Clinical Trials Directory

Trials / Completed

CompletedNCT00786045

Fitness Intervention Trial for Stroke

Fitness Intervention Tiral for Stroke: Enhancing Walking Endurance Using Home Rehabilitation Programs

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
McGill University · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The objective of this study is to evaluate, among persons who have completed the restorative phase of stroke and have ceased rehabilitation, the relative effectiveness in improving functional exercise capacity of two programs for continued care, a home-based general fitness training program using stationary cycling and a disability targeted, home-based exercise program to enhance mobility and walking competency. capacity compared with the "walking" group and that consequently the cycle group will achieve a higher quality of life. A secondary objective is to explore factors associated with compliance with the exercise regimens. Previous research has indicated that cognitive-affective-behavioural profile is related to exercise activity in a number of populations including sedentary adults, older adults and patients with cardiovascular disease. As we anticipate that one of the mechanisms by which the cycling will result in an outcome better than the more traditional type of disability tailored exercise program is through greater compliance, this second objective is very relevant. This study will also address the impact of regular exercise on cardio-vascular risk factor profile.

Detailed description

The specific clinical hypothesis to be tested is that, over a one year period, persons assigned to the general fitness "cycle" group will experience a greater increase in functional exercise

Conditions

Interventions

TypeNameDescription
OTHERHome Cycling ProgramParticipants will be given a time and intensity graded program at an intensity that is comfortable and tolerable for the individual. The individual will be encouraged to augment, gradually, either the time of cycling per day or the work of cycling, always keeping within the limits of comfort and tolerability. Participants will also be given a target heart rate threshold to try and meet but not to exceed. This will be based their response to the stress test and will most likely be between 50% and 70% of maximum age-predicted heart rate. The aim is to build up to one-half hour of cycling per day. All bicycles will be equipped with electronic monitoring of speed, distance, and heart rate.

Timeline

Start date
2002-11-01
Primary completion
2009-11-01
Completion
2009-11-01
First posted
2008-11-05
Last updated
2013-04-29

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00786045. Inclusion in this directory is not an endorsement.