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Clinical Trials in Turkey / NCT07524075
Recruiting Not applicable

Effects of Muscle Energy Technique on Neck Disability and Cervical Range of Motion in Individuals With Non-Specific Neck Pain

NCT07524075 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-01-01
Last updated
2026-04-13

Condition(s) studied

Non-specific Neck PainNeck Pain

Investigational drug(s) / intervention(s)

Arm 1-Muscle Energy Technique (MET)Arm 2- Standard Electrotherapy

Arm 1-Muscle Energy Technique (MET): Arm 1-The Muscle Energy Technique (MET) will be applied to the cervical region of participants with non-specific neck pain. The technique will involve the patient performing isometric muscle contractions against a therapist-applied resistance, followed by relaxation and stretching. The intervention will aim to reduce neck pain, improve neck disability, and increase cervical range of motion. The treatment will be applied in a standardized protocol over the study period, with pre- and post-intervention assessments conducted.

Arm 2- Standard Electrotherapy: Arm 2 - Standard Electrotherapy Participants in this group will receive a standard electrotherapy protocol applied to the cervical region. The intervention will be administered according to routine clinical practice for non-specific neck pain. Electrotherapy parameters will be applied consistently during the treatment sessions. No Muscle Energy Technique (MET) will be used in this group. Pre- and post-intervention assessments will be conducted to evaluate outcomes.

Study summary

This study aims to investigate the effect of the Muscle Energy Technique on neck disability level and cervical range of motion in individuals with non-specific neck pain. The study will be conducted at Avicenna International Hospital in Istanbul. Participants with non-specific neck pain will be included in the study. The intervention will involve the application of Muscle Energy Technique, and outcomes will be assessed using standardized measures of neck disability and cervical range of motion. The findings are expected to contribute to improving treatment approaches for individuals with non-specific neck pain.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: Age between 18 and 65 years Diagnosis of non-specific neck pain Presence of neck pain for at least 4 weeks Ability to understand and follow instructions Willingness to participate in the study Exclusion Criteria: History of cervical spine surgery Presence of neurological deficits or radiculopathy Specific causes of neck pain (e.g., tumor, infection, fracture) Severe cervical disc herniation Pregnancy Any contraindication to manual therapy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Avicenna International Hospital Istanbul Ataşehir Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07524075 on ClinicalTrials.gov ↗ ← All trials in Turkey