Actively Recruiting
Effects of Robotic Glove Hand Training in Patients After Median Nerve Transfer
Led by Riphah International University · Updated on 2024-06-26
46
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Selective nerve transfers provide an opportunity for restoring the motor function after nerve injuries. Upper-limb robot-assisted therapy has been established as a safe and feasible treatment to complement rehabilitation after neurological injury. The aim of this study is to explore the combined effects of Hand Training with Robotic Glove on fine and gross motor function and activities of daily living in patients after median nerve transfer. The study will be randomized controlled trial. Participants will be recruited through non probability convenience sampling technique. After screening for eligibility, participants will be randomly assigned by balanced pre-randomization into two groups either to a robot-assisted group (RG), participants of this group receiving robot-assisted Hand Rehabilitation with the Syrebo Robotic Gloves or to a control group (CG), receiving dose-matched conventional Hand Rehabilitation without the robot. Participants will be engaged in exercises 4 times a week for 6 weeks, each participants will receive 3 Hand Rehabilitation therapy sessions of 45 Mins per day focusing on hand function. Data will be assessed at the start of the 1st session and at the end of the last session after 6 weeks with the help of Sollerman Hand Function test, Jebsen Taylor Hand Function test, The Original Barthel Index for Activities of Daily living. Data will be analyzed using SPSS version 25
CONDITIONS
Official Title
Effects of Robotic Glove Hand Training in Patients After Median Nerve Transfer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Both genders will be recruited
- Age between 19 to 55 years
- Median nerve transfer after traumatic event (RTA, history of Fall, avulsion, compression or stretch injuries)
- The ability to follow and respond to verbal commands
You will not qualify if you...
- Altered state of consciousness
- Aphasia
- Severe cognitive deficits
- Severe upper limb pathologies of rheumatic nature
- Unable to provide informed consent for the study
- Severe pain in affected arm with visual analogue scale greater than 5
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ghurki Trust Teaching Hospital , Lahore
Lahore, Punjab Province, Pakistan, 54000
Actively Recruiting
Research Team
I
Iqbal Tariq, PhD
CONTACT
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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