Non-specific Neck PainNCT07150143
Effects of Connective Tissue Massage and Physical Modalities Combined With Stabilization Exercises in Chronic Neck Pain
A study testing Exercise, Connective tissue massage and Infrared therapy in people with Non-specific Neck Pain, run by Fenerbahce University at 1 site in Turkey (Türkiye).
Trial summary
This randomized, double-blinded controlled trial aims to investigate the comparative effects of connective tissue massage and physical modalities, when combined with cervical and scapulothoracic stabilization exercises, in individuals with chronic non-specific neck pain. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Non-specific Neck Pain
- What is being tested?
- Exercise, Connective tissue massage and Infrared therapy
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 27 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 12 Sep 2025to Oct 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
- Being between 18 and 65 years of age,
- Having non-specific chronic neck pain localized to the posterior cervical spine between the occipital region and the spinous process of the first thoracic vertebra,
- Being able to cooperate with the assessments to be performed in the study.
Who cannot join
- Neck pain resulting from trauma within the past 6 months;
- A history of surgery related to cervical problems;
- Clinical signs of cervical radiculopathy and/or myelopathy;
- Inflammatory arthritis involving the cervical spine;
- Tumors or infections of the cervical spine;
- Vertebrobasilar artery insufficiency;
Show all 9Show fewer
- Neurological disorders (such as multiple sclerosis, Parkinson's disease, or syringomyelia);
- Congenital anomalies affecting the spine; systemic diseases (such as diabetes mellitus);
- Shoulder pathologies (including tendinitis, bursitis, or capsulitis).
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
Fenerbahçe Üniversitesi
Ataşehir, Istanbul, 34734
Burcu AKKURT, Assistant Professor, 05536046713, burcu.akkurt@fbu.edu.tr
burcu.akkurt@fbu.edu.tr
About this study
Official title: Comparative Effects of Connective Tissue Massage and Physical Modalities Added to Cervical and Scapulothoracic Stabilization Exercises on Pain, Function, and Endurance in Individuals With Chronic Neck Pain
This randomized, double-blinded controlled trial aims to investigate the comparative effects of connective tissue massage and physical modalities, when combined with cervical and scapulothoracic stabilization exercises, in individuals with chronic non-specific neck pain. A total of 51 participants aged 18-65 years will be randomly assigned into three groups. Group 1 will perform stabilization exercises alone, Group 2 will receive stabilization exercises plus connective tissue massage, and Group 3 will receive stabilization exercises plus electrotherapy modalities (infrared, continuous ultrasound, and TENS). The interventions will be conducted twice weekly for 8 weeks, and participants will also perform home-based exercises daily. Primary outcomes include pain, disability, and endurance, while secondary outcomes focus on quality of life, cervical range of motion, and scapular function.
Read the detailed description
Chronic non-specific neck pain is a prevalent musculoskeletal disorder that adversely affects pain, functional capacity, and quality of life. Stabilization-based exercise programs are commonly recommended; however, the added benefits of connective tissue massage and physical modalities require further investigation.
This randomized, double-blinded controlled trial is designed to compare the effects of (1) stabilization exercises alone, (2) stabilization exercises combined with connective tissue massage, and (3) stabilization exercises combined with electrotherapy modalities (infrared therapy, continuous ultrasound, and TENS) on clinical outcomes in individuals with chronic non-specific neck pain.
A total of 51 participants between 18 and 65 years of age will be randomly allocated into three equal groups. All groups will receive supervised exercise sessions twice weekly for 8 weeks, each lasting 50 minutes (10 minutes of warm-up, 30 minutes of cervical and scapulothoracic stabilization, and 10 minutes of cool-down). Additionally, participants will be instructed to perform a one-hour home exercise program daily, supported with illustrated brochures.
The primary outcomes are:
- Pain (Bournemouth Neck Questionnaire)
- Disability (Neck Disability Index)
- Endurance (Deep Cervical Flexor Test)
The secondary outcomes are:
- Quality of life (WHOQOL-BREF)
- Cervical range of motion
- Scapular function (Lateral Scapular Slide Test and Scapular Dyskinesis Test)
By comparing these approaches, the study aims to determine whether the addition of connective tissue massage or physical modalities enhances the therapeutic effects of stabilization exercises on pain, function, and endurance in patients with chronic non-specific neck pain.
