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Understanding Changes in Heart Function After Exercise in People With Stroke

University of British Columbia logo

University of British Columbia

Status

Completed

Conditions

Stroke

Treatments

Behavioral: Non-aerobic Exercise Program
Behavioral: Aerobic Exercise Program

Study type

Interventional

Funder types

Other

Identifiers

NCT01189045
H10-00735

Details and patient eligibility

About

Little is known about how exercise can affect heart function in stroke survivors.

This study will look at changes in cardiovascular fitness and function after 6 months of exercise. Volunteers will be tested before and after the program and again 2 months later to measure the effects on stroke risk factors, fitness level and flexibility of the arteries. Blood tests will measure cholesterol levels and other signs of inflammation.

This study will help us better understand how exercise after stroke can improve heart function and heart health, and ultimately help in lowering future stroke risk.

Full description

Purpose

To determine the effects of aerobic exercise after stroke on cardiorespiratory fitness, cardiovascular function, stroke risk factors, walking and health-related quality of life. This study will also examine the retention of these effects after the exercise program ends.

Methods

A randomized controlled study design will be used. Sixty participants will be randomized to participate in one of 2 treatment arms (6 months duration, 3 days / week, 1 hour / session):

  1. BALANCE AND FLEXIBILITY (non-aerobic) PROGRAM will be comprised of individualized upper and lower body stretching, or balance activities, yoga- or Tai Chi-style classes.
  2. AEROBIC PROGRAM will be comprised of a structured, progressive aerobic training program.

Participants will be evaluated at 3 time points - baseline (0 months), post-intervention (6 months) and follow up (8 months) - for stroke risk factors, cardiorespiratory fitness, arterial stiffness, echocardiography measures, inflammatory biomarkers, ambulatory capacity and health-related quality of life.

Enrollment

60 patients

Sex

All

Ages

50 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 50-80 years old
  • Has experienced a stroke
  • At least 12 months post-stroke
  • Able to stand independently
  • Able to walk at least 5 metres (assisted devices and guarded supervision is permitted)

Exclusion criteria

  • Stroke of non-cardiogenic origin (aneurysm, tumour)
  • Actively engaged in other stroke rehabilitation services
  • Class C or D American Heart Association Risk Criteria (uncontrolled arrhythmias)
  • Resting blood pressure > 160/100 mmHg
  • Significant musculoskeletal problems (rheumatoid arthritis) or other neurological conditions (e.g. Parkinson's)
  • Has a pacemaker
  • Pain or other co-morbidities (e.g. unclipped aneurysms, uncontrolled seizures etc.) which would preclude participation
  • Behavioural issues that would limit participation in exercise

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Aerobic Program
Experimental group
Description:
The Aerobic Program will be the Experimental arm of this trial, where a structured, progressive aerobic exercise will be conducted in a class format
Treatment:
Behavioral: Aerobic Exercise Program
Balance and Flexibility Program
Active Comparator group
Description:
The Balance and Flexibility Program will be a non-aerobic intervention that will act as an Active Comparator. Stretching, balance exercises, yoga- or Tai Chi-style classes will be conducted.
Treatment:
Behavioral: Non-aerobic Exercise Program

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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