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Clinical Trials/NCT07566637
NCT07566637CompletedNot Applicable

Low-Intensity Laser Therapy Versus Proprioceptive Neuromuscular Facilitation for Pain and Disability in Chronic Non-Specific Neck Pain: A Randomized Controlled Trial

Istanbul Gedik University1 site in 1 country75 target enrollmentStarted: February 5, 2024Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
75
Locations
1

Study Overview

Brief Summary

This study aimed to investigate and compare the effects of low-intensity laser therapy, a photobiomodulation treatment, and proprioceptive neuromuscular facilitation on pain and disability in individuals with non-specific neck pain. This randomized controlled trial used the Numerical Pain Scale (primary outcome) and the Bournemouth Neck Pain Questionnaire to assess pain, a manual algometer to assess pain threshold, and the Neck Disability Index to assess disability. Three groups were included in this randomized controlled trial: Group 1: Photobiomodulation therapy (low-intensity laser therapy) + conventional physiotherapy; Group 2: Proprioceptive neuromuscular facilitation with stretching and strengthening + conventional physiotherapy; Group 3: Conventional physiotherapy only. We hypothesized that low-intensity laser therapy and proprioceptive neuromuscular facilitation would have distinct effects on pain and disability in chronic non-specific neck pain.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Volunteering to participate in the study
  • A neck pain score of at least 3 on the Numerical Pain Scale in the assessment conducted prior to inclusion in the study
  • A Neck Disability Index score of 5 or higher
  • No comorbid conditions affecting the orthopaedic, neurological or cardiopulmonary systems
  • Participants who have not been enrolled in another clinical trial within the last month

Exclusion Criteria

  • Individuals who have undergone upper limb surgery (e.g. shoulder blade, shoulder, elbow, hand, wrist, etc.) within the last year
  • Individuals with a pacemaker or subcutaneous implant
  • Pregnant women or women who have recently given birth
  • Use of antidepressants, anti-inflammatory drugs or anxiolytics within the last 6 months

Investigators

Sponsor
Istanbul Gedik University
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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