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Promoting Recovery Outcomes Through Precise Early Locomotor Interventions in Persons With Spinal Cord Injury

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06176833
Acronym
PROPEL-SCI
Enrollment
108
Registered
2023-12-20
Start date
2024-03-21
Completion date
2028-12-01
Last updated
2026-02-23

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

Conditions

Spinal Cord Injuries

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.

Interventions

For these training sessions, participants will undergo walking training sessions that consist of wearing a harness for either body weight support or as a safety precaution while walking on a treadmill.

Sponsors

Milap Sandhu
Lead SponsorOTHER
Baylor Scott and White Health
CollaboratorOTHER
University of Florida
CollaboratorOTHER

Study design

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

Intervention model description

Participants will be randomized into one of 4 intervention groups, based around if and when additional walking training is given following injury

Eligibility

Sex/Gender
ALL
Age
16 Years to 75 Years
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

Design outcomes

Primary

MeasureTime frameDescription
10 Meter walk test1-5 days Following InterventionUsed to assess walking speed, time taken to walk 10 meters at fastest pace

Secondary

MeasureTime frameDescription
6 Minute Walk test1-5 days Following InterventionUsed to assess distance traveled during a 6 minute walking test at a self selected pace
Walking Index for spinal cord injury1-5 days following interventionAssessment to determine the physical assistance and assistive devices needed to walk 10 meters
Daily step counts2 weeks following 3-, 6-, 9-, and 12- month assessmentsStep counts from a waist worn activity tracker
Gait Deviation idexBaseline, 3-, 6-, 9-, and 12- month assessmentsA measure of gait quality by quantifying joint angles during a gait cycle. This data is recorded via a marker-less motion capture system

Countries

United States

Contacts

CONTACTAlexander Barry, MS, CCRC
abarry@sralab.org3122381435
PRINCIPAL_INVESTIGATORMilap Sandhu, PhD

Shirley Ryan AbilityLab

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026