- Conditions
- Non-specific Neck Pain
- Being tested
- Exercise, Connective tissue massage, Infrared therapy, Continuous ultrasound, Conventional TENS
- Keywords
- non-specific neck pain, scapulothoracic stabilization exercises, connective tissue massage, electrotherapy
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ExerciseOther
Each exercise session lasts 50 minutes, consisting of a 10-minute warm-up, 30 minutes of stabilization exercises, and a 10-minute cool-down. Stabilization exercises are selected from an exercise pool according to the individual's needs, with progression ensuring throughout the program. The exercises will be administered face-to-face twice a week for eight weeks, and participants will be provided with illustrated brochures and instructed to perform a one-hour home exercise program daily.
Connective tissue massageOther
Connective tissue massage will be applied, starting from the basic regions and gradually incorporating other regions.
Infrared therapyOther
Infrared therapy will be applied for 20 minutes
Continuous ultrasoundOther
Continuous ultrasound will be applied to the right and left sides for 7 minutes each at an intensity of 2 W/cm².
Conventional TENSOther
20 minutes of conventional TENS will be administered to the painful area.
| Study group | Role | What they receive |
|---|---|---|
| Exercise | Active comparator | Each exercise session lasts 50 minutes, consisting of 10 minutes of warm-up, 30 minutes of stabilization exercises, and 10 minutes of cool-down. Stabilization exercises will be selected from an exercise pool according to the individual's needs, with progression ensured throughout the program. The exercises will be administered face-to-face twice a week for eight weeks, and participants will be provided with illustrated brochures and instructed to perform a one-hour home exercise program daily. Receives: Other: Exercise |
| Exercise, and Connective tissue massage | Experimental | Each exercise session lasts 50 minutes, consisting of 10 minutes of warm-up, 30 minutes of stabilization exercises, and 10 minutes of cool-down. Stabilization exercises will be selected from an exercise pool according to the individual's needs, with progression ensured throughout the program. The exercises will be administered face-to-face twice a week for eight weeks, and participants will be provided with illustrated brochures and instructed to perform a one-hour home exercise program daily. In this group, in addition to these exercises, connective tissue massage will be applied, starting from the basic regions and gradually incorporating other regions. Receives: Other: Exercise; Other: Connective tissue massage |
| Exercise, and Electro-physical modalities | Experimental | Each exercise session lasts 50 minutes, consisting of 10 minutes of warm-up, 30 minutes of stabilization exercises, and 10 minutes of cool-down. Stabilization exercises will be selected from an exercise pool according to the individual's needs, with progression ensured throughout the program. The exercises will be administered face-to-face twice a week for eight weeks, and participants will be provided with illustrated brochures and instructed to perform a one-hour home exercise program daily. Also, the electrotherapy program consists of 20 minutes of infrared therapy, continuous ultrasound will be applied to the right and left sides for 7 minutes each at an intensity of 2 W/cm², and 20 minutes of conventional TENS will be administered to the painful area. Receives: Other: Exercise; Other: Infrared therapy; Other: Continuous ultrasound; Other: Conventional TENS |
What is being measured
The primary outcome is the main question the study is designed to answer.
Neck Disability Index
To assess disability in neck pain, only the Neck Disability Index (NDI), which evaluates current pain and disability, was used. The NDI consists of 10 items grouped into 6 subdomains. Each item is scored on a scale from 0 to 5, with higher scores indicating greater levels of disability.
Measured: From enrollment to the end of treatment at 8 weeks
Deep Cervical Flexor Test
To evaluate deep neck flexor muscle endurance, the Deep Cervical Flexor Test was used. This test assesses the maximal contraction capacity of the deep cervical flexor muscles. It is performed in the supine position, with the participant lifting the head approximately 2.5 cm off the surface while maintaining chin retraction. The examiner places a hand under the participant's occiput. The test is terminated when cervical flexion is lost or the participant's head touches the examiner's hand, and the duration is recorded in seconds.
Measured: From enrollment to the end of treatment at 8 weeks.
Cervical Range of Motion Assessment
Cervical range of motion was assessed using a universal goniometer. The participant was seated in an upright position, and measurements were taken for cervical flexion, extension, right and left rotation, and right and left lateral flexion. For flexion and extension, the acromion was accepted as the pivot point, with the stationary arm held parallel to the ground and the movable arm aligned with the ear line. For rotation, a straight rod was placed between the participant's teeth, the midline of the head was accepted as the pivot point, the stationary arm was kept parallel to the ground, and the movable arm was aligned with the rod. For lateral flexion, the spinous process of C7 was accepted as the pivot point, the stationary arm was positioned parallel to the ground, and the movable arm was aligned with the spinous processes of the cervical vertebrae. Care was taken to ensure that the head was not rotated during the measurements.
