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Clinical Trials/NCT06176833
NCT06176833RecruitingNot Applicable

Critical Time Window for Rehabilitation After Incomplete Spinal Cord Injury: Early vs Late Locomotor Training

Milap Sandhu2 sites in 1 country108 target enrollmentStarted: March 21, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
108
Locations
2
Primary Endpoint
10 Meter walk test

Study Overview

Brief Summary

The purpose of this study is to evaluate if a specific type of additional walking therapy, called body weight supported treadmill training (BWSTT) affects walking ability following a traumatic spinal cord injury. Specifically, the study will look at whether starting BWSTT, which uses a body harness to support body weight while walking on a treadmill at different times within the first 6 months after the injury, makes a difference in how effective this therapy may be, While we know that the brain re-learns patterns following an injury, there has not been a lot of prior research evaluating how starting this type of walking therapy at specific times within the first 6 months after injury may impact any effectiveness of the additional therapy.

The study will randomize participants into four groups: those who start this therapy within 60 days, within 3 months, within 6 months or who do not receive this additional research therapy. Randomization means that which group you will be in as part of this study is determined by chance, like the flip of a coin. The additional walking therapy for this research study, if you are randomized for one of the three groups who receives the additional therapy, will be given on top of (meaning in addition to) any standard of care therapies that you may be receiving at that time point after your injury.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Investigator, Outcomes Assessor)

Masking Description

Investigator and outcome assessor will have no knowledge of groups, cannot blind participants as they know when they will be receiving the additional training

Eligibility Criteria

Ages
16 Years to 75 Years (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • History of Acute and Traumatic SCI with AIS classification of B, C, or D between the neurological levels of C5 and T12
  • Between the ages of 16-74
  • Weight bearing as tolerated in bilateral lower extremities
  • Able to tolerate a harness
  • Ability to provide informed consent. For minors, consent of parents or primary caregivers/guardians and assent of the minor
  • Able to provide informed consent within 60 days of injury onset
  • Able to participate in all study related activities, including 1-year follow up

Exclusion Criteria

  • Orthopedic injuries, fractures, surgeries, or other conditions affecting locomotor function or weight bearing
  • A weight over 250lbs and if so a BMI greater than 30, or deemed clinically inappropriate due to body habitus
  • Moderate to sever traumatic brain injury of other neurological conditions at a severity which impairs cognition
  • Presence of uncontrolled orthostatic hypotension that limits active participation in intense physical rehabilitation program.
  • Other medical complications such as severe heart failure or large/deep pelvic or lower abdominal wounds that may limit the ability to safely don and doff a harness for ambulation
  • Pregnancy, as confirmed by blood draw

Arms & Interventions

Early Intervention

Active Comparator

Additional training will begin no more than 60 days following spinal cord injury

Intervention: Body Weight Supported Treadmill Training (Procedure)

Sub-acute Intervention

Active Comparator

Additional training will occur 3 months following spinal cord injury

Intervention: Body Weight Supported Treadmill Training (Procedure)

Chronic Intervention

Active Comparator

Additional training will occur 6-12 months following SCI

Intervention: Body Weight Supported Treadmill Training (Procedure)

Standard of Care

No Intervention

This group only receives standard of care treatment but is assessed at the same time points as the other groups

Outcomes

Primary Outcomes

10 Meter walk test

Time Frame: 1-5 days Following Intervention

Used to assess walking speed, time taken to walk 10 meters at fastest pace

Secondary Outcomes

  • 6 Minute Walk test(1-5 days Following Intervention)
  • Daily step counts(2 weeks following 3-, 6-, 9-, and 12- month assessments)
  • Gait Deviation idex(Baseline, 3-, 6-, 9-, and 12- month assessments)
  • Walking Index for spinal cord injury(1-5 days following intervention)

Investigators

Sponsor
Milap Sandhu
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Milap Sandhu

Principal Investigator

Shirley Ryan AbilityLab

Study Sites (2)

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