RecruitingNot ApplicableNCT07196800

Effect of Dose Variations of High-Power Laser Therapy on Patients With Nonspecific Cervical Pain


Sponsor

Deraya University

Enrollment

60 participants

Start Date

Mar 10, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Nonspecific neck pain, defined as pain without a specific underlying pathology, is a common musculoskeletal disorder that affects a significant proportion of the global population. Neck pain often results in considerable discomfort and functional limitations, impacting individuals' quality of life and ability to perform daily tasks. Estimates suggest that up to 30% of adults experience neck pain annually. The condition ranks among the top causes of disability worldwide, contributing to substantial personal and societal burdens, including lost work productivity and increased healthcare costs.


Eligibility

Min Age: 18 YearsMax Age: 40 Years

Inclusion Criteria5

  • unilateral or bilateral CNP
  • Experiencing moderate to severe neck pain, defined as a Visual Analog
  • Scale (VAS) score of ≥4.
  • Cervical Range of Motion (ROM) Limitation: Documented restriction in cervical ROM compared to normal values for age and gender, to ensure the condition's impact on functional mobility
  • Patients agreed not to take any medication(anti-inflammatories, analgesics, or muscle relaxants) throughout the course of the study or receive any type of treatment for neck pain

Exclusion Criteria5

  • Previous Cervical Surgery: Patients with a history of cervical spine surgery will be excluded to eliminate potential influences from post-surgical changes on the outcomes
  • Diagnosed with cervical disc prolapse as confirmed by clinical evaluation and imaging studies (MRI or CT scans).
  • History of malignancy in the cervical region or other serious medical conditions.
  • Severe comorbidities that may affect treatment outcomes (e.g., uncontrolled diabetes, cardiovascular diseases).
  • Pregnancy or lactation.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

RADIATIONHigh intensity laser therapy (low dose) combined with conventional physiotherapy program

840 joules delivered during each session combined with conventional physiotherapy program Participants

PROCEDUREHigh intensity laser therapy (High dose) combined with conventional physiotherapy program

2632 joules delivered during each session combined with conventional physiotherapy program


Locations(1)

Deraya university physiotherapy clinic

Minya, Egypt

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07196800


Related Trials