Measured: From enrollment to the end of treatment at 8 weeks
Bournemouth Neck Questionnaire
For pain assessment, the Bournemouth Neck Questionnaire, which focuses on the participant's current symptoms over the past week, was used. The questionnaire evaluates aspects such as onset, localization, duration, type and characteristics of pain, aggravating and relieving factors, history of previous treatments, and accompanying symptoms. The Bournemouth Neck Questionnaire consists of 7 items, each scored on a scale from 0 to 10. The maximum score is 70, with higher scores indicating greater disability.
Measured: From enrollment to the end of treatment at 8 weeks.
Secondary outcomes (4)
Quality of Life Assessment
The World Health Organization Quality of Life Instrument, Short Form (WHOQOL-BREF) was used to assess the quality of life of the participants. The WHOQOL-BREF was developed by the World Health Organization and consists of six domains. Since each domain independently reflects the quality of life within its own scope, domain scores are calculated on a scale ranging from 4 to 20. Higher scores indicate better quality of life.
Measured: From enrollment to the end of treatment at 8 weeks.
Lateral Scapular Slide Test
The Lateral Scapular Slide Test (LSST) is a clinical assessment used to evaluate scapular positioning and detect scapular dyskinesis by measuring the distance between the inferior angle of the scapula and the spinous process at various arm positions.
Measured: From enrollment to the end of treatment at 8 weeks.
Scapular Dyskinesis Test
In the Scapular Dyskinesis Test, a load of 2.3 kg is used for individuals weighing 68.1 kg or more, and a load of 1.4 kg is used for those weighing less than 68.1 kg. Participants are instructed to hold the weights with the thumbs pointing upward, elbows extended, and shoulders in a neutral position, and to actively perform bilateral shoulder flexion and abduction. Each movement is repeated five times, during which scapular motion is observed. The presence of scapular winging or dysrhythmia during the movements is recorded as either "dyskinesis present" or "dyskinesis absent".
Measured: From enrollment to the end of treatment at 8 weeks.
Scapular Retraction Test
The Scapular Retraction Test is used to grade the strength of the supraspinatus muscle. The test begins with the traditional Empty Can Test, in which the patient's shoulder is placed in internal rotation, 90 degrees of flexion, and the scapular plane position ("scaption"). The examiner applies a downward force to the patient's arm while the patient resists. The test is then repeated with the examiner manually stabilizing the scapula in a retracted position. To achieve this, the examiner's fingers firmly grasp the patient's anterior shoulder over the clavicle, while the forearm is positioned along the medial border of the scapula. The test is considered positive if rotator cuff strength is restored, as indicated by the patient's improved ability to resist the examiner's downward force compared with the traditional Empty Can Test.
Measured: From enrollment to the end of treatment at 8 weeks.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Sep 2025
- Study start12 Sep 2025
- Primary completionNov 2025 (estimated)
- Study completionOct 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.
- More trials run by Fenerbahce UniversityThe sponsor's other registered studies.
- 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
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 27 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Fenerbahce University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Burcu AKKURT, Fenerbahce University
- Investigators
- Burcu AKKURT, PhD, Study director, Fenerbahçe University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07150143
- Sponsor's protocol ID
- 2015-KAEK-63-22-07
- Status last verified
- Sep 2025
- First submitted
- 24 Aug 2025
- Last updated
- 18 Sep 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 18 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparative Effects of Connective Tissue Massage and Physical Modalities Added to Cervical and Scapulothoracic Stabilization Exercises on Pain, Function, and Endurance in Individuals With Chronic Neck Pain
- ClinicalTrials.gov ID
- NCT07150143
- Acronym / sponsor ID
- 2015-KAEK-63-22-07
- Conditions
- Non-specific Neck Pain
- Keywords
- non-specific neck pain, scapulothoracic stabilization exercises, connective tissue massage, electrotherapy
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 27 participants (estimated)
- Lead sponsor
- Fenerbahce UniversityUniversity, hospital or other
- Study start
- 12 Sep 2025 (actual)
- Primary completion
- Nov 2025 (estimated)
- Study completion
- Oct 2026 (estimated)
- First posted
- 2 Sep 2025 (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 randomized, double-blinded controlled trial aims to investigate the comparative effects of connective tissue massage and physical modalities, when combined with cervical and scapulothoracic stabilization exercises, in individuals with chronic non-specific neck pain. A total of 51 participants aged 18-65 years will be randomly assigned into three groups. Group 1 will perform stabilization exercises alone, Group 2 will receive stabilization exercises plus connective tissue massage, and Group 3 will receive stabilization exercises plus electrotherapy modalities (infrared, continuous ultrasound, and TENS). The interventions will be conducted twice weekly for 8 weeks, and participants will also perform home-based exercises daily. Primary outcomes include pain, disability, and endurance, while secondary outcomes focus on quality of life, cervical range of motion, and scapular function.
