875-4863
Email
agerrie@bccancer.bc.ca

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Effects of Exercise on Allogeneic Stem Cell Transplant

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