Actively Recruiting

Phase Not Applicable
Age: 20Years - 45Years
All Genders
ID06687018

Comparative Effects of Kaltenborn Versus Mulligan Mobilisation on Pain, Disability and Hand Function in Patients With Carpal Tunnel Syndrome

Led by Riphah International University · Updated on 2024-11-13

48

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Carpal Tunnel Syndrome (CTS) is a common condition caused by pressure on the median nerve in the wrist, leading to symptoms like pain, tingling, and numbness, especially during activities such as drawing, typing, or playing video games. Researchers aim to compare the effects of two physical therapy techniques, Kaltenborn and Mulligan mobilisation, on reducing pain, disability, and improving hand function in people with CTS. In this randomized clinical trial, 48 participants will be randomly assigned to receive either Grade 3 Kaltenborn mobilisation or Mulligan mobilisation, both combined with conventional treatment. The conventional treatment includes hot packs for 10 minutes, shortwave diathermy for 5 minutes, and nerve and tendon gliding exercises. Both mobilisation treatments will be administered in three sessions per week over four weeks, with specific protocols for repetitions and sets outlined for each technique. Participants will be assessed before and after the 4-week treatment period using pain and hand function questionnaires, including the Numeric Pain Rating Scale and the Boston Carpal Tunnel Questionnaire. Data will be analyzed to compare pain levels, disability, and hand function between the two groups. The study is sponsored by Riphah International University and will be conducted with ethical approval and monitoring to ensure participant safety throughout the trial.

CONDITIONS

Brief Title

Effects of Kaltenborn and Mulligan Mobilisation in Patients With Carpal Tunnel Syndrome.

Who Can Participate

Age: 20Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Both genders between 20 and 45 years of age
  • Individuals having localized pain, tingling and numbness in the median nerve distribution
  • Positive Tinel sign and positive Phalen's test
Not Eligible

You will not qualify if you...

  • Any sensory and/or motor deficit in either the ulnar or radial nerve traumatic neck injury
  • Previous hand surgery or trauma or cervical radiculopathy
  • Systemic disease e.g. diabetes mellitus or thyroid disease or rheumatoid arthritis

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 4 weeks

Participants receive either Kaltenborn mobilisation or Mulligan mobilisation along with conventional treatment to manage carpal tunnel syndrome symptoms.

Three sessions per week for four weeks

Trial Site Locations

Total: 1 location

1

Ejaz Hospital

Lahore, Punjab Province, Pakistan

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Research Team

I

Imran Amjad, Phd

I

Imran Amjad, Phd

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Effectiveness of Tendon and Nerve Gliding Exercises in the Treatment of Patients With Mild Idiopathic Carpal Tunnel Syndrome: A Randomized Controlled Trial.

Hossein Ali Abdolrazaghi, Mahmoud Khansari, Maryam Mirshahi...

https://pubmed.ncbi.nlm.nih.gov/33855879

Comparison of two manual therapy techniques in patients with carpal tunnel syndrome: A randomized clinical trial.

Ghadam Ali Talebi, Payam Saadat, Yahya Javadian...

https://pubmed.ncbi.nlm.nih.gov/32509244