Detailed description
Chronic non-specific neck pain is a prevalent musculoskeletal disorder that adversely affects pain, functional capacity, and quality of life. Stabilization-based exercise programs are commonly recommended; however, the added benefits of connective tissue massage and physical modalities require further investigation.
This randomized, double-blinded controlled trial is designed to compare the effects of (1) stabilization exercises alone, (2) stabilization exercises combined with connective tissue massage, and (3) stabilization exercises combined with electrotherapy modalities (infrared therapy, continuous ultrasound, and TENS) on clinical outcomes in individuals with chronic non-specific neck pain.
A total of 51 participants between 18 and 65 years of age will be randomly allocated into three equal groups. All groups will receive supervised exercise sessions twice weekly for 8 weeks, each lasting 50 minutes (10 minutes of warm-up, 30 minutes of cervical and scapulothoracic stabilization, and 10 minutes of cool-down). Additionally, participants will be instructed to perform a one-hour home exercise program daily, supported with illustrated brochures.
The primary outcomes are:
- Pain (Bournemouth Neck Questionnaire)
- Disability (Neck Disability Index)
- Endurance (Deep Cervical Flexor Test)
The secondary outcomes are:
- Quality of life (WHOQOL-BREF)
- Cervical range of motion
- Scapular function (Lateral Scapular Slide Test and Scapular Dyskinesis Test)
By comparing these approaches, the study aims to determine whether the addition of connective tissue massage or physical modalities enhances the therapeutic effects of stabilization exercises on pain, function, and endurance in patients with chronic non-specific neck pain.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Exercise | Active comparator | Other: ExerciseEach exercise session lasts 50 minutes, consisting of 10 minutes of warm-up, 30 minutes of stabilization exercises, and 10 minutes of cool-down. Stabilization exercises will be selected from an exercise pool according to the individual's needs, with progression ensured throughout the program. The exercises will be administered face-to-face twice a week for eight weeks, and participants will be provided with illustrated brochures and instructed to perform a one-hour home exercise program daily. |
| Exercise, and Connective tissue massage | Experimental | Other: Exercise, Other: Connective tissue massageEach exercise session lasts 50 minutes, consisting of 10 minutes of warm-up, 30 minutes of stabilization exercises, and 10 minutes of cool-down. Stabilization exercises will be selected from an exercise pool according to the individual's needs, with progression ensured throughout the program. The exercises will be administered face-to-face twice a week for eight weeks, and participants will be provided with illustrated brochures and instructed to perform a one-hour home exercise program daily. In this group, in addition to these exercises, connective tissue massage will be applied, starting from the basic regions and gradually incorporating other regions. |
| Exercise, and Electro-physical modalities | Experimental | Other: Exercise, Other: Infrared therapy, Other: Continuous ultrasound, Other: Conventional TENSEach exercise session lasts 50 minutes, consisting of 10 minutes of warm-up, 30 minutes of stabilization exercises, and 10 minutes of cool-down. Stabilization exercises will be selected from an exercise pool according to the individual's needs, with progression ensured throughout the program. The exercises will be administered face-to-face twice a week for eight weeks, and participants will be provided with illustrated brochures and instructed to perform a one-hour home exercise program daily. Also, the electrotherapy program consists of 20 minutes of infrared therapy, continuous ultrasound will be applied to the right and left sides for 7 minutes each at an intensity of 2 W/cm², and 20 minutes of conventional TENS will be administered to the painful area. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Being between 18 and 65 years of age,
- Having non-specific chronic neck pain localized to the posterior cervical spine between the occipital region and the spinous process of the first thoracic vertebra,
- Being able to cooperate with the assessments to be performed in the study.
Key exclusion criteria (9 listed)
- Neck pain resulting from trauma within the past 6 months;
- A history of surgery related to cervical problems;
- Clinical signs of cervical radiculopathy and/or myelopathy;
- Inflammatory arthritis involving the cervical spine;
- Tumors or infections of the cervical spine;
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 |
|---|---|---|
| ExerciseEach exercise session lasts 50 minutes, consisting of a 10-minute warm-up, 30 minutes of stabilization exercises, and a 10-minute cool-down. Stabilization exercises are selected from an exercise pool according to the individual's needs, with progression ensuring throughout the program. The exercises will be administered face-to-face twice a week for eight weeks, and participants will be provided with illustrated brochures and instructed to perform a one-hour home exercise program daily. | Other | Exercise, Exercise, and Connective tissue massage, Exercise, and Electro-physical modalities |
| Connective tissue massageConnective tissue massage will be applied, starting from the basic regions and gradually incorporating other regions. | Other | Exercise, and Connective tissue massage |
| Infrared therapyInfrared therapy will be applied for 20 minutes | Other | Exercise, and Electro-physical modalities |
| Continuous ultrasoundContinuous ultrasound will be applied to the right and left sides for 7 minutes each at an intensity of 2 W/cm². | Other | Exercise, and Electro-physical modalities |
| Conventional TENS20 minutes of conventional TENS will be administered to the painful area. | Other | Exercise, and Electro-physical modalities |
Primary outcome
Neck Disability Index
Time frame: From enrollment to the end of treatment at 8 weeks
To assess disability in neck pain, only the Neck Disability Index (NDI), which evaluates current pain and disability, was used. The NDI consists of 10 items grouped into 6 subdomains. Each item is scored on a scale from 0 to 5, with higher scores indicating greater levels of disability.
