Examining how Carpal Tunnel Syndrome affects daily activities and participation
Investigation of the Effect of Different Severities of Carpal Tunnel Syndrome on Activity and Participation
This study looks at how different levels of Carpal Tunnel Syndrome affect daily activities and participation for people aged 18-65 with the condition.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Kutahya Health Sciences University Academic / other |
| Locations | 1 site (Kutahya) |
| Trial ID | NCT06635109 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the impact of varying severities of Carpal Tunnel Syndrome (CTS) on individuals' activities and participation, using the International Classification of Functioning, Disability and Health (ICF) framework. Participants aged 18-65 diagnosed with CTS in their dominant hand will complete several questionnaires, including the SF-36 and Q-DASH, to assess their functional status. Data will be analyzed using statistical methods such as One-way ANOVA to determine differences between groups based on severity of CTS.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 18-65 who have been diagnosed with Carpal Tunnel Syndrome in their dominant hand.
Not a fit: Patients with systemic inflammatory diseases, diabetes, or other conditions affecting nerve function may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights into how CTS affects patients' daily lives, potentially leading to improved management strategies.
How similar studies have performed: While similar studies have explored the impact of CTS on quality of life, this specific approach using the ICF framework is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosis of CTS in the dominant hand * Being between the ages of 18-65 * Volunteering to participate in the study Exclusion Criteria: * Having systemic inflammatory disease * Having a disease that may cause polyneuropathy such as diabetes mellitus * Having a pacemaker * Having a disease affecting the central nervous system * Having cervical radiculopathy * History of previous operation or local steroid injection due to CTS
Where this trial is running
Kutahya
- Kutahya Health Science University — Kutahya, Turkey (Recruiting)
Study contacts
- Study coordinator: Emrah Afsar, Phd
- Email: emrah.afsar@ksbu.edu.tr
- Phone: 5062527008
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.