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NCT Number: NCT06509633

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

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

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Key information

Age range

20 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Absaar medical center

Lahore, Punjab Province, 56300, Pakistan

Location status: Recruiting

Location contact

Iqra khan

CONTACT

[email protected]

03354671744

Sara Abdulhaq

PRINCIPAL_INVESTIGATOR

About this study

In 2017 a stud assessed effectiveness of standard conservative protocol of CTS and nerve mobilization along with and without PNE and documented that standard conservative care seems to be the most appropriate option for pain relief, although neuroscience education might be a complementary option to accelerate recovery of function. More high-quality research is still necessary to determine its effectiveness and the subgroups of patients who may respond better to this treatment.

In 2019 a study was done to assess the effect of PNE and standard rehabilitation exercises on the 41 patients of CTS. The experimenting group was given one session of PNE plus exercises and the control group was given exercise therapy only. Patients were randomly allocated and double blinded. The analysis of study showed better results with experimental group rather than control group.

Many studies have found the effects of standard rehabilitation of Carpal Tunnel syndrome and their results in controlling pain and dysfunction. However as per researchers' knowledge little literature is available on effects of pain neuroscience education and standard rehabilitation regime in carpal tunnel syndrome. Therefore, this study6 is going to determine the effects of effectiveness of Pain Neuroscience education and standard rehabilitation regime in patients of carpal tunnel syndrome.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age between 20_40 years old.
  • Medical diagnosis of moderate to severe CTS.
  • Symptoms of CTS since 1month
  • Unilateral or bilateral symptoms
  • Availability and access to the hospital.

Exclusion criteria

  • 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

Treatment and study plan

Pain Neuroscience education and standard rehabilitation regime

Other

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

Other names: Standard Rehabilitation regime

standard Rehabilitation regime

Other

standard Rehabilitation regime

Primary outcomes

  1. Numeric pain rate scale (NPRS)

    Time frame: 4th week

    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.

Secondary outcomes

  1. Pain Catastrophizing Scale (PCS)

    Time frame: 4th week

    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".

Other outcomes

  1. Boston Carpal Tunnel Questionnaire (BCTQ)

    Time frame: 4th week

    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).

  2. Goniometer

    Time frame: 4th week

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

Study contacts

Contact information is provided by the study sponsor or research team.

Imran Amjad

CONTACT

[email protected]

03324390125

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jul 19, 2024
Registry last updated
Jul 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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