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Effect of an Exercise Rehabilitation Program on Symptoms in Hemodialysis

Primary Purpose

End-stage Renal Disease, Renal Failure Chronic Requiring Hemodialysis

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Exercise Rehabilitation
Sponsored by
University of Manitoba
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End-stage Renal Disease focused on measuring Hemodialysis, End-stage renal disease, Exercise, Symptom Burden

Eligibility Criteria

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

Inclusion Criteria:

  • greater than 3 months after starting chronic hemodialysis
  • no planned change in hemodialysis modality or relocation outside of Winnipeg during study intervention period (26 weeks)
  • assessed to be safe and able to exercise by HD unit nephrologist
  • ability to communicate in English and provide informed written consent

Exclusion Criteria:

  • acute coronary syndrome in past 3 months
  • unstable arrhythmia
  • shortness of breath at rest or with minimal activity (NYHA Class 4)
  • symptomatic hypoglycaemia (> 2x/week in week prior to enrolment)
  • currently participating in the Manitoba Renal Program clinical intradialytic cycling program
  • score of 0 on Dialysis Symptom Index when administered at time of consent

Sites / Locations

  • Health Sciences Centre
  • Seven Oaks General Hospital
  • St. Boniface Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Exercise Rehabilitation

Standard Care

Arm Description

Participants will receive baseline exercise counselling as per Standard Care group. Participants will then participate in a 26-week exercise rehabilitation program incorporating 3 components: One-to-one self-management/resistance education once per week during the first 4 weeks of intervention. Participants will subsequently receive resistance training material to allow for home exercise for the remaining 22 weeks of the intervention. Intradialytic aerobic exercise on a cycle ergometer 3 times weekly for 26 weeks at their usual hemodialysis sessions. Four additional one-to-one standardized education sessions will be completed during the intervention period.

Participants will receive one exercise counseling session as part of their baseline assessment. Participants in the control group will not undergo any other exercise counseling or formal exercise intervention, but will not be prohibited from participating in exercise outside of the study protocol.

Outcomes

Primary Outcome Measures

Change in dialysis symptom burden at 12 weeks
Measured using change in the Dialysis Symptom Index

Secondary Outcome Measures

Change in dialysis symptom burden at 26 and 52 weeks
Measured using change in the Dialysis Symptom Index
Change in modified symptom burden
Measured using change in modified Dialysis Symptom Index
Change in health-related quality of life
Measured by self-report using the EuroQol 5D-5L (EQ5D-5L) and EuroQol Visual Analogue Scale.
Change in time for recovery post-dialysis
Measured in minutes with the question "Approximately how much time does it take to recover from a dialysis session"
Change in endurance/exercise capacity
Measured using the Incremental Shuttle Walk Test
Change in frailty status
Measured using the Modified Fried Criteria for frailty.
Change in self-efficacy for exercise
Measured using the Self-Efficacy for Exercise Survey a 9 item self-reported assessment tool

Full Information

First Posted
October 3, 2014
Last Updated
August 2, 2023
Sponsor
University of Manitoba
Collaborators
The Wellness Institute at Seven Oaks General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02259413
Brief Title
Effect of an Exercise Rehabilitation Program on Symptoms in Hemodialysis
Official Title
Effect of an Exercise Rehabilitation Program on Symptom Burden and Quality of Life in Hemodialysis: A Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
May 2015 (Actual)
Primary Completion Date
June 8, 2023 (Actual)
Study Completion Date
June 8, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Manitoba
Collaborators
The Wellness Institute at Seven Oaks General Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether participation in a 26-week exercise rehabilitation program is effective at reducing symptom burden and improving quality of life in individuals receiving chronic hemodialysis.
Detailed Description
Individuals with end-stage kidney disease requiring HD suffer from multiple symptoms, which have limited effective treatments. Symptom burden, the combined impact of number and severity of symptoms, negatively impacts functional status and health-related quality of life (HRQOL) in HD. Small interventional trials suggest exercise can mitigate specific individual symptoms, but impact of exercise on overall symptom burden in HD is unknown. Dialysis patients have identified improving symptom burden and HRQOL as research priorities. We propose the first randomized controlled trial (RCT) investigating the effect of exercise rehabilitation on symptom burden in individuals on HD. Hypothesis: In individuals on HD, participation in a 26-week exercise rehabilitation (rehab) program will reduce symptom burden and improve HRQOL, resulting in reduced disability and improved long-term clinical outcomes as compared with standard care. Study Design: Single-centre RCT with one-to-one parallel design, allocation concealment and assessor blinding Study Population: Adults receiving chronic in-centre HD for > 3 months with at least one dialysis-related symptom; n=150 Intervention: Standard care plus 26-week structured rehab program (lifestyle education, resistance exercise and cycling during HD). Control: Standard care (baseline exercise counseling) Outcomes measured at baseline, 12, 26 and 52 weeks. Data Analysis: Will be performed on an intention to treat, available case basis with t-tests or Mann Whitney U for continuous outcomes, as per data distribution and Chi square tests for categorical outcomes. Mixed effects modeling will account for repeated outcome measures over time. Poisson regression will be performed for hospitalization analysis. Anticipated Outcomes: Mean symptom burden severity score will decrease by 20% from baseline in the intervention group at 12 weeks. Due to sustained physical activity in the intervention group, symptom burden will remain lower in this group at 6 months. In contrast, the control group will see no improvement in symptom burden from baseline.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End-stage Renal Disease, Renal Failure Chronic Requiring Hemodialysis
Keywords
Hemodialysis, End-stage renal disease, Exercise, Symptom Burden

