CClinicalTrials.gg
CompletedNCT05460026Updated Apr 6, 2023

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

An interventional study of Routine Physical Therapy and Powerball Exercises in Carpal Tunnel Syndrome, sponsored by University of Lahore. Completed at 1 site in Pakistan. Open to participants aged 45 Years to 60 Years. Per ClinicalTrials.gov, last updated 2023-04-06.

Sponsored by University of Lahore · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Dec 2021, registered Jul 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
86
Allocation
Randomized
Ages
45 Years to 60 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Carpal Tunnel Syndrome

Keywords

  • Physical therapy
  • Median Neuropathy
  • Power Ball Exercise
  • Carpal Tunnel Syndrome
03

In context

Carpal Tunnel Syndrome

589 studies on the registry are indexed under Carpal Tunnel Syndrome; 139 are open to participants now.

This study's enrollment of 86 is above the median of 60 across 445 interventional studies indexed under Carpal Tunnel Syndrome.

Browse Carpal Tunnel Syndrome studies →

Lead sponsor

University of Lahore is the lead sponsor of 223 studies on the registry; 40 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
45 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
86 participants (actual)

Study arms

  • Active comparator
    Group A

    Routine physical therapy will be given to the participants of group A

    Other: Routine Physical Therapy

  • Experimental
    Group B

    Powerball exercises with routine physical therapy will be given to the participants of group B

    Other: Powerball Exercises

Interventions

  • OtherRoutine Physical Therapy

    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).

  • OtherPowerball Exercises

    Participants will be using the Powerball™ for 5 minutes per hand, 3 times a week along with routine physical therapy exercises.

06

What researchers measure

Primary outcomes

  1. Pain Intensity

    Pain Intensity will be measured by Numeric Rating Scale (NRS)

    Time frame: Change in pain will be measured at initial visit, at sixth session and at the twelfth session.

  2. Grip Strength

    Grip Strength will be measured by using handheld dynamometry (HHD)

    Time frame: Change in grip strength will be measured at initial visit, at sixth session and at the twelfth session.

  3. Functional Disability

    Functional disability will be measured by Boston Carpal Tunnel Syndrome Questionnaire (BCTSQ)

    Time frame: Change in functional disability will be measured at initial visit, at sixth session and at the twelfth session.

07

Study locations

1 site
  • The University of Lahore
    Lahore, Punjab 54000, Pakistan
08

References and documents

Individual participant data

Plan to share: Yes — Immediately after publication

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 6, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05460026
Lead sponsor
University of Lahore
Responsible party
Ayesha Jamil (Assistant Professor, University of Lahore) — Principal investigator
First posted
Jul 15, 2022
Start date
Dec 23, 2021
Primary completion
May 23, 2022
Completion
Dec 23, 2022
Last update
Apr 6, 2023

Study contacts

Ashfaq Ahmed, PhD
study director · The University of Lahore

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2023. You cannot join it, but the record below documents what was studied.

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