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Exercise for Improved Walking After Stroke
N/A
Recruiting
Led By Darcy Reisman, PhD
Research Sponsored by University of Delaware
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age 18-85
Able to walk at self-selected speed without assistance from another person
Must not have
Inability to walk outside the home prior to the stroke
Coronary artery bypass graft or myocardial infarction within past 3 months
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 hours
Awards & highlights
No Placebo-Only Group
Summary
This trial will test if a new walking pattern can be learned by stroke patients through distorted visual feedback, and if this pattern can be retained without visual feedback immediately after learning and 24 hours later. Subjects will be randomly assigned to the control group or the exercise group. The control group will simply complete the learning task, while the exercise group will complete 5 minutes of exercise immediately following the first retention test.
Who is the study for?
This trial is for individuals aged 18-85 who have had a single, unilateral stroke more than 6 months ago and can walk unassisted. They must have a specific level of stroke severity, confirmed by MRI or CT scan, and normal heart rate and blood pressure. People with recent serious heart issues, walking-limiting pain, additional neurological conditions, or severe communication problems cannot join.
What is being tested?
The study examines how exercise affects the ability to retain a new walking pattern learned through visual feedback in chronic stroke survivors. Participants are divided into two groups: one does the learning task only (control), while the other performs exercises after learning to see if it helps memory retention after 24 hours.
What are the potential side effects?
Since this trial involves exercise as an intervention post-stroke rehabilitation therapy, potential side effects may include muscle soreness or fatigue due to physical activity. However, no significant adverse effects are expected from the described interventions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am between 18 and 85 years old.
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I can walk on my own without help from others.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I couldn't walk outside my home before having a stroke.
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I have not had a heart bypass or heart attack in the last 3 months.
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I have pain in my muscles or bones that makes it hard to walk.
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I have had a stroke in the cerebellum, confirmed by MRI or CT scan.
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I have experienced unexplained dizziness in the past 6 months.
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I have a neurological condition besides stroke.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 hours
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
24 hour retention
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: ExerciseExperimental Treatment1 Intervention
Subjects will complete learning of a new walking pattern through distorted visual feedback and retention will be tested immediately without visual feedback. This will be followed immediately by 5 minutes of high intensity exercise. Retention without visual feedback will them be tested again 24 hours later.
Group II: ControlActive Control1 Intervention
Subjects will complete learning of a new walking pattern through distorted visual feedback and retention will be tested immediately after and 24 hours later (without visual feedback).
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Exercise
2016
Completed Phase 1
~820
Find a Location
Who is running the clinical trial?
University of DelawareLead Sponsor
161 Previous Clinical Trials
25,562 Total Patients Enrolled
12 Trials studying Stroke
4,393 Patients Enrolled for Stroke
Darcy Reisman, PhDPrincipal InvestigatorUniversity of Delaware
Media Library
Research Study Groups:
This trial has the following groups:- Group 1: Control
- Group 2: Exercise
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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