Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
All Genders
ID06965894

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

Age: 50Years - 80Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

Loading map...

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

Similar Trials

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here