Effects Of Power Ball Exercises In Addition To Routine Physical Therapy In Patients With Carpal Tunnel Syndrome

April 5, 2023 updated by: Ayesha Jamil, University of Lahore

Effects Of Power Ball Exercises In Addition To Routine Physical Therapy On Pain, Grip Strength And Functional Disability In Patients With Carpal Tunnel Syndrome

The purpose for doing this study is to determine that whether use of Power Ball in form of resistance training will be effective in increasing grip strength in carpel tunnel syndrome patient and possible benefits of the regime as effective means of rehabilitation for wrist and hand injuries. Moreover for increasing grip strength it can be used as an adjunct for physical therapy treatment.

Study Overview

Study Type

Interventional

Enrollment (Actual)

86

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Punjab
      • Lahore, Punjab, Pakistan, 54000
        • The University of Lahore

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

45 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Age group 45-60 years
  2. Both male and female
  3. Clinically diagnosed carpal tunnel syndrome
  4. Carpal Tunnel Syndrome for a duration of more than 02 months
  5. Tingling sensation and numbness over the dorsal surface of thumb, index, middle, and lateral 1/3rd of ring fingers
  6. Positive Tinel's sign
  7. Positive Phalen's Maneuver

Exclusion Criteria:

  1. Any previous trauma, fracture, subluxation, dislocation, surgery or bony abnormalities around wrist joint in the past 5 years.
  2. Symptomatic Arthritis of wrist joint
  3. Cervical radiculopathy
  4. Corticosteroid injection within 3 months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Group A
Routine physical therapy will be given to the participants of group A
Participants will receive routine physical therapy which includes ultrasound, nerve gliding, tendon mobilization, stretching, mobility and strengthening exercises for the wrist. Each session will last for 30 minutes with 12 sessions on alternate days (3 sessions / week).
Experimental: Group B
Powerball exercises with routine physical therapy will be given to the participants of group B
Participants will be using the Powerball™ for 5 minutes per hand, 3 times a week along with routine physical therapy exercises.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain Intensity
Time Frame: Change in pain will be measured at initial visit, at sixth session and at the twelfth session.
Pain Intensity will be measured by Numeric Rating Scale (NRS)
Change in pain will be measured at initial visit, at sixth session and at the twelfth session.
Grip Strength
Time Frame: Change in grip strength will be measured at initial visit, at sixth session and at the twelfth session.
Grip Strength will be measured by using handheld dynamometry (HHD)
Change in grip strength will be measured at initial visit, at sixth session and at the twelfth session.
Functional Disability
Time Frame: Change in functional disability will be measured at initial visit, at sixth session and at the twelfth session.
Functional disability will be measured by Boston Carpal Tunnel Syndrome Questionnaire (BCTSQ)
Change in functional disability will be measured at initial visit, at sixth session and at the twelfth session.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Ashfaq Ahmed, PhD, The University of Lahore

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 23, 2021

Primary Completion (Actual)

May 23, 2022

Study Completion (Actual)

December 23, 2022

Study Registration Dates

First Submitted

July 1, 2022

First Submitted That Met QC Criteria

July 12, 2022

First Posted (Actual)

July 15, 2022

Study Record Updates

Last Update Posted (Actual)

April 6, 2023

Last Update Submitted That Met QC Criteria

April 5, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Immediately after publication

IPD Sharing Time Frame

Beginning 9 months and ending on 36th month

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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