Carpal Tunnel Syndrome Clinical Trials

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Determination of the Effectiveness of Desensitisation and Pain Neuroscience Training in Patients With Carpal Tunnel Syndrome With Nosiplastic Pain Phenotype

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The aim of our study was to determine the effectiveness of desensitisation and pain neuroscience education in a group of patients with mixed phenotype pain (neuropathic and nosiplastic).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Being diagnosed with CTS

• Being suitable for the nosiplastic pain phenotype

• Being between the ages of 18-65

• Volunteering to participate in the study

Locations
Other Locations
Turkey
Kutahya Health Science University
RECRUITING
Kütahya
Contact Information
Primary
Emrah Afsar, Phd
emrah.afsar@ksbu.edu.tr
5062527008
Backup
Ayse Kocak Sezgin, Phd
ayse.kocaksezgin@ksbu.edu.tr
+90 5072243706
Time Frame
Start Date: 2024-10-25
Estimated Completion Date: 2027-06-10
Participants
Target number of participants: 40
Treatments
Active_comparator: Group 1 (desensitisation)
Group 1 will receive desensitisation.
Active_comparator: Group 2 (desensitisation and pain neuroscience education)
Group 2 will receive desensitisation and pain neuroscience education.
Sponsors
Leads: Kutahya Health Sciences University

This content was sourced from clinicaltrials.gov