Combined physical and psychological treatment for carpal tunnel syndrome pain
Evaluating the Effectiveness of a Combined Physical and Psychological Intervention in Carpal Tunnel Syndrome Patients With Nociplastic Pain: A Randomized Controlled Trial
This study is testing a new treatment that combines physical therapy and mental health support to see if it can help adults with carpal tunnel syndrome and related pain feel better and function more effectively.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 64 (estimated) |
| Ages | 25 Years to 65 Years |
| Sex | All |
| Sponsor | Ahram Canadian University Academic / other |
| Locations | 1 site (Al Ḩayy Ath Thāmin, Giza) |
| Trial ID | NCT05915611 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of a combined physical and psychological intervention aimed at reducing pain and enhancing function in patients suffering from carpal tunnel syndrome with nociplastic pain. Participants will receive both standard care and the new intervention, which focuses on addressing both physical and psychological aspects of their condition. The study will include adults aged 25-65 who meet specific diagnostic criteria for carpal tunnel syndrome and nociplastic pain as assessed by the Central Sensitization Inventory.
Who should consider this trial
Good fit: Ideal candidates are adults aged 25-65 diagnosed with carpal tunnel syndrome and experiencing nociplastic pain.
Not a fit: Patients who have previously undergone carpal tunnel release surgery or have other upper extremity disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly alleviate pain and improve daily functioning for patients with carpal tunnel syndrome.
How similar studies have performed: While this approach is innovative, similar combined interventions have shown promise in other pain management studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults aged 25-65 years * Both sexes * Diagnosis of carpal tunnel syndrome based on clinical examination and nerve conduction studies * Presence of nociplastic pain as determined by the Central Sensitization Inventory (CSI) with a score ≥40 * Positive tinel and phalen sign. Exclusion Criteria: * Previous carpal tunnel release surgery * Other musculoskeletal or neurological disorders affecting the upper extremity
Where this trial is running
Al Ḩayy Ath Thāmin, Giza
- Outpatient clinic of faculty of physical therapy, Ahram Canadian University — Al Ḩayy Ath Thāmin, Giza, Egypt (Recruiting)
Study contacts
- Study coordinator: Mohamed M ElMeligie, Ph.d
- Email: mohamed.elmeligie@acu.edu.eg
- Phone: +201064442032
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.