Effects of Muscle Energy Technique on Neck Disability and Cervical Range of Motion in Individuals With Non-Specific Neck Pain
MET-NP
The Effect of Muscle Energy Technique on Neck Disability and Cervical Range of Motion in Patients With Non-Specific Neck Pain
1 other identifier
interventional
60
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2026
CompletedFirst Submitted
Initial submission to the registry
April 2, 2026
CompletedFirst Posted
Study publicly available on registry
April 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 15, 2026
April 13, 2026
April 1, 2026
6 months
April 2, 2026
April 9, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Neck Disability Index
Neck disability will be assessed using a validated neck disability questionnaire (e.g., Neck Disability Index - NDI). This scale evaluates the level of disability related to neck pain and daily functional limitations. Neck Disability Index (NDI) score (range: 0 to 50; higher scores indicate greater disability and worse outcome)
Baseline and at the end of the 10-day treatment period
Secondary Outcomes (1)
Cervical Range of Motion
Baseline and at the end of the 10-day treatment period
Study Arms (2)
Muscle Energy Technique Group
EXPERIMENTALParticipants in this group will receive the Muscle Energy Technique (MET) intervention applied to the cervical region. The technique will be used to improve neck disability and increase cervical range of motion in individuals with non-specific neck pain. Pre- and post-intervention assessments will be conducted to evaluate the effectiveness of the intervention.
Control Group
ACTIVE COMPARATORParticipants in this group will receive a standard electrotherapy protocol. The intervention will be applied according to routine clinical practice for individuals with non-specific neck pain. No Muscle Energy Technique (MET) will be applied in this group. Pre- and post-intervention assessments will be conducted.
Interventions
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.
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Avicenna International Hospital
Istanbul, Ataşehir, 34750, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
April 2, 2026
First Posted
April 13, 2026
Study Start
January 1, 2026
Primary Completion (Estimated)
June 30, 2026
Study Completion (Estimated)
July 15, 2026
Last Updated
April 13, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared due to privacy and ethical considerations.