Actively Recruiting

Phase Not Applicable
Age: 25Years - 50Years
All Genders
NCT06980337

Effect of Kendall and Scapulothoracic Exercises in Treatment of Chronic Non-specific Neck Pain

Led by Cairo University · Updated on 2025-07-09

60

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of the clinical trial is to investigate the effect of the combined Kendall and scapulothoracic exercises program on mechanosensitivity of brachial plexus, cervical range of motion, neck functional ability, and craniovertebral angle in patients with chronic non-specific neck pain. we have 3 groups to compare between traditional treatment, scapulothoracic and kendall exercises in treatment of chronic non-specific neck pain.

CONDITIONS

Official Title

Effect of Kendall and Scapulothoracic Exercises in Treatment of Chronic Non-specific Neck Pain

Who Can Participate

Age: 25Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 25 to 50 years
  • Both genders included
  • Chronic neck pain triggered by neck postures, movements, or palpation for at least 3 months
  • Craniovertebral angle less than 54 degrees
  • Body mass index between 25 and 30
Not Eligible

You will not qualify if you...

  • Previous neck injury
  • Previous neck surgery
  • Inflammatory joint disease affecting neck facet joints
  • Neurological disorders such as cervical spondylosis, spondylolisthesis, or disc prolapse
  • Rheumatic diseases
  • Cancer
  • Use of pain medication or physical therapy for neck pain within the last 3 months
  • Inability to perform the exercise program

AI-Screening

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Trial Site Locations

Total: 1 location

1

Physical therapy College - Cairo university

Cairo, Egypt

Actively Recruiting

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Research Team

D

Doaa Rafat Assistant professor of physical therapy - Cairo university, Assistant professor

CONTACT

R

Rania Reda Assistant professor of physical therapy - Cairo university, Assistant professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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