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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05196204
Other study ID # CRIR-1497-1020
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 11, 2021
Est. completion date October 2022

Study information

Verified date January 2022
Source Centre for Interdisciplinary Research in Rehabilitation of Greater Montreal
Contact Dorothy Barthélemy, PhD, PT
Phone 514-343-7712
Email dorothy.barthelemy@umontreal.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objectives of the study are to evaluate trunk task-oriented training combined with function electrical stimulation (FES/T-TOT) efficacy on sitting balance and functional independence, and to understand the mechanisms of neuroplasticity that would improve functional independence following FES/T-TOT in individuals with spinal cord injury.


Description:

After obtaining their consent, participants will undertake evaluations at different times: 1. Assessment 3 weeks prior to training 2. Assessment 1 week prior to training 3. Training over 12 weeks 4. Assessment 1 week after training 5. Assessment 1 month after training (follow-up) Each assessment will be divided in 2 sessions and data will be collected over 2 days, at one session per day. The assessment will consist of: - Session 1 (at Neuro-Concept clinic) will include presentation of the study and the obtention of written consent, clinical (modified Reaching test and muscle strength), quality of life and functional independence assessments. - Session 2 (at IURDPM in Dr. Barthélemy's laboratory) will include postural control, corticospinal and cortical assessments. After the initial assessment, the participants with spinal cord injury will realize 36 sessions of trunk task-oriented training alone or combined with function electrical stimulation (3 times a week for 12 weeks).


Recruitment information / eligibility

Status Recruiting
Enrollment 45
Est. completion date October 2022
Est. primary completion date October 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility FOR PARTICIPANTS WITH SPINAL CORD INJURY Inclusion Criteria: - Level of spinal cord lesion between C6/C7 and T10 - At least, 6 months post-injury - Be considered as AIS A, B, C or D - Be able to sit without support for 15 seconds - Be able to provide informed consent in English or in French Exclusion Criteria: - To have cognitive deficits - To wear a corset - To have personal or family history of epilepsy - To have suffered moderate or severe traumatic brain injury - To have cochlear implant FOR CONTROL PARTICIPANTS Exclusion Criteria: - To have orthopedics problems - To have cognitive deficits - To have neurological problems

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Trunk-oriented task training combined with functional electrical stimulation
Training will consist to perform one hour of trunk task-oriented training combined with functional electrical stimulation (FES/T-TOT) specific for muscle strength and motor control. All training will be done seated without support with knees and hips flexed to 90 degrees. FES will be combined with functional and non-functional tasks to work functionality and muscle strengthening. Each training session will consist on the fulfilment of two functional tasks (as reaching) and two non-functional tasks (as push-up movement) from a battery of postural control exercises.
Trunk-oriented task training alone
The SCI participants who will perform T-TOT training alone will have to perform the same exercises as explained in the previous section (two functional tasks and two non-functional tasks) but they will not receive any functional electrical stimulation. Training will consist to perform one hour of trunk task-oriented training (T-TOT) specific for muscle strength and motor control. All training will be done seated without support with knees and hips flexed to 90 degrees. Each training session will consist on the fulfilment of two functional tasks (as reaching) and two non-functional tasks (as push-up movement) from a battery of postural control exercises.

Locations

Country Name City State
Canada Neuro-Concept Inc Montreal Quebec
Canada Neuromobility lab Montréal Quebec

Sponsors (3)

Lead Sponsor Collaborator
Centre for Interdisciplinary Research in Rehabilitation of Greater Montreal Mitacs, Neuro-Concept Inc.

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Physical Activity Recall Assessment for People with Spinal Cord Injury (questionnaire) This interview will capture all physical activity information over the previous 3 days. Eight periods of day will be screened (morning routine, breakfast, morning, lunch, afternoon, dinner, evening, evening routine). This test allows us to verify if the intensity of daily physical activity of each participant will be constant during the intervention. Before and after the 12-week trainings
Other Change in quality of life using World Health Organization Quality of Life with disabilities module (WHOQOL-BREF) This questionnaire consists in 39 questions about participant feelings. Before and after the 12-week trainings and 1-month follow-up
Other Change in quality of life using Short-Form 36 questionnaire The questionnaire consists in 36 questions about 8 domains: physical functioning, role functioning-physical, bodily pain, general health, vitality, social functioning, role functioning-emotional and mental health Before and after the 12-week trainings and 1-month follow-up
Other Change in the Quality of life index This questionnaire consists in 37 questions about 4 domains: health and functioning, psychological/spiritual, social and economic, and family. Before and after the 12-week trainings and 1-month follow-up
Other Change in functional independence using Spinal Cord Independence Measure questionnaire This questionnaire consists in evaluation of self-care, respiration and sphincter management, and a participant's mobility abilities. Before and after the 12-week trainings and 1-month follow-up
Primary Change in Function in Sitting Test This test evaluates the sitting balance via 14 everyday functional activities rated from 0 to 4 according to the reactions of the participants. Before and after the 12-week trainings and 1-month follow-up
Primary Change in modified Functional Reach Test This test evaluates the ability for each participant to realize a lateral and anterior trunk flexion in order to observe the maximum distance reached. Before and after the 12-week trainings and every 4-weeks during the training period
Secondary Change in EMG activation pattern of electromyographic activity of muscles in the trunk during reaching and pointing tasks Before and after the 12-week trainings and 1-month follow-up
Secondary Change in the center of pressure excursion during reaching and pointing tasks Before and after the 12-week trainings and 1-month follow-up
Secondary Modification of the excitability of the reticulospinal pathway using the acoustic startle response A tone will be triggered just before the reaching movement. The EMG responses of trunk muscles will be analyzed. Before and after the 12-week trainings and 1-month follow-up
Secondary Modification of the excitability of the vestibulospinal pathway using galvanic vestibular stimulation Vestibular responses induced by GVS will be identified in the trunk muscles Before and after the 12-week trainings and 1-month follow-up
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