Deep Cervical Flexor Test
Time frame: From enrollment to the end of treatment at 8 weeks.
To evaluate deep neck flexor muscle endurance, the Deep Cervical Flexor Test was used. This test assesses the maximal contraction capacity of the deep cervical flexor muscles. It is performed in the supine position, with the participant lifting the head approximately 2.5 cm off the surface while maintaining chin retraction. The examiner places a hand under the participant's occiput. The test is terminated when cervical flexion is lost or the participant's head touches the examiner's hand, and the duration is recorded in seconds.
Cervical Range of Motion Assessment
Time frame: From enrollment to the end of treatment at 8 weeks
Cervical range of motion was assessed using a universal goniometer. The participant was seated in an upright position, and measurements were taken for cervical flexion, extension, right and left rotation, and right and left lateral flexion. For flexion and extension, the acromion was accepted as the pivot point, with the stationary arm held parallel to the ground and the movable arm aligned with the ear line. For rotation, a straight rod was placed between the participant's teeth, the midline of the head was accepted as the pivot point, the stationary arm was kept parallel to the ground, and the movable arm was aligned with the rod. For lateral flexion, the spinous process of C7 was accepted as the pivot point, the stationary arm was positioned parallel to the ground, and the movable arm was aligned with the spinous processes of the cervical vertebrae. Care was taken to ensure that the head was not rotated during the measurements.
Bournemouth Neck Questionnaire
Time frame: From enrollment to the end of treatment at 8 weeks.
For pain assessment, the Bournemouth Neck Questionnaire, which focuses on the participant's current symptoms over the past week, was used. The questionnaire evaluates aspects such as onset, localization, duration, type and characteristics of pain, aggravating and relieving factors, history of previous treatments, and accompanying symptoms. The Bournemouth Neck Questionnaire consists of 7 items, each scored on a scale from 0 to 10. The maximum score is 70, with higher scores indicating greater disability.
4 secondary outcomes
Quality of Life Assessment
Time frame: From enrollment to the end of treatment at 8 weeks.
Lateral Scapular Slide Test
Time frame: From enrollment to the end of treatment at 8 weeks.
Scapular Dyskinesis Test
Time frame: From enrollment to the end of treatment at 8 weeks.
Scapular Retraction Test
Time frame: From enrollment to the end of treatment at 8 weeks.
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 18 Sep 2025.
Related trials for Non-specific Neck Pain
Not yet recruiting
Effects of Whole-Body Vibration and Cervical Stabilization With Core Stabilization in Young Adults With Non-Specific Low Back Pain
Nonspecific Low Back Pain
Active, not recruiting
Multimodal Manual Therapy vs. Maitland Mobilization for Chronic Non-Specific Neck Pain
Chronic Neck Pain
Not yet recruiting
Effects of Muscle Energy Technique With and Without Scapulothoracic Mobilization on Neck Pain in Students
Non Psecific Neck Pain
Not yet recruiting
Effects of Cervical SNAGs With and Without Thoracic Manipulation on Neck Pain and Disability in Smartphone Users
Non Specific Neck Pain
Not yet recruiting
Comparison of the Effectiveness of Motor Imagery Exercises and Suboccipital Myofascial Release Techniques in Nonspecific Chronic Neck Pain
Non-specific Chronic Neck Pain
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.
Burcu AKKURT, PhD study director
Fenerbahçe University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Exercise, Connective tissue massage and Infrared therapy in people with Non-specific Neck Pain, run by Fenerbahce 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 3 inclusion and 9 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 18 Sep 2025. 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 Burcu AKKURT, PhD (+905536046713, burcu.akkurt@fbu.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: From enrollment to the end of treatment at 8 weeks). The study lists 4 primary outcomes in all. 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 18 Sep 2025.