Effectiveness of Desensitisation and Pain Neuroscience Education in Patients With Carpal Tunnel Syndrome With Nosiplastic Pain

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorKutahya Health Sciences University

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

Being diagnosed with CTS

Being suitable for the nosiplastic pain phenotype

Being between the ages of 18-65

Volunteering to participate in the study

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • Desensitisation

    Other intervention

    This technique is utilized to decrease, or normalize, the body's response to particular sensations.

  • Pain neuroscience education

    Other intervention

    PNE is an educational intervention aiming to alter a patient's beliefs and cognitions regarding their pain experience.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Group 1 (desensitisation)Active comparator 1 intervention
Group B: Group 2 (desensitisation and pain neuroscience education)Active comparator 2 interventions

Trial outcomes

Primary outcomes

1

Pressure Paın Threshold Measurement

The pressure pain threshold (PPT), the minimum amount of pressure at which the pressure sensation changes to pain, is measured with an electronic algometer (median nerve, ulnar nerve and radial nerve, C5-C6 zygapophyseal joint level (proximal), and tibialis anterior). Participants are asked to report when the sensation changes from pressure to pain. The mean of the three trials is calculated (with a 30 s rest interval in between).

Time frame
[at the beginning of the study] [At the end of 6 weeks] [3 months later]
2

Boston Carpal Tunnel Questionnaire - Symptom Severity Scale

Boston Carpal Tunnel Questionnaire - Symptom Severity Scale is an 11-item questionnaire used to assess symptom severity in individuals with CTS. Each item is scored from 1 to 5. Scores range from 1 (no symptoms) to 5 (worst symptoms). The patient's symptom severity score is the average score of 11 items.

Time frame
[at the beginning of the study] [At the end of 6 weeks] [3 months later]
3

Boston Carpal Tunnel Questionnaire - Functional Status Scale

Boston Carpal Tunnel Questionnaire - Functional Status Scale is an 8-item questionnaire used to assess the functional status of patients with CTS. Each item is scored from 1 to 5. Scores range from 1 (no functional deficit) to 5 (worst possible function). The patient's functional status score is the average of all 8 items.

Time frame
[at the beginning of the study] [At the end of 6 weeks] [3 months later]
4

Pain Catastrophising Scale

The Catastrophising Pain Scale (PCS) is used to measure catastrophising in response to pain through 13 statements with four possible options from 1 "never" to 4 "always". Higher scores indicate greater catastrophised pain.

Time frame
[at the beginning of the study] [At the end of 6 weeks] [3 months later]

Secondary outcomes

1

Cold Pain Threshold

For cold pain threshold, ice cubes (-5°C) placed in a plastic bag will be placed on the patients' skin for 10 seconds. Increased sensory perception will be considered as gain of function. The intensity of pain will also be recorded on an NRS scale ranging from 0 (no pain) to 10 (worst pain imaginable).

Time frame
2 minutes
2

Hot Pain Threshold

Thermal pain perception will be tested using a 3 cm2 sized metal piece equal to (lab-QST thermode size). The metal parts will be heated to 45˚C for hot pain threshold. The metal pieces will be applied to the skin for 3 seconds. It will be determined whether the stimulus is painful (yes/no), and if painful, the intensity of the pain on a numerical rating scale (NRS) (0: no pain, 10: imaginably worse pain).

Time frame
2 minutes
3

Pressure Pain Threshold

A digital algometer will be used to measure Pressure Pain Threshold levels. Pressure will be applied at a rate of approximately 30 kPa/s with the algometer placed perpendicular to the point of application. Participants will be instructed to report when the sensation changes from pressure to pain. The intensity of pain will also be recorded on an NRS scale ranging from 0 (no pain at all) to 10 (worst pain imaginable).

Time frame
3 minutes
4

Mechanical Pain Threshold

Mechanical pain threshold: to be assessed with a toothpick and a von Frey filament (256 mN). Increased sensory perception will be considered to reflect gain of function. The intensity of pain will also be recorded on an NRS scale ranging from 0 (no pain at all) to 10 (worst pain imaginable).

Time frame
3 minutes

Other outcomes

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