NCT07524075

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress65%
Jan 2026Jul 2026

Study Start

First participant enrolled

January 1, 2026

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

April 2, 2026

Completed
11 days until next milestone

First Posted

Study publicly available on registry

April 13, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2026

Expected
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 15, 2026

Last Updated

April 13, 2026

Status Verified

April 1, 2026

Enrollment Period

6 months

First QC Date

April 2, 2026

Last Update Submit

April 9, 2026

Conditions

Keywords

Neck PainNon-Specific Neck PainMuscle Energy TechniqueCervical Range of MotionNeck Disability

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

EXPERIMENTAL

Participants 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.

Behavioral: Arm 1-Muscle Energy Technique (MET)

Control Group

ACTIVE COMPARATOR

Participants 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.

Device: Arm 2- Standard Electrotherapy

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.

Control Group

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.

Muscle Energy Technique Group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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)

RECRUITING

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: This study is designed as a single-group interventional study. Participants diagnosed with non-specific neck pain will be evaluated before and after the intervention. The Muscle Energy Technique (MET) will be applied as the primary intervention. No control group will be included in this study. Pre- and post-intervention measurements will be used to assess changes in neck disability and cervical range of motion. The outcomes will be compared within the same group to determine the effectiveness of the intervention.
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.

Locations