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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04187677
Other study ID # Study-1
Secondary ID Halil Ibrahim Er
Status Recruiting
Phase N/A
First received
Last updated
Start date July 27, 2018
Est. completion date May 15, 2020

Study information

Verified date December 2019
Source Sanko University
Contact Halil Ibrahim ERGEN
Phone 0905437202727
Email hiergen@sanko.edu.tr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to determine the benefits of sensory training for participants who are included in rehabilitation after carpal tunnel surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date May 15, 2020
Est. primary completion date March 15, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- SANKO University Health Practice and Research Center, Orthopedics and Traumatology Unit underwent open carpal tunnel loosening surgery.

Exclusion Criteria:

- The presence of nerve entrapment other than the median nerve (any sensory / motor deficits in the ulnar or radial nerve),

- Wrist injury history (fractures, carpal instabilities),

- Previous surgery in the hand or wrist region,

- Traumatic and recurrent Carpal Tunnel Syndrome, inflammation of the tendon sheath or the presence of general active inflammation

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Sensory Training
The sensory training group includes sensory-oriented interventions and exercises unlike the other classical hand therapy group.
Other:
classical hand therapy
classical hand therapy

Locations

Country Name City State
Turkey SANKO University Gaziantep

Sponsors (1)

Lead Sponsor Collaborator
Sanko University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Joint Position Matching In our study, the wrist joint's range of motion will be evaluated in 2 different directions (flexion / extension and radial / ulnar deviation) for proprioception evaluation. For evaluations of all directions, the individual will be required to bring the wrist to the end of the movement, then to perform half the normal range of motion, while the wrist is in a hanging position from the table edge to allow full movement. The difference between the angular value and the angular value created by the individual will be noted by looking at the angular value on the fixed goniometer. Baseline (First day)
Primary Purdue Pegboard Test The Purdue Pegboard Test is a neuropsychological test of manual dexterity and bimanual coordination. Baseline (First day)
Primary Activity Limitation The Patient-Specific Functional Scale is a self-reported, patient-specific outcome measure, designed to assess functional change, primarily in patients presenting with musculoskeletal disorders. The scale was developed by Stratford et al 1995 as a self-report measure of function that could be used in patients with varying levels of independence. It was designed to provide clinicians with a valid, reliable, responsive, and efficient outcome measure that would be easy to use and applicable to a large number of clinical presentations. Baseline (First day)
Primary Health-Related Quality of Life The EuroQoL-five-dimension (EQ-5D) is one of the most commonly used questionnaires to elicit health state utilities, having both a youth and an adult version. For general populations of adults two versions of the questionnaire have been developed, 3L and 5L, with the latter offering a more detailed description of health status. In order to use the EQ-5D to estimate quality-adjusted life-years, a value set to reflect people's preferences for different health states is needed. Baseline (First day)
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