Skip to main content
OpenTrials
Completed

NCT Number: NCT07643740

COMPARATIVE EFFECTS OF DRY NEEDLING AND NEURAL MOBILIZATION ON PAIN, STRENGTH AND RANGE OF MOTION IN PATIENTS WITH GOLFER'S ELBOW

This randomized clinical trial aims to compare the effectiveness of Dry Needling and Neural Mobilization in patients diagnosed with Golfer's Elbow (Medial Epicondylitis). The study will evaluate the effects of both interventions on pain intensity, grip strength, and range of motion. Participants will be randomly allocated to either the Dry Needling group or the Neural Mobilization group and treated over a specified intervention period. Outcome measures will be assessed at baseline and after treatment to determine which intervention provides greater improvement in pain reduction, muscle strength, and functional mobility. The results may contribute to evidence-based rehabilitation strategies for managing Golfer's Elbow

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Green International University

Lahore, Punjab Province, 54000, Pakistan

About this study

Golfer's Elbow (Medial Epicondylitis) is a common musculoskeletal disorder characterized by pain and tenderness over the medial epicondyle of the elbow, often associated with repetitive wrist flexion and forearm pronation activities. The condition can lead to decreased grip strength, restricted range of motion, and impaired functional performance, affecting daily activities and quality of life.

Various physiotherapy interventions have been used for the management of Golfer's Elbow, including Dry Needling and Neural Mobilization. Dry Needling is a technique that targets myofascial trigger points to reduce pain, improve blood flow, and restore muscle function. Neural Mobilization aims to restore the normal mobility and physiological function of peripheral nerves by reducing neural tension and improving neural mechanics.

The purpose of this randomized clinical trial is to compare the effectiveness of Dry Needling and Neural Mobilization in reducing pain, improving grip strength, and increasing range of motion in patients with Golfer's Elbow. Eligible participants will be randomly assigned to one of two intervention groups. Baseline assessments will be conducted before treatment, followed by post-intervention assessments after completion of the treatment protocol.

Primary outcome measures will include pain intensity, assessed using a validated pain scale, while secondary outcomes will include grip strength and elbow/wrist range of motion. Data collected will be analyzed to determine whether one intervention demonstrates superior clinical outcomes compared to the other.

The findings of this study are expected to provide evidence regarding the comparative effectiveness of these commonly used physiotherapy interventions and may assist clinicians in selecting appropriate treatment strategies for patients with Golfer's Elbow.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • • Both male and female patients were included.
  • Diagnosis of Medial Epicondylitis by spiral test clinically confirmed by orthopaedic.

pain is limited on medial epicondyle

  • Pain reproduced with resisted wrist flexion and/or forearm pronation.
  • Aged between 18-40 years
  • Acute to Subacute stage (≥ 6 weeks and ≤ 12 months
  • NPRS score ≥ 4/10 at baseline

Exclusion criteria

  • • History of Other elbow pathologies e.g (Lateral epicondylitis , Olecranon bursitis ,Ligament injuries)
  • Radial or ulnar neuropathies not associated with medial epicondylitis.
  • Systemic or inflammatory conditions affecting tendons, such as rheumatoid arthritis
  • Diabetes with neuropathy (unless controlled and neuropathy absent)
  • Previous surgical procedures around the elbow or wrist within the past 6 months
  • Corticosteroid injection, PRP or shockwave therapy within the last 3 months

Treatment and study plan

dry needling

Procedure

Participants will receive dry needling to the affected forearm muscles along with conventional physiotherapy. Treatment will be administered twice weekly for 6 weeks, totaling 12 sessions. Outcomes will include pain, grip strength, and range of motion

neural mobilization

Procedure

Participants will receive neural mobilization techniques along with conventional physiotherapy. Treatment will be administered twice weekly for 6 weeks, totaling 12 sessions. Outcomes will include pain, grip strength, and range of motion.

Primary outcomes

  1. Pain intensity

    Time frame: Baseline and at 6 weeks post-intervention

    Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS). The scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores represent greater pain intensity.

Secondary outcomes

  1. Grip strength

    Time frame: Baseline and at 6 weeks post-intervention

    Grip strength will be measured using a hand dynamometer. Higher values indicate greater muscle strength.

  2. Range of motion

    Time frame: Baseline and at 6 weeks post-intervention

    Elbow and wrist range of motion will be measured using a standard goniometer. Higher values indicate improved joint mobility.

Sponsors and collaborators

Lead sponsor

Green International University

Other

Registry information

Acronym: DN-NM-GE

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 11, 2026
Registry last updated
Jun 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.