Actively Recruiting
Isokinetic Strength Training in Hemiparetic Patient With Knee Extension Thrust
Led by Rennes University Hospital · Updated on 2023-09-05
12
Participants Needed
1
Research Sites
171 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to assess the impact of an isokinetic strength training of knee flexor and extensor muscles on walking performance in hemiparetic patients with knee extension thrust.
CONDITIONS
Official Title
Isokinetic Strength Training in Hemiparetic Patient With Knee Extension Thrust
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Hemiparetic patient (hemorragic or ischemic stroke)
- Subacute stage (< 6 Months) or chronic stage of stroke (> 6 months) (6 patients in each group)
- Age between 18 and 75 years
- Able to walk 10 meters independently without any assistive devices
- Knee extension thrust during stance phase of gait cycle (rapid posterior movement of the knee toward extension)
- Scheduled rehabilitation program with isokinetic strength training
- Affiliation to a social security
- Patients who received and signed informed consent
You will not qualify if you...
- Major comprehension deficit that does not allow giving informed consent and participating in isokinetic strength training (assessed with comprehension subscore of Language screening Test)
- Unstable cardiovascular condition
- Musculoskeletal disorders with knee pain that do not allow isokinetic strength training
- Botulinum toxin injection less than 3 months ago or repeated injection in lower limb
- Proprioception trouble assessed with proprioception section of the Fugl-Meyer Assessment [FMA-P] 0/2
- Spasticity of triceps surae 62 (Modified Ashworth scale)
- Ankle dorsiflexion angle less than 90�b0
- Pregnant women or breastfeeding
- Persons with safety measures
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
CHU de Rennes
Rennes, France, 35033
Actively Recruiting
Research Team
S
Sophie HAMEAU, PhD
CONTACT
K
Krsitell COAT
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
FACTORIAL
Primary Purpose
TREATMENT
Number of Arms
3
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