Effects of Pain Neuroscience Education on Carpal Tunnel Syndrome
Effects of Pain Neuroscience Education and Standard Rehabilitation Regime in Patients of Carpal Tunnel Syndrome
This study is testing if adding Pain Neuroscience Education to regular rehab helps people with Carpal Tunnel Syndrome feel better and recover faster than just rehab alone.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 20 Years to 50 Years |
| Sex | Female |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Lahore, Punjab Province) |
| Trial ID | NCT06509633 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of Pain Neuroscience Education (PNE) combined with standard rehabilitation on patients suffering from Carpal Tunnel Syndrome (CTS). It aims to determine whether PNE can enhance recovery and pain relief compared to standard rehabilitation alone. The study involves a randomized, double-blind design where participants will receive either PNE plus rehabilitation exercises or rehabilitation exercises only. The goal is to provide high-quality evidence on the effectiveness of this combined approach for CTS management.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 20 to 40 years with a medical diagnosis of moderate to severe Carpal Tunnel Syndrome and symptoms present for at least one month.
Not a fit: Patients with neurological conditions affecting the central nervous system or those who have undergone previous surgery on the affected upper limb may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management and functional recovery for patients with Carpal Tunnel Syndrome.
How similar studies have performed: Previous studies have shown positive results with similar approaches, indicating potential effectiveness, although more research is needed in this specific area.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * age between 20\_40 years old. * Medical diagnosis of moderate to severe CTS. * Symptoms of CTS since 1month * Unilateral or bilateral symptoms * Availability and access to the hospital. Exclusion Criteria: * Inability to understand instructions, neurological conditions of the central nervous system (e.g. stroke, spinal cord injury) * Patients on treatment with alternative therapies * Previous participation in a research program * Previous surgery on the affected upper limb
Where this trial is running
Lahore, Punjab Province
- Absaar medical center — Lahore, Punjab Province, Pakistan (Recruiting)
Study contacts
- Principal investigator: Saba khan — Riphah International University
- Study coordinator: Imran Amjad
- Email: Imran.amjad@riphah.edu.pk
- Phone: 03324390125
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.