search
Back to results

A Comparison of Conventional Physical Therapy, Powered Exoskeleton, and Hybrid Physical Therapy With Exoskeleton

Primary Purpose

Stroke

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Hybrid combination of physical therapy and powered exoskeleton
Powered Exoskeleton Only
Physical Therapy only
Sponsored by
Loma Linda University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Stroke, Exoskeleton, Gait, Physical Therapy, Motor-learning

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Males and Females 18 years of age or older post-stroke

    • 3 Ashworth score are involved in a standing program less than 220 lbs 5'0" through 6'4" have the ability to follow one-step commands near normal range-of-motion for the knees, hips, and ankles

Exclusion Criteria:

  • Exclusion criteria will include those who have already experienced powered exoskeleton therapy.

Sites / Locations

  • Loma Linda UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Group A - Hybrid combination

Group B - Powered Exoskeleton only

Group C - Physical Therapy only

Arm Description

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.

Group B (n=12) will receive 18 visits of powered exoskeleton only, three times a week for approximately 6 weeks.

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.

Outcomes

Primary Outcome Measures

Timed up and go test
Subject sits in a standard armchair and stands, and at a self-selected walking speed, walks 3 meters, turns, and walks back to the chair, and sits down. They will be timed. Takes three minutes to administer.
Ten meter walk test
Subjects will be timed as they walk a known distance of 10 meters to determine his self-selected walking velocity (distance/time). They will be timed. Takes five minutes to administer.
6 minute walk test
This test measures distance walked in six minutes to assess a patient's physical endurance. They walk at a self-selected speed and will be timed. This test takes approximately 10 minutes to administer
Berg Balance Test
The Berg balance test is a reliable measure for predicting risk for fall. This 14-item test measures static and dynamic balance measures and takes 15-20 minutes to administer
The Activities-specific Balance Confidence (ABC) Scale
This has been shown to be an effective tool for assessing the psychological impact of balance impairment and falls and measuring an individual's balance confidence. Using a Likert scale, this self-administered test evaluates a person's confidence in balance over various activities. This 16-question test takes 5 to 10 minutes to complete.

Secondary Outcome Measures

Full Information

First Posted
November 24, 2020
Last Updated
February 27, 2023
Sponsor
Loma Linda University
search

1. Study Identification

Unique Protocol Identification Number
NCT04648878
Brief Title
A Comparison of Conventional Physical Therapy, Powered Exoskeleton, and Hybrid Physical Therapy With Exoskeleton
Official Title
A Comparison of Conventional Physical Therapy, Powered Exoskeleton, and Hybrid Physical Therapy With Exoskeleton in the Treatment of Individuals With Sub-acute and Chronic Stroke.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 14, 2021 (Actual)
Primary Completion Date
December 30, 2023 (Anticipated)
Study Completion Date
December 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Loma Linda University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this investigator-initiated study is to establish if powered exoskeleton therapy as a part of a rehabilitation program can be used as a standard of care in stroke rehabilitation.
Detailed Description
This prospective randomized control trial with three treatment arms will begin by: Determining if the subject is a candidate for exoskeleton treatment. Randomly assigning subjects to three groups (physical therapy only, exoskeleton only, or a hybrid of physical therapy and exoskeleton). Body measurements to individualize the fit of the exoskeleton to each subject at each session. Activities-based balance confidence (ABC) questionnaire will be administered before and after the study begins. Timed up and go test (TUGT). Ten-meter walk test (10MWT). Six-minute walk test (6MWT) Berg Balance Test (BBT). Five times sit to stand (5XSTS). Heart rate through a portable heartrate monitor.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Stroke, Exoskeleton, Gait, Physical Therapy, Motor-learning

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Care Provider
Masking Description
participants will be instructed to not reveal which treatment arm they have been assigned to
Allocation
Randomized
Enrollment
36 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A - Hybrid combination
Arm Type
Experimental
Arm Description
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.
Arm Title
Group B - Powered Exoskeleton only
Arm Type
Experimental
Arm Description
Group B (n=12) will receive 18 visits of powered exoskeleton only, three times a week for approximately 6 weeks.
Arm Title
Group C - Physical Therapy only
Arm Type
Experimental
Arm Description
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.
Intervention Type
Other
Intervention Name(s)
Hybrid combination of physical therapy and powered exoskeleton
Intervention Description
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
Intervention Type
Other
Intervention Name(s)
Powered Exoskeleton Only
Intervention Description
18 visits of powered exoskelton only, three times a week for approximately 6 weeks
Intervention Type
Other
Intervention Name(s)
Physical Therapy only
Intervention Description
18 visits of physical therapy only, three times a week for approximately 6 weeks
Primary Outcome Measure Information:
Title
Timed up and go test
Description
Subject sits in a standard armchair and stands, and at a self-selected walking speed, walks 3 meters, turns, and walks back to the chair, and sits down. They will be timed. Takes three minutes to administer.
Time Frame
Pre and post tests up to six weeks apart
Title
Ten meter walk test
Description
Subjects will be timed as they walk a known distance of 10 meters to determine his self-selected walking velocity (distance/time). They will be timed. Takes five minutes to administer.
Time Frame
Pre and post tests up to six weeks apart
Title
6 minute walk test
Description
This test measures distance walked in six minutes to assess a patient's physical endurance. They walk at a self-selected speed and will be timed. This test takes approximately 10 minutes to administer
Time Frame
Pre and post tests up to six weeks apart
Title
Berg Balance Test
Description
The Berg balance test is a reliable measure for predicting risk for fall. This 14-item test measures static and dynamic balance measures and takes 15-20 minutes to administer
Time Frame
Pre and post tests up to six weeks apart
Title
The Activities-specific Balance Confidence (ABC) Scale
Description
This has been shown to be an effective tool for assessing the psychological impact of balance impairment and falls and measuring an individual's balance confidence. Using a Likert scale, this self-administered test evaluates a person's confidence in balance over various activities. This 16-question test takes 5 to 10 minutes to complete.
Time Frame
Pre and post tests up to six weeks apart

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males and Females 18 years of age or older post-stroke 3 Ashworth score are involved in a standing program less than 220 lbs 5'0" through 6'4" have the ability to follow one-step commands near normal range-of-motion for the knees, hips, and ankles Exclusion Criteria: Exclusion criteria will include those who have already experienced powered exoskeleton therapy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michael Davidson, MSE MPH
Phone
9095586516
Email
mdavidson@llu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Davidson, MSE MPH
Organizational Affiliation
Loma Linda University O&P
Official's Role
Principal Investigator
Facility Information:
Facility Name
Loma Linda University
City
Loma Linda
State/Province
California
ZIP/Postal Code
92354
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michael J Davidson, MSE MPH
Phone
909-558-6516
Email
mdavidson@llu.edu

12. IPD Sharing Statement

Learn more about this trial

A Comparison of Conventional Physical Therapy, Powered Exoskeleton, and Hybrid Physical Therapy With Exoskeleton

We'll reach out to this number within 24 hrs