Circuit Training Program for Persons With Spinal Cord Injury

Lawson Health Research Institute

Status

Unknown

Conditions

Spinal Cord Injuries

Treatments

Other: Upper Body Circuit Training Program

Study type

Interventional

Funder types

Other

Identifiers

NCT04263272

113642

Details and patient eligibility

About

This initiative represents development and pilot testing of a circuit training exercise program for persons with spinal cord injury (SCI) to be implemented within a rehabilitation centre. The program will integrate members of the community who are > 18 months post-injury with those currently participating in SCI rehabilitation as inpatient.

Full description

This initiative represents development and pilot testing of a 16 week circuit training exercise program for persons with spinal cord injury (SCI) to be implemented within a rehabilitation centre (Parkwood Institute, London, ON). The primary purpose of this trial is one of feasibility - i.e., testing out several aspects of the trial for the purposes of determining what features of the exercise intervention and the various outcome measurements might be a part of subsequent trials. In addition, a subset of this data will serve as preliminary comparison information for Dr. Dany Gagnon's study at the University of Montreal. In this way, this is not a true multi-centre trial in that we are not conducting an identical protocol to a study he is conducting. Rather, we are using some of the same outcome measures and an exercise intervention that has some similar parameters to one that he is implementing in Montreal - with a view to providing a preliminary comparison of outcomes of a subset of participants in our study so as to inform the development of future studies. For this reason, the group of community-dwelling persons with SCI will have more cardio-metabolic outcome measurements taken, as they represent the primary group of interest to Dr. Gagnon.

Overall, the program will integrate members of the community who are > 18 months post-injury (n=8) with those currently participating in SCI rehabilitation as inpatients (n=8). Outcomes will be collected to test the effects of the program on an array of cardio-metabolic measures in those participants with chronic SCI, as well as the feasibility of the program for all participants (N=16). Note: although a participant can decline to continue participation at any time, it is likely that many inpatient participants will choose to not continue participation if this proves logistically difficult (if they move back to their home community away from London).

Enrollment

16 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Community:

Chronic traumatic or non-traumatic SCI between level C6 and T10 >18 months post injury
manual wheelchair as the primary mode of mobility
no existing conditions that would make it unsafe to participate in an exercise program (e.g., fractures).
Ability to understand and communicate in English.
18 years or older.

Inpatients:

Chronic traumatic or non-traumatic SCI between level C6 and T10
manual wheelchair as primary mode of mobility
no existing conditions that would make it unsafe to participate in an exercise program (e.g., fractures).
Ability to understand and communicate in English.
18 years or older.

Exclusion criteria

Power wheelchair users (Non manual wheelchairs)
Have an existing condition that would make it unsafe to participate in an exercise program (e.g., fracture)