Losing Balance to Prevent Falls After Spinal Cord Injury (RBT+FES)
Primary Purpose
Spinal Cord Injuries
Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Reactive balance training
Sponsored by
About this trial
This is an interventional treatment trial for Spinal Cord Injuries focused on measuring balance training, falls
Eligibility Criteria
Inclusion Criteria:
- Participant sustained a traumatic motor iSCI (i.e. AIS C or D) at T12 or above.
- Injury occurred more than a year prior to study enrollment (when natural recovery has plateaued).8,9
- Participant is ≥18 years old.
- Participant can attend three training sessions/week for six weeks (i.e. has reliable transportation).
- Participant is able to stand for >30 seconds without upper limb support or assistance (i.e. scores 2/4 on item two of the Berg Balance Scale, Standing Unsupported10). This criterion ensures the participant will be able to participate in upright balance exercises.
- Participant requires physical assistance, a gait aid or a brace to ambulate 10 meters (i.e. self-selected score of 1-19 on the Walking Index for Spinal Cord Injury (WISCI) II).
Exclusion Criteria:
- Participant presents with contraindications to FES (i.e. implanted electronic device, radiation in past six months, active deep vein thrombosis, pregnancy).12
- Participant presents with other conditions besides iSCI that affect balance (e.g. vestibular disorder, brain injury).
- Participant has a pressure injury (>grade 2) on the pelvis or trunk where the safety harness will be applied, or on the foot where the foot switch will be applied.
- Participant has a history of a lower limb fragility fracture.
Sites / Locations
- KITE-Toronto Rehabilitation Institute, UHNRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Reactive balance training plus functional electrical stimulation
Reactive balance training
Arm Description
Outcomes
Primary Outcome Measures
Berg Balance Scale
mini-Balance Evaluation Systems Test
Activities-specific Balance Confidence Scale
Falls Efficacy Scale - International
Isometric strength
The isometric strength of eight lower extremity muscle groups (hip extensors, hip flexors, hip abductors, hip adductors, knee extensors, knee flexors, ankle plantarflexors, ankle dorsiflexors) will be tested bilaterally using hand-held dynamometry.
Proprioception of the ankle joints
To test proprioception, participants will assume a supine position with their eyes closed while the blinded assessor moves the ankle joint six times slowly through 10° of dorsiflexion (i.e. up) or plantarflexion (i.e. down). Participants will be asked to state the perceived direction of movement (i.e. up or down). This process will be repeated six times for each ankle, with a score of 1 assigned for each correct response. Each ankle will receive a maximum score of 6 for a total possible score of 12 (i.e. 2 joints x 6 trials/joint).
Lean-and-Release Test
A lab-based assessment of reactive stepping ability.
Tracking falls
Falls will be monitored for six months following the intervention
Secondary Outcome Measures
Full Information
NCT ID
NCT04881565
First Posted
May 5, 2021
Last Updated
November 1, 2022
Sponsor
University Health Network, Toronto
1. Study Identification
Unique Protocol Identification Number
NCT04881565
Brief Title
Losing Balance to Prevent Falls After Spinal Cord Injury (RBT+FES)
Official Title
Losing Balance to Prevent Falls After Spinal Cord Injury
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 27, 2021 (Actual)
Primary Completion Date
July 30, 2024 (Anticipated)
Study Completion Date
July 30, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Falls are a health crisis that cost health care systems billions of dollars/year. This crisis is especially relevant for individuals living with incomplete spinal cord injury (iSCI); 78% fall at least once annually. In able-bodied individuals, falls are prevented by taking reactive steps; however, these reactions are impaired after iSCI. Research in stroke and geriatric rehabilitation showed that reactive balance training (RBT), which targets reactive stepping, prevents falls. We developed a modified version of RBT for the iSCI population. RBT resulted in fewer falls post-training compared to dose-matched, conventional balance training. However, only those who were able to take a step independently and without upper limb support were able to participate in RBT, limiting the applicability of this promising fall prevention method. To address this limitation, we will integrate functional electrical stimulation into RBT (RBT+FES). Our study aims to provide a preliminary evaluation of the efficacy of RBT+FES in participants with chronic, motor iSCI. We will complete a pilot randomized clinical trial (RCT) with 22 participants with iSCI. Participants will be randomly allocated to RBT+FES or to RBT alone (i.e. without FES). They will complete 18 training sessions over 6 weeks (3 sessions/week). Clinical and biomechanical assessments of balance, strength and proprioception will be completed before training, immediately after training, and six months post-training. Falls will be monitored for six months after training through an online survey and regular phone calls. Performance on clinical and biomechanical measures and fall data will be compared between groups. This research will inform the need for, and design of, a larger RCT, and has the potential to transform fall prevention after iSCI.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injuries
Keywords
balance training, falls
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
The clinical measures of balance, strength and proprioception will be administered by a physical therapist blind to group allocation. The physical therapist will not work at the facility where the research is being conducted, therefore reducing the likelihood of a breach of allocation concealment. If a breach occurs, it will be reported in the final publication.
