- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05460026
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
Status
Completed
Conditions
Intervention / Treatment
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:
- Age group 45-60 years
- Both male and female
- Clinically diagnosed carpal tunnel syndrome
- Carpal Tunnel Syndrome for a duration of more than 02 months
- Tingling sensation and numbness over the dorsal surface of thumb, index, middle, and lateral 1/3rd of ring fingers
- Positive Tinel's sign
- Positive Phalen's Maneuver
Exclusion Criteria:
- Any previous trauma, fracture, subluxation, dislocation, surgery or bony abnormalities around wrist joint in the past 5 years.
- Symptomatic Arthritis of wrist joint
- Cervical radiculopathy
- 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.
Sponsor
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- Muhammad Jahanzaib Rasool
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.
Clinical Trials on Carpal Tunnel Syndrome
-
Stanford UniversityMayo Clinic; National Institute of Arthritis and Musculoskeletal and Skin Diseases... and other collaboratorsCompletedCarpal Tunnel Syndrome | Carpal Tunnel | Carpal Tunnel Syndrome Bilateral | Carpal Tunnel Syndrome Left | Carpal Tunnel Syndrome RightUnited States
-
Issa, Abdulhamid Sayed, M.D.CompletedCarpal Tunnel Syndrome | CTS | Carpal Tunnel Release | Carpal Tunnel Surgery | Carpal Tunnel Transverse ApproachSyrian Arab Republic
-
Kuopio University HospitalUniversity of Eastern FinlandNot yet recruitingCarpal Tunnel Syndrome (CTS) | Carpal Tunnel SurgeryFinland
-
University of Sao Paulo General HospitalRecruitingCarpal Tunnel Syndrome (CTS) | Carpal Tunnel SurgeryBrazil
-
Maasstad HospitalRecruitingCarpal Tunnel Syndrome (CTS) | Lacertus SyndromeNetherlands
-
Galala UniversityCompletedCarpal Tunnel Syndrome (CTS)Egypt
-
Stanford UniversityCompletedCarpal Tunnel Syndrome (CTS)United States
-
Fundacin Biomedica Galicia SurCompletedCarpal Tunnel Syndrome (CTS)Spain
-
GCS Ramsay Santé pour l'Enseignement et la RechercheCompletedCarpal Tunnel Syndrome (CTS) | Heel Pain SyndromeFrance
-
Ankara UniversityNot yet recruitingCarpal Tunnel Syndrome (CTS)Turkey (Türkiye)
Clinical Trials on Routine Physical Therapy
-
Riphah International UniversityCompleted
-
Riphah International UniversityCompleted
-
Riphah International UniversityCompletedCerebral PalsyPakistan
-
University of LahoreRecruitingMild Traumatic Brain InjuryPakistan
-
University of LahoreRecruitingChronic Hemorrhagic StrokePakistan
-
University of LahoreRecruitingHemiplegic Cerebral PalsyPakistan
-
Riphah International UniversityCompleted
-
Riphah International UniversityEnrolling by invitation
-
University of LahoreCompleted
-
University of LahoreRecruiting