Non-specific Neck PainMET-NPNCT07524075
Effects of Muscle Energy Technique on Neck Disability and Cervical Range of Motion in Individuals With Non-Specific Neck Pain
A study testing Arm 1-Muscle Energy Technique (MET) and Arm 2- Standard Electrotherapy in people with Non-specific Neck Pain and Neck Pain, run by Uskudar University at 1 site in Turkey (Türkiye).
Trial 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. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Non-specific Neck Pain, Neck Pain
- What is being tested?
- Arm 1-Muscle Energy Technique (MET) and Arm 2- Standard Electrotherapy
- Type of treatment
- Medical device, Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Jan 2026to 15 Jul 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Turkey (Türkiye)1 site, 1 recruiting
- Recruiting
Avicenna International Hospital
Istanbul, Ataşehir, 34750
Deniz Demirci, PhD, 0090 533 240 86 61, deniz.demirci@uskudar.edu.tr
About this study
Official title: The Effect of Muscle Energy Technique on Neck Disability and Cervical Range of Motion in Patients With Non-Specific Neck Pain
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.
Read the 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.
- Conditions
- Non-specific Neck Pain, Neck Pain
- Being tested
- Arm 1-Muscle Energy Technique (MET), Arm 2- Standard Electrotherapy
- Keywords
- Neck Pain, Non-Specific Neck Pain, Muscle Energy Technique, Cervical Range of Motion, Neck Disability
- Medical subject headings
- Neck Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Arm 1-Muscle Energy Technique (MET)Behavioural
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 ElectrotherapyDevice
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 group | Role | What they receive |
|---|---|---|
| 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. Receives: 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. Receives: Device: Arm 2- Standard Electrotherapy |
What is being measured
The primary outcome is the main question the study is designed to answer.
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)
Measured: Baseline and at the end of the 10-day treatment period
Secondary outcomes (1)
Cervical Range of Motion
Cervical range of motion (ROM) will be measured using a goniometer or inclinometer. rotation movements will be evaluated to determine the functional mobility of the cervical spine. Cervical Range of Motion (degrees; higher values indicate better mobility)
Measured: Baseline and at the end of the 10-day treatment period
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Apr 2026
- Study start1 Jan 2026
- Primary completion30 Jun 2026 (estimated)
- Study completion15 Jul 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Non-specific Neck PainStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- 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.
- Masking
- None (open label)
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Uskudar University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Prof. Dr. Deniz Demirci, Uskudar University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07524075
- Sponsor's protocol ID
- USKU-2026-TCT-01
- Acronym
- MET-NP
- Status last verified
- Apr 2026
- First submitted
- 2 Apr 2026
- Last updated
- 13 Apr 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Individual participant data will not be shared due to privacy and ethical considerations.
Study at a glance
From the registry record, last updated by the sponsor on 13 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Muscle Energy Technique on Neck Disability and Cervical Range of Motion in Patients With Non-Specific Neck Pain
- ClinicalTrials.gov ID
- NCT07524075
- Acronym / sponsor ID
- MET-NP / USKU-2026-TCT-01
- Conditions
- Non-specific Neck Pain, Neck Pain
- Keywords
- Neck Pain, Non-Specific Neck Pain, Muscle Energy Technique, Cervical Range of Motion, Neck Disability
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Uskudar UniversityUniversity, hospital or other
- Study start
- 1 Jan 2026 (actual)
- Primary completion
- 30 Jun 2026 (estimated)
- Study completion
- 15 Jul 2026 (estimated)
- First posted
- 13 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- 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.
| Arm | Type | Receives |
|---|---|---|
| Muscle Energy Technique Group | Experimental | Behavioral: Arm 1-Muscle Energy Technique (MET)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. |
| Control Group | Active comparator | Device: Arm 2- Standard ElectrotherapyParticipants 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. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- 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
Key exclusion criteria (1 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| 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. | Behavioural | Muscle Energy Technique Group |
| Arm 2- Standard ElectrotherapyArm 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. | Device | Control Group |
Primary outcome
Neck Disability Index
Time frame: Baseline and at the end of the 10-day treatment period
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)
1 secondary outcome
Cervical Range of Motion
Time frame: Baseline and at the end of the 10-day treatment period
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Apr 2026.
- Individual participant dataSharing planned: No. Individual participant data will not be shared due to privacy and ethical considerations.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Arm 1-Muscle Energy Technique (MET) and Arm 2- Standard Electrotherapy in people with Non-specific Neck Pain and Neck Pain, run by Uskudar University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 13 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Deniz Demirci, PhD (0090 533 240 86 61, deniz.demirci@uskudar.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Neck Disability Index (time frame: Baseline and at the end of the 10-day treatment period). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Apr 2026.