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Evaluation of Joint Position Sense in Carpal Tunnel Syndrome

P

Pamukkale University

Status

Completed

Conditions

Carpal Tunnel Syndrome

Treatments

Device: Baseline Electrıgoniometer
Device: KForce Sens

Study type

Interventional

Funder types

Other

Identifiers

NCT06048861
E-60116787-020-136447

Details and patient eligibility

About

The aim of the study was to investigate the validity and reliability of the KForce Sens® for the evaluation of wrist joint position sense in individuals with CTS. Wrist joint position sense was assessed with KForce Sens® and Baseline® electrogoniometer. The validity and reliability of the KForce Sens® for wrist position sense evaluation were investigated by comparing the two data sets.

Enrollment

70 patients

Sex

All

Ages

22 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • mild to moderate CTS confirmed with EMG
  • having symptoms for at least 3 months
  • not receiving medical treatment and physiotherapy until 3 months before the study at the latest

Exclusion criteria

  • having trauma in the affected extremity in the last 6 months
  • having cervical radiculopathy
  • having brachial plexopathy
  • having cognitive problems
  • having neurological problems
  • being pregnant

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

70 participants in 2 patient groups

Individuals with Carpal Tunnel Syndrome
Experimental group
Treatment:
Device: KForce Sens
Device: Baseline Electrıgoniometer
Healthy Controls
Experimental group
Treatment:
Device: KForce Sens

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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