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Clinical Trials/NCT07070388
NCT07070388CompletedNot Applicable

Robotic -Assisted Rehabilitation for Multiple Sclerosis: An Adaptive Approach for Individualized Therapy

Michael Holmes1 site in 1 country9 target enrollmentStarted: January 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
9
Locations
1
Primary Endpoint
Maximum isometric wrist force

Study Overview

Brief Summary

Therefore, the purpose of this study was to evaluate four-weeks of an upper limb robotic intervention for persons with Multiple Sclerosis. Participants completed a resistive and adaptive robotic training intervention whereby participants trained three times weekly for four consecutive weeks.

Detailed Description

Nine individuals with Multiple Sclerosis participated and were placed into two groups based that either trained their self-reported less affected limb (indirect training group; N=4) or trained their self-reported more affected limb (direct training group; N=5).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

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

Inclusion Criteria

  • •Diagnosis of MS
  • •No other neurological diagnosis
  • •No injury to the upper limb (i.e., broken bones)

Exclusion Criteria

  • •Relapse in the past 6 months

Arms & Interventions

Indirect training group

Experimental

trained their self-reported less affected upper limb

Intervention: end-effector robotic training (Device)

Direct training group

Experimental

trained their self-reported most affected limb

Intervention: end-effector robotic training (Device)

Outcomes

Primary Outcomes

Maximum isometric wrist force

Time Frame: Baseline (Week 0) and immediately post intervention (Week 4)

the participant's arm was fully extended and rested on the table, and participants were instructed to exert force at the wrist joint (F/E, RD/UD) as hard as they could against the stationary load cell that rested on the metacarpophalangeal joints (Model: BG 500, Mark-10 Corporation, New York, USA). Two maximal exertions were completed and the largest value was recorded.

maximum grip force

Time Frame: Baseline (Week 0) and immediately post intervention (Week 4)

Participants were asked to complete one trial of a maximum grip test (Baseline Evaluation Instruments). Held with a straight arm, 45° abduction by the side and hand/wrist neutral, participants were asked to squeeze the handle as hard as possible for 3 seconds and grip force (Newton) was recorded.

Maximum isometric wrist force

Time Frame: Baseline (Week 0) and immediately post intervention (Week 4)

the participant's arm was fully extended and rested on the table, and participants were instructed to exert force at the wrist joint (F/E, RD/UD) as hard as they could against the stationary load cell that rested on the metacarpophalangeal joints (Model: BG 500, Mark-10 Corporation, New York, USA). Two maximal exertions were completed and the largest value was recorded.

Secondary Outcomes

  • Wrist tracking task(Baseline (Week 0) and immediately post intervention (Week 4))
  • wrist range of motion(Baseline (Week 0) and immediately post intervention (Week 4))
  • Wolf Motor Function Test(Baseline (Week 0) and immediately post intervention (Week 4))
  • Wolf Motor Function Test(Baseline (Week 0) and immediately post intervention (Week 4))
  • Wrist tracking task(Baseline (Week 0) and immediately post intervention (Week 4))
  • wrist range of motion(Baseline (Week 0) and immediately post intervention (Week 4))

Investigators

Sponsor
Michael Holmes
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Michael Holmes

Associate Professor

Brock University

Study Sites (1)

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