Effects of Pain Neuroscience Education and Standard Rehabilitation Regime in Patients of Carpal Tunnel Syndrome

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-50
SponsorRiphah International University

About this trial

The aim of this study is to check the effects of Pain Neuroscience education and standard rehabilitation regime in patients of carpal tunnel syndrome.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

age between 20_40 years old.

Medical diagnosis of moderate to severe CTS.

Symptoms of CTS since 1month

Unilateral or bilateral symptoms

Disqualifiers

Inability to understand instructions, neurological conditions of the central nervous system (e.g. stroke, spinal cord injury)

Patients on treatment with alternative therapies

Previous participation in a research program

Previous surgery on the affected upper limb

Trial design

Design model

Parallel

Treatments tested in this trial

  • Pain Neuroscience education and standard rehabilitation regime

    Other intervention

    Median nerve gliding exercises, wrist and forearm muscle stretches, wrist mobilizations and finger joint mobilizations

  • standard Rehabilitation regime

    Other intervention

    standard Rehabilitation regime

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: Pain Neuroscience education and Standard Rehabilitation regimeExperimental treatment 1 intervention
Group B: standard Rehabilitation regimeActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Numeric pain rate scale (NPRS)

Patient level of pain will be assessed using this scale. This scale ranges from 0 to 10. 0 indicates "no pain" and 10 indicates "worst pain.

Time frame
4th week

Secondary outcomes

1

Pain Catastrophizing Scale (PCS)

The Pain Catastrophizing Scale (PCS) was used to measure catastrophic thinking in response to pain through 13 statements with four possible options, from 1 "not at all" to 4 "all the time".

Time frame
4th week

Other outcomes

1

Boston Carpal Tunnel Questionnaire (BCTQ)

BCTQmeasures self reported functional status and severity of symptom. The BCTQ-SSS consists of 11 questions, each question provides 5 response choices, from 1 (no symptoms) to 5 (most severe/often).

Time frame
4th week
2

Goniometer

The range of motions like flexion extension radial deviation and ulnar deviation of wrist will be measured by Goniometer.

Time frame
4th week

Sponsors and contacts

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