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Clinical Trials/NCT05466162
NCT05466162
Unknown
Not Applicable

Effects of Soft Tissue Massage Along With Mobilization Technique on Intensity of Symptoms and Functional Status of Carpal Tunnel Syndrome - A Randomized Controlled Trial

Dow University of Health Sciences1 site in 1 country60 target enrollmentSeptember 21, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Carpal Tunnel Syndrome
Sponsor
Dow University of Health Sciences
Enrollment
60
Locations
1
Primary Endpoint
Change in pain intensity on Visual Analog Scale in centimeter after sixth week
Last Updated
3 years ago

Overview

Brief Summary

The objective of this experimental study is to determine the effect of soft tissue massage along with mobilization technique on intensity of pain by visual analog scale and functional status by using Jamar hand-held dynamometer, Pinch Gauge and Boston Scale for carpal tunnel syndrome questionnaire in Carpal tunnel syndrome patients. It is being conducted on patients with Carpal tunnel syndrome at Sindh Institute of Physical Medicine and Rehabilitation, Karachi and Neurological outpatient department of Dr. Ruth K. M. Pfau, Civil Hospital Karachi among Sixty participants with mild and moderate severity of Carpal Tunnel Syndrome will be randomly allocated in two groups after initial screening by a consultant physiatrist according to CTS-6 scale. Written informed consent will be taken from each participant. Group A will be treated with soft tissue massage (Medenci hand massage technique) along with joint (radiocarpal and inter-carpal) and median nerve mobilization slider technique while group B will be treated with joint (radiocarpal and inter-carpal) and median nerve mobilization slider technique only. Participant will be evaluated by visual analog pain scale, Boston scale of carpal tunnel syndrome, dynamometer and -pinch gauge, Center for Epidemiologic Studies Depression Scale and Pain Anxiety Symptoms Scale on day 1 and last treatment session.

Registry
clinicaltrials.gov
Start Date
September 21, 2021
End Date
August 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hamna Syed

Hamna Syed

Dow University of Health Sciences

Eligibility Criteria

Inclusion Criteria

  • Consultant Physiatrist will be diagnosed patients of carpal tunnel syndrome on electro diagnostic test i.e. Nerve Conduction Studies.
  • Mild and moderate severity of Carpal tunnel syndrome.
  • Age: 18-50 years
  • Both gender patients with unilateral involvement of the hand

Exclusion Criteria

  • Exclusion Criteria:
  • In electro diagnostic test, either motor or sensory deficit in the ulnar nerve and radial nerve.
  • Other Neurological problems ( cervical myelopathy, motor neuron disease like amyotrophic lateral sclerosis
  • Neoplasm around the affected arm
  • Presence of other musculoskeletal problems of upper quadrant (for example: rheumatoid arthritis or fibromyalgia, cervical radiculopathy)
  • Any recent history of trauma of upper extremity on affected side

Outcomes

Primary Outcomes

Change in pain intensity on Visual Analog Scale in centimeter after sixth week

Time Frame: At baseline and after completion of study at after sixth week

Visual Analog Scale can be defined as a subjective psychometric response scale used to measure distinct behavioral or physiological phenomena based on linear numerical gradient in pain intensity measurement. The patients rate their pain intensity on 0 to 10 cm where 0 cm refers 'no pain' and 10 cm refers 'most excruciating pain'. Increase in number of cm suggests worst pain.

Change in hand grip strength by using Jamar dynamometer

Time Frame: At baseline and after completion of study at sixth week

Hand grip strength is quantify in kilogram by using Jamar dynamometer. Measurements was taken three times of each individuals and then calculated mean of these readings.

Change in symptoms severity and functional status on scale of Boston Carpal Tunnel Questionnaire in scores

Time Frame: At baseline and after completion of study at after sixth week

It is a self-administered likert scale, containing two parts, namely the symptom severity scale and the functional status scale. It is used to assess the severity of symptoms and evaluate the difficulty in implementing the designated task. Symptom severity scale contains 11 items and the functional status scale contans 8 items. Higher the score in both scales indicating higher severity and more difficulty in performing the task. Scoring for Symptoms severity scale: Less than 11 or 11 = Asymptomatic, 12 to 22 = Mild, 23-33 = Moderate, 24-44 = Severe, 45-55 = Very Severe Scoring for Functional status scale: less than 8 or 8 = Asymptomatic, 9-16 = Mild, 17-24 = Moderate, 25-32 = Severe, 33-40 = Very Severe The total score of both scale is calculated as the mean of the scores for the total items of scale.

Change in pinch strength by using Pinch Gauge

Time Frame: At baseline and after completion of study at sixth week

Pinch grip strength is measured in kilogram by using Pinch Gauge. Measurements was taken three times of each individuals and then calculated mean of these readings.

Study Sites (1)

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