12 Participants NeededMy employer runs this trial

Self-Supervised Movement Therapy for Stroke Recovery

PM
LW
Overseen ByLauren Wengerd
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Ohio State University
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

The goal of this clinical trial is to learn how a partially self-supervised constraint-induced movement therapy (sCIMT) program in adults with arm and hand weakness will work after stroke. This study will look at whether the program can help people improve the use of their arm and hand after a stroke while requiring less time with a therapist. The main questions it aims to answer are:

* Does the sCIMT program help people use their affected arm and hand better - after a stroke?

* Do participants feel that the sCIMT program is useful, easy to follow, and a good fit for their recovery needs?

* Does taking part in the sCIMT program improve participants' quality of life and daily well-being?

Participants will:

* Take part in a therapy program 5x/week for 2 weeks. The program is designed to help improve the use of the arm and hand affected by stroke.

* Wear a mitt on the stronger hand during certain practice activities to encourage use of the weaker hand.

* Complete surveys and tests before and after the program to measure arm and hand use, experiences with the program, and quality of life.

Are You a Good Fit for This Trial?

This trial is for adults aged 18–85 who had their first stroke at least two weeks ago and have moderate weakness in one arm or hand. Participants must be able to follow simple instructions, have enough movement in the unaffected arm, and not have other major health issues affecting participation.

Inclusion Criteria

I had my first stroke at least two weeks ago.
I am between 18 and 85 years old.
I use my weaker arm or hand very little in daily activities.
See 4 more

Exclusion Criteria

Comorbid diagnosis in addition to stroke (e.g., dementia, peripheral neuropathy) that could impact study results per investigator opinion
I have severe pain (6 or higher out of 10) in my shoulder, arm, or hand.
I am getting occupational therapy for my weak arm during the two-week study period.
See 5 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants take part in a self-supervised constraint-induced movement therapy (sCIMT) program 5 times a week for 2 weeks, designed to improve the use of the arm and hand affected by stroke.

2 weeks
10 sessions (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment, including assessments of upper extremity function and quality of life.

1 week
1 visit (in-person)

What Are the Treatments Tested in This Trial?

Interventions

  • Self-Supervised Constraint-Induced Movement Therapy (sCIMT)

Trial Overview

The study tests a self-supervised constraint-induced movement therapy (sCIMT) program where participants wear a mitt on their stronger hand to encourage use of the weaker one after stroke. The program runs five times per week for two weeks with less therapist supervision than usual.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Self-Supervised Constraint-Induced Movement TherapyExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Ohio State University

Lead Sponsor

Trials
891
Recruited
2,659,000+