Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT05689788

High-intensity Laser Therapy for Neck Pain

Led by Quiropraxia y Equilibrio · Updated on 2025-08-07

72

Participants Needed

2

Research Sites

91 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chronic nonspecific neck pain is a common musculoskeletal disorder recognized for its high rates of disability and economic losses, ranking second in musculoskeletal conditions after low back pain. There are several effective physical therapy interventions to treat chronic nonspecific neck pain, such as laser therapy. High-intensity laser therapy (HILT) is a recent treatment proposed to reduce musculoskeletal pain; however, there are few studies that prove its effects in reducing neck pain. The aim of this randomized clinical trial is to evaluate the effect of high-intensity laser therapy on pain intensity in patients with chronic nonspecific neck pain. The research will be carried out in the laboratory of physical agents at the Andrés Bello University, Campus Casona de las Condes. Participants will be employers and volunteer students with non-specific chronic neck pain. Participants will be randomized and allocated into 2 study groups: group 1 (HILT and stretching exercises) and group 2 (simulated HILT and stretching exercises). Treatments will be performed twice a week for 4 weeks with 3 assessments: before treatment, at the end of treatment, and 12 weeks after treatment (follow-up). The main results will be the differences in pain pressure threshold (ΔPPT), intensity of pain at rest (ΔRPI) and intensity of pain on movement (ΔMPI). Secondary outcome measures, on the other hand, will include differences in cervical spine range (ΔCROM) and cervical disability (ΔND).

CONDITIONS

Official Title

High-intensity Laser Therapy for Neck Pain

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants must be at least 18 years old.
  • Both men and women can participate.
  • Must have non-specific chronic neck pain lasting 3 months or more.
  • Neck disability index (NDI) score of 5 or higher.
  • Neck pain intensity of 3 or greater on a numerical pain scale.
Not Eligible

You will not qualify if you...

  • Recent neck or shoulder injuries in the last 3 months such as fractures, sprains, tendinopathies, dislocations, or muscle tears.
  • Presence of osteosynthesis materials near the neck or shoulders.
  • Skin wounds or conditions like psoriasis, scars, or burns in the neck or shoulder area.
  • Permanent use of analgesic, anti-inflammatory, or muscle relaxant medication.
  • Neurological issues like loss of sensation, weakness, or color changes in the neck or arms.
  • Diagnosed photosensitivity or adverse reactions to sunlight.
  • Presence of dermatomyositis, systemic lupus erythematosus, hepatic porphyria, cutaneous carcinoid syndrome, or pellagra.
  • Diagnosis of cancer or tumors within the last 5 years.
  • Epilepsy.

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

Universidad Andrés Bello

Santiago, Las Condes, Chile, 7591538

Actively Recruiting

2

Hernán Andrés de la Barra

Santiago, Chile

Actively Recruiting

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Research Team

H

Hernán A de la Barra Ortiz, MSc

CONTACT

L

Luis A Gomez Miranda, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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