Using a robotic glove to help patients recover hand function after nerve surgery
Effects of Robotic Glove Hand Training on Fine and Gross Motor Function and Activities of Daily Living in Patients After Median Nerve Transfer
NA · Riphah International University · NCT06459908
This study tests if using a robotic glove can help people recover better hand function after having surgery on their median nerve compared to regular hand therapy.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 46 (estimated) |
| Ages | 19 Years to 55 Years |
| Sex | All |
| Sponsor | Riphah International University (other) |
| Locations | 1 site (Lahore, Punjab Province) |
| Trial ID | NCT06459908 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of robotic glove-assisted hand training on patients who have undergone median nerve transfer due to injury. Participants will be randomly assigned to either a robotic rehabilitation group, which utilizes the Syrebo Robotic Gloves, or a control group receiving conventional hand rehabilitation. The intervention consists of exercises conducted four times a week for six weeks, focusing on improving fine and gross motor functions as well as daily living activities. The study aims to determine if robotic assistance enhances recovery compared to traditional methods.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 19 to 55 who have undergone median nerve transfer after a traumatic event.
Not a fit: Patients with severe cognitive deficits, altered consciousness, or significant pain in the affected arm may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve hand function and quality of life for patients recovering from median nerve injuries.
How similar studies have performed: Previous studies have shown promising results with robotic-assisted rehabilitation techniques, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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 Exclusion Criteria: subjects will be excluded if they have * Altered state of consciousness, * Aphasia , * Severe cognitive deficits . * Severe pathologies of upper limb of rheumatic nature * Could not provide informed consent for study * Severe pain in affected arm Visual analogue scale \> 5
Where this trial is running
Lahore, Punjab Province
- Ghurki Trust Teaching Hospital , Lahore — Lahore, Punjab Province, Pakistan (RECRUITING)
Study contacts
- Principal investigator: Sabiha Arshad, Mphil — Riphah International University
- Study coordinator: Iqbal Tariq, PhD
- Email: iqbal.tariq@riphah.edu.pk
- Phone: 03458236752
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Median Nerve Injury, Hand Rehabilitation, Nerve transfer Rehabilitation, Robotic Glove