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Exoskeleton-Assisted Rehabilitation for Stroke
N/A
Recruiting
Led By Michael Davidson, MSE MPH
Research Sponsored by Loma Linda University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up pre and post tests up to six weeks apart
Awards & highlights
No Placebo-Only Group
Summary
This trial will test if powered exoskeleton therapy can help improve quality of life for stroke patients as part of their rehabilitation program.
Who is the study for?
This trial is for adults over 18 who've had a stroke, can follow simple commands, and are within certain height and weight limits. They should have near-normal joint movement in legs and be part of a standing program. People who've already tried exoskeleton therapy can't join.
What is being tested?
The study compares three types of stroke rehabilitation: standard physical therapy, using a powered exoskeleton, or a mix of both. It aims to see if including the exoskeleton in treatment could become common practice for better recovery.
What are the potential side effects?
Potential side effects may include muscle soreness, fatigue from physical exertion during therapy sessions, skin irritation from the exoskeleton device, or discomfort due to unfamiliarity with the equipment.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ pre and post tests up to six weeks apart
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre and post tests up to six weeks apart
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
6 minute walk test
Berg Balance Test
Ten meter walk test
+2 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
3Treatment groups
Experimental Treatment
Group I: Group C - Physical Therapy onlyExperimental Treatment1 Intervention
Group C (n=12) will receive 18 visits of physical therapy, three times a week for approximately 6 weeks. Upon completion of the data collection portion of the study, group C will receive 9 sessions, three times a week for approximately three weeks of powered exoskeleton therapy. Data will not be collected or reported during this phase, but but may be retained for future approved use.
Group II: Group B - Powered Exoskeleton onlyExperimental Treatment1 Intervention
Group B (n=12) will receive 18 visits of powered exoskeleton only, three times a week for approximately 6 weeks.
Group III: Group A - Hybrid combinationExperimental Treatment1 Intervention
Group A (n=12) will receive 18 alternating visits of conventional physical therapy and powered exoskeleton gait training with a wearable robotic powered exoskeleton , three times a week for approximately 6 weeks.
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Who is running the clinical trial?
Loma Linda UniversityLead Sponsor
315 Previous Clinical Trials
266,554 Total Patients Enrolled
4 Trials studying Stroke
88 Patients Enrolled for Stroke
Michael Davidson, MSE MPHPrincipal Investigator - Loma Linda University O&P
Loma Linda University
1 Previous Clinical Trials
7 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You can move your knees, hips, and ankles almost like most people can.You have already used a powered exoskeleton for therapy.Adults who have had a stroke and are 18 years old or older.You have a score of 3 on the Ashworth scale when standing.You weigh less than 220 pounds and are between 5 feet and 6 feet 4 inches tall.
Research Study Groups:
This trial has the following groups:- Group 1: Group A - Hybrid combination
- Group 2: Group B - Powered Exoskeleton only
- Group 3: Group C - Physical Therapy only
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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