Effects of Muscle Energy Technique on Neck Disability and Cervical Range of Motion in Individuals With Non-Specific Neck Pain
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Arm 1-Muscle Energy Technique (MET), Arm 2- Standard Electrotherapy.
- Who it may be relevant to
- Registry conditions: Non-specific Neck Pain, Neck Pain. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Turkey (Türkiye)
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
The Effect of Muscle Energy Technique on Neck Disability and Cervical Range of Motion in Patients With Non-Specific Neck Pain
Overview
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.
Detailed description
This study is designed to evaluate the effects of the Muscle Energy Technique (MET) on neck disability and cervical range of motion in individuals with non-specific neck pain. Non-specific neck pain is a common musculoskeletal condition that may lead to functional limitations and reduced quality of life.
The study will be conducted at Avicenna International Hospital in Istanbul. Participants who meet the inclusion criteria will be recruited and evaluated before and after the intervention.
The Muscle Energy Technique will be applied as the primary intervention. Outcome measures will include the Neck Disability Index (NDI) to assess disability level and goniometric measurements to evaluate cervical range of motion.
Pre- and post-intervention comparisons will be performed to determine the effectiveness of the Muscle Energy Technique. The results of this study are expected to provide evidence regarding the clinical effectiveness of MET in the management of non-specific neck pain and contribute to physiotherapy practice.
Interventions
- Behavioral 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-interve - Device 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.
Primary outcome measures
- Neck Disability Index [Time frame: Baseline and at the end of the 10-day treatment period]
Secondary outcome measures (1)
- Cervical Range of Motion [Time frame: Baseline and at the end of the 10-day treatment period]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Turkey (Türkiye) · 1 center
- Avicenna International Hospital — Istanbul
Identifiers
NCT: NCT07524075 · USKU-2026-TCT-01