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
172 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise Rehabilitation
Arm Type
Experimental
Arm Description
Participants will receive baseline exercise counselling as per Standard Care group. Participants will then participate in a 26-week exercise rehabilitation program incorporating 3 components: One-to-one self-management/resistance education once per week during the first 4 weeks of intervention. Participants will subsequently receive resistance training material to allow for home exercise for the remaining 22 weeks of the intervention. Intradialytic aerobic exercise on a cycle ergometer 3 times weekly for 26 weeks at their usual hemodialysis sessions. Four additional one-to-one standardized education sessions will be completed during the intervention period.
Arm Title
Standard Care
Arm Type
No Intervention
Arm Description
Participants will receive one exercise counseling session as part of their baseline assessment. Participants in the control group will not undergo any other exercise counseling or formal exercise intervention, but will not be prohibited from participating in exercise outside of the study protocol.
Intervention Type
Behavioral
Intervention Name(s)
Exercise Rehabilitation
Intervention Description
This intervention will consist of lifestyle education, home-based resistance exercise and stationary cycling during hemodialysis sessions. Duration of the intervention will be 26 weeks
Primary Outcome Measure Information:
Title
Change in dialysis symptom burden at 12 weeks
Description
Measured using change in the Dialysis Symptom Index
Time Frame
Measured at study baseline and 12 weeks after study start
Secondary Outcome Measure Information:
Title
Change in dialysis symptom burden at 26 and 52 weeks
Description
Measured using change in the Dialysis Symptom Index
Time Frame
Measured at study baseline, 26 and 52 weeks after study start
Title
Change in modified symptom burden
Description
Measured using change in modified Dialysis Symptom Index
Time Frame
Measured at study baseline, 12, 26 and 52 weeks after study start
Title
Change in health-related quality of life
Description
Measured by self-report using the EuroQol 5D-5L (EQ5D-5L) and EuroQol Visual Analogue Scale.
Time Frame
Measured at study baseline, 12, 26 and 52 weeks after study start
Title
Change in time for recovery post-dialysis
Description
Measured in minutes with the question "Approximately how much time does it take to recover from a dialysis session"
Time Frame
Measured at study baseline, 12, 26 and 52 weeks after study start
Title
Change in endurance/exercise capacity
Description
Measured using the Incremental Shuttle Walk Test
Time Frame
Measured at study baseline, 12, 26 and 52 weeks after study start
Title
Change in frailty status
Description
Measured using the Modified Fried Criteria for frailty.
Time Frame
Measured at study baseline, 12, 26 and 52 weeks after study start
Title
Change in self-efficacy for exercise
Description
Measured using the Self-Efficacy for Exercise Survey a 9 item self-reported assessment tool
Time Frame
Measured at study baseline, 12, 26 and 52 weeks after study start
Other Pre-specified Outcome Measures:
Title
Change in physical activity behaviour pattern
Description
Measured in 2 ways: Subjectively using the self-reported Godin-Shephard Leisure Time Physical Activity Questionnaire Objectively using multi-directional accelerometers (Actical Physical Activity Monitors TM) which will be worn for 7 days at each measurement time point 2.
Time Frame
Measured at study baseline, 12, 26 and 52 weeks after study start
Title
Hospitalization rate
Description
Measured by number of hospitalizations and length of stay for each hospitalization
Time Frame
Measured at study baseline, 12, 26 and 52 weeks after study start
Title
Mortality
Description
Measured as the proportion of people who died during the first year on dialysis
Time Frame
Measured at 1 year after starting dialysis

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: greater than 3 months after starting chronic hemodialysis no planned change in hemodialysis modality or relocation outside of Winnipeg during study intervention period (26 weeks) assessed to be safe and able to exercise by HD unit nephrologist ability to communicate in English and provide informed written consent Exclusion Criteria: acute coronary syndrome in past 3 months unstable arrhythmia shortness of breath at rest or with minimal activity (NYHA Class 4) symptomatic hypoglycaemia (> 2x/week in week prior to enrolment) currently participating in the Manitoba Renal Program clinical intradialytic cycling program score of 0 on Dialysis Symptom Index when administered at time of consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Clara J Bohm, MD, MPH
Organizational Affiliation
University of Manitoba
Official's Role
Principal Investigator
Facility Information:
Facility Name
Health Sciences Centre
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3A1R9
Country
Canada
Facility Name
Seven Oaks General Hospital
City
Winnipeg
State/Province
Manitoba
Country
Canada
Facility Name
St. Boniface Hospital
City
Winnipeg
State/Province
Manitoba
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

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Effect of an Exercise Rehabilitation Program on Symptoms in Hemodialysis

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