Allocation
Randomized
Enrollment
22 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Reactive balance training plus functional electrical stimulation
Arm Type
Experimental
Arm Title
Reactive balance training
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
Reactive balance training
Intervention Description
During each one-hour session, participants will experience 40-50 perturbations (i.e. approximately one perturbation per training minute) during standing and/or walking activities. The perturbations will be applied in any direction (e.g. forwards, sideways, backwards, etc.) To create a perturbation, the researcher will apply unexpected pushes or pulls to a safety harness at waist level. The perturbation will be sufficient in magnitude to elicit a stepping response from the participant. Throughout the session, participants will complete challenging balance tasks, customized to their ability level. Balance tasks will be organized into five categories: stable, quasi-mobile, mobile, unpredictable and participant-selected.
Primary Outcome Measure Information:
Title
Berg Balance Scale
Time Frame
Change from baseline to 6-month follow-up
Title
mini-Balance Evaluation Systems Test
Time Frame
Change from baseline to 6-month follow-up
Title
Activities-specific Balance Confidence Scale
Time Frame
Change from baseline to 6-month follow-up
Title
Falls Efficacy Scale - International
Time Frame
Change from baseline to 6-month follow-up
Title
Isometric strength
Description
The isometric strength of eight lower extremity muscle groups (hip extensors, hip flexors, hip abductors, hip adductors, knee extensors, knee flexors, ankle plantarflexors, ankle dorsiflexors) will be tested bilaterally using hand-held dynamometry.
Time Frame
Change from baseline to 6-month follow-up
Title
Proprioception of the ankle joints
Description
To test proprioception, participants will assume a supine position with their eyes closed while the blinded assessor moves the ankle joint six times slowly through 10° of dorsiflexion (i.e. up) or plantarflexion (i.e. down). Participants will be asked to state the perceived direction of movement (i.e. up or down). This process will be repeated six times for each ankle, with a score of 1 assigned for each correct response. Each ankle will receive a maximum score of 6 for a total possible score of 12 (i.e. 2 joints x 6 trials/joint).
Time Frame
Change from baseline to 6-month follow-up
Title
Lean-and-Release Test
Description
A lab-based assessment of reactive stepping ability.
Time Frame
Change from baseline to 6-month follow-up
Title
Tracking falls
Description
Falls will be monitored for six months following the intervention
Time Frame
Change from beginning to end of 6-month follow-up period
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Participant sustained a traumatic motor iSCI (i.e. AIS C or D) at T12 or above.
Injury occurred more than a year prior to study enrollment (when natural recovery has plateaued).8,9
Participant is ≥18 years old.
Participant can attend three training sessions/week for six weeks (i.e. has reliable transportation).
Participant is able to stand for >30 seconds without upper limb support or assistance (i.e. scores 2/4 on item two of the Berg Balance Scale, Standing Unsupported10). This criterion ensures the participant will be able to participate in upright balance exercises.
Participant requires physical assistance, a gait aid or a brace to ambulate 10 meters (i.e. self-selected score of 1-19 on the Walking Index for Spinal Cord Injury (WISCI) II).
Exclusion Criteria:
Participant presents with contraindications to FES (i.e. implanted electronic device, radiation in past six months, active deep vein thrombosis, pregnancy).12
Participant presents with other conditions besides iSCI that affect balance (e.g. vestibular disorder, brain injury).
Participant has a pressure injury (>grade 2) on the pelvis or trunk where the safety harness will be applied, or on the foot where the foot switch will be applied.
Participant has a history of a lower limb fragility fracture.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Principal Investigator, PhD
Phone
416-597-3422
Ext
6190
Email
kristin.musselman@uhn.ca
Facility Information:
Facility Name
KITE-Toronto Rehabilitation Institute, UHN
City
Toronto
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kristin Musselman
Email
kristin.musselman@uhn.ca
12. IPD Sharing Statement
Learn more about this trial
Losing Balance to Prevent Falls After Spinal Cord Injury (RBT+FES)
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