Skip to content

Circuit Training Program for Persons With Spinal Cord Injury

Circuit Training Program Tom Improve Endocrine-Metabolic Function in Persons With Spinal Cord Injury

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04263272
Enrollment
16
Registered
2020-02-10
Start date
2020-02-29
Completion date
2020-07-31
Last updated
2020-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Cord Injuries

Keywords

Endocrine-Metabolic health, Cardio-Metabolic health

Brief summary

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.

Detailed 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).

Interventions

OTHERUpper Body Circuit Training Program

16 week seated upper body exercise for persons with Spinal Cord Injuries. Participants will attend 2-3 exercise sessions a week, sessions have a mix of SCI community members and inpatients.

Sponsors

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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)

Design outcomes

Primary

MeasureTime frameDescription
Feasibility surveyAfter Study Completion (16 weeks)Feasibility question options range from -3 to +3 on a likert scale, higher scores indicated a greater level of feasibility.
Injury Characteristics SurveyBaselineDate of injury (DD/MM/YYYY)
Change in Spinal Cord Injury Independence Measure - MobilityBaseline and 16 weeksAssessment of degree to which participant can independently preform mobility tasks, such as transfers, and the ue of mobility aids.
Change in Upper and Lower Extremity Strength by a manual muscle test (MMT)Baseline and 16 weeksAssessment of joint (Shoulder, elbow, wrist, hip, knee and ankle) muscle strength using a Manual muscle test.
Change in Upper and Lower Extremity Range of MotionBaseline and 16 weeksAssessment of joint range of motion in the upper and lower extremities (Shoulder, elbow, wrist, hip, knee and ankle)
Change in Spasticity in upper and lower extremities using the Modified Ashworth ScaleBaseline and 16 weeksAssessment of muscle tone through range of motion, on a scale of 0-4 (0= no increase in muscle tone; 4 = rigidity in flexion or extension)
Change in Maximal Safe Wheel chair speed measured using the Propulsion Speed TestBaseline and 16 weeks20 meter straight line wheel chair speed test. 3 trails were be preformed at a comfortable speed and 3 trials will be preformed at a maximal but safe speed.
Change in Ability to safety navigate wheel chair using the Slalmon Speed testBaseline and 16 weeksObjective is to weave between a set of cones without touching them as fast as safely possible. 3 attempts will be given.
Demographics and Lifestyle QuestionnairesBaselineAge in years
Change in MedicationsBaseline and 16 weeksList of medication and supplements currently being taken.
Change in Experienced PainBaseline and 16 weeksThe international Spinal Cord Injury Pain Data Set will be used to evaluate the presence and severity of pain. Description of 3 main pain concerns and there intensity. Intensity ranges from 0 = no pain to 10 = worst possible pain.
Change in Wheel Chair skills ability using the Wheel Chair skills Test QuestionnaireBaseline and 16 weeksQuestionnaire assesses the ability and confidence in preforming numerous wheel chair skills (ex: turning the wheelchair around a small space) Questions answers include 'No' 'partially' 'yes' 'very well'.
Change in Well Being measured by the General Wellbeing IndexBaseline and 16 weeksAssessment of emotional wellbeing, on a scale of 0-5.
Change in Quality of life and health measured by the WHOQOL-BREFBaseline and 16 weeksSelf reported questionnaire assessing quality of life (physical, social, environment and psychological health) on a scale of 1 - 4 (1=poor/not al all; 5= very good/extreme amount)
Change in aerobic capacity (VO2max) measured by 6-min wheelchair propulsion testBaseline and 16 weeksObjective is to get the largest total distance. Pylons are placed 25meters apart, participants starts in the middle go around the first cone to the let return to the middle and make a full stop, then continue to the right of second cone, go around it and back to the middle, making a figure 8. Continue that pattern for 6 minutes.
Blood TestBaseline and 16 weeksMeasurement of metabolic profile (ex: glucose, insulin, triglyceride)
Change in Body composition measured by DEXA (Dual energy x-ray absorptiometry)Baseline and 16 weeksMeasurement of bone mineral density of the full body (reported using a T score)

Contacts

Primary ContactDalton Wolfe, PhD
dwolfe@uwo.ca5196854292
Backup ContactStephanie Marrocco, MSc
stephanie.marrocco@sjhc.london.on.ca5196854292

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026