Actively Recruiting
Effect of Pressure Splints on Lower Extremity Functions in Hemiplegic Stroke Patients
Led by Istinye University · Updated on 2025-05-16
30
Participants Needed
1
Research Sites
2 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are exploring how pressure splints affect lower leg movement and function in people who have hemiplegia caused by stroke. Hemiplegia often weakens or paralyzes one side of the body, making it hard to walk or move the legs properly. This study aims to find better rehabilitation methods to improve recovery for stroke patients by supporting and enhancing muscle function with pressure splints. Participants will be randomly placed in one of two groups for six weeks. Both groups will receive neurodevelopmental therapy and proprioceptive neuromuscular facilitation (PNF) exercises. The experimental group will use a Johnston pressure splint on the affected lower leg during therapy, while the control group will do the exercises without the splint. This comparison will help evaluate the added impact of the pressure splint. During the study, participants will be assessed on lower extremity motor function, balance, strength, and mobility over about eight months. Researchers will also monitor stroke recovery, walking ability, independence, and muscle tone. The study includes safety and progress monitoring through regular evaluations during and after the intervention to understand the full effects of pressure splints on hemiplegic stroke rehabilitation.
CONDITIONS
Brief Title
Lower Extremity Pressure Splints in HP
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Having hemiplegia because of stroke
- Time since stroke: 1 month to 1 year
- Ability to participate (a score of >24 on the Mini-Mental State Examination)
- Being voluntary
- Age between 50-80
You will not qualify if you...
- Severe cognitive impairment
- Other neurological disorders
- Severe comorbidities or spasticity on lower extremity
- Contraindications to exercise
- Recurrent stroke
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 8 months
Participants receive a rehabilitation program including neurodevelopmental therapy and proprioceptive neuromuscular facilitation (PNF) techniques. Those in the splint group will have a Johnston pressure splint applied to the affected lower extremity during therapy sessions to support motor recovery, balance, and gait.
Regular therapy sessions during treatment period
Trial Site Locations
Total: 1 location
1
Monseigneur Cortbawi Hospital
Jounieh, Keserwan, Lebanon, 1200
Actively Recruiting
Research Team
Ç
Çiçek Günday, Asst. Prof.
O
Ousama Maarbani, Physiotherapist
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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