Effect of Dose Variations of High-Power Laser Therapy on Patients With Nonspecific Cervical Pain
NCT ID: NCT07196800
Last Updated: 2025-09-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
60 participants
INTERVENTIONAL
2025-03-10
2025-12-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Laser Therapy for Patients With Nonspecific Neck Pain
NCT07262697
Instrument-Assisted Soft Tissue Mobilization Versus Muscle Energy Technique on Chronic Non-specific Neck Pain
NCT06799130
Effect of Integrated Neuromuscular Inhibition Technique on Subjects with Neck Pain and Forward Head Posture
NCT05439018
The Effect of the Erchonia GVL Low Level Laser Therapy on Neck and Shoulder Pain
NCT04895618
Impact Of Cervical High-Intensity Resistive Exercises In Patients With Chronic Non-Specific Neck Pain
NCT07132229
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
lower dose laser therapy
High intensity laser therapy (low dose) combined with conventional physiotherapy program
840 joules delivered during each session combined with conventional physiotherapy program Participants
higher dose laser therapy
High intensity laser therapy (High dose) combined with conventional physiotherapy program
2632 joules delivered during each session combined with conventional physiotherapy program
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
High intensity laser therapy (low dose) combined with conventional physiotherapy program
840 joules delivered during each session combined with conventional physiotherapy program Participants
High intensity laser therapy (High dose) combined with conventional physiotherapy program
2632 joules delivered during each session combined with conventional physiotherapy program
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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 Criteria
* 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.
18 Years
40 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Deraya University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Deraya university physiotherapy clinic
Minya, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
physio 2 2025
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.