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High Intensity Gait Training for Stroke (HIGT Trial)
N/A
Waitlist Available
Led By Patricia Broschart Valenza, DPT
Research Sponsored by Sunnyview Rehabilitation Hospital
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 (day 62 to day 86)-(day 14 to day 21)
Awards & highlights
No Placebo-Only Group
Summary
This trial tests if high intensity walking exercises during the initial phase of stroke recovery in rehab centers can improve walking, balance, and quality of life. It also checks if this approach is cost-effective and reduces healthcare needs after discharge.
Eligible Conditions
- Stroke
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ (day 62 to day 86)-(day 14 to day 21)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~(day 62 to day 86)-(day 14 to day 21)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
10 Meter Walk Test at Fast Speed
10 Meter Walk Test at Self Selected Speed
6 Minute Walk Test
+3 moreSecondary study objectives
5 Times Sit to Stand
Assistive Device Use
BERG Balance Scale
+1 moreAwards & 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: High Intensity Gait TrainingExperimental Treatment1 Intervention
HIGT will be performed 4-6 times per week in place of conventional physical therapy. The patient's heart rate(HR)and blood pressure(BP) will be measured throughout each session. If the HR or BP is out of the acceptable range, patients will undergo standard physical therapy for that session, and the medical team will be contacted.
Target HR zones will be calculated with the Karvonen formula. The first session goal is to reach a target HR range that is 50-60% of heart rate reserve. The goal for subsequent sessions is to reach 70-80% of heart rate reserve. Rate of perceived exertion (RPE) will also be utilized.
The primary therapist will design an individualized HIGT treatment program with a combination of speed dependent treadmill activities, activity-based treadmill activities, stair training, and over ground activities.
The patient will be reminded during each session to ask for a rest as needed. Standing rests are preferred over sitting rests, but either may be utilized.
Group II: ConventionalActive Control1 Intervention
The conventional physical therapy sessions are what a patient would normally receive during their rehabilitation. Physical therapy sessions are usually 60-90 minutes per day for 5 days each week, and possibly one 30-minute session on a 6th day. Physical therapy sessions are focused on gait, balance, and strengthening activities to address goals related to functional mobility. Clinicians administering therapy to patients in this arm will not be given instructions on the types of therapies they administer; however, they will not be permitted to do HIGT with patients. Therapists will be permitted to use other devices such as Ekso exoskeleton, Lite Gait, Rifton Tram Body Weight Support Devices, and Electrical Stimulation devices including the XCITE and RT300.
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Who is running the clinical trial?
Sunnyview Rehabilitation HospitalLead Sponsor
3 Previous Clinical Trials
342 Total Patients Enrolled
3 Trials studying Stroke
342 Patients Enrolled for Stroke
Patricia Broschart Valenza, DPTPrincipal InvestigatorSunnyview Rehabilitation Hospital
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are an adult who had a stroke resulting in weakness on one side of your body within the past three months.
Research Study Groups:
This trial has the following groups:- Group 1: Conventional
- Group 2: High Intensity Gait Training
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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