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Chronic Non-specific Neck PainNCT07564492

Whole-Body Vibration vs. Exercises for Chronic Neck Pain in Young Adults

A study testing Whole Body Vibration and Sensorimotor Training in people with Chronic Non-specific Neck Pain and Sensorimotor Function, run by Pamukkale University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Chronic neck pain is a prevalent issue among young adults, potentially impacting pain levels, range of motion, posture, balance, and daily functional activities. This study is designed to compare two distinct physical therapy interventions for young individuals diagnosed with chronic non-specific neck pain: Whole-Body… Read more about this study

Who is it for?
Ages 18 to 30 years
What is being tested?
Whole Body Vibration and Sensorimotor Training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
38 participants
Where
1 siteTurkey (Türkiye)
Study dates
30 May 2025to 20 Mar 2026
Phase
Interventional
Are there results?
None posted in the registry

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 30 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Diagnosis of non-specific neck pain,
  • Age of 18 years or older,
  • History of neck pain for at least 3 months,
  • Pain intensity score of 3.5 or higher on the Visual Analog Scale (VAS),
  • Functional disability score of 5 or higher on the Neck Disability Index (NDI),
  • Sufficient literacy to complete the assessment scales.

Who cannot join

  • Diagnosis of disc herniation or spinal stenosis,
  • History of spinal surgery or major trauma,
  • Systemic conditions such as rheumatoid arthritis or advanced arthrosis,
  • Neurological diseases or balance disorders,
  • Severe pain in other body parts or recent lower extremity injuries.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Pamukkale University, Faculty of Physiotherapy and Rehabilitation.

    Denizli, Denizli, 20160

Other trials in Turkey (Türkiye)

About this study

Official title: Comparison of Whole-Body Vibration Therapy and Sensorimotor Exercise on Pain, Sensorimotor Function, and Balance in Young Adults With Chronic Nonspecific Neck Pain: A Randomized Controlled Trial

Chronic neck pain is a prevalent issue among young adults, potentially impacting pain levels, range of motion, posture, balance, and daily functional activities. This study is designed to compare two distinct physical therapy interventions for young individuals diagnosed with chronic non-specific neck pain: Whole-Body Vibration (WBV), involving standing on a vibrating platform, and Sensorimotor Exercise (SME), which focuses on improving neck awareness, coordination, balance, and motor control.

The primary objective is to determine whether one of these therapeutic approaches is more effective than the other in enhancing neck-related sensorimotor function, reducing pain intensity, and improving overall functional capacity over a 4-week intervention period. The study population consists of male and female university students aged 18 to 30 years presenting with chronic neck pain. The investigators anticipate that while both intervention protocols may yield clinical benefits, the comparative results will demonstrate which method provides superior short-term improvements in pain management and cervical function.

Being tested
Whole Body Vibration, Sensorimotor Training

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Whole Body VibrationDevice

    Participants received Whole-Body Vibration (WBV) training 3 days a week for a total of 4 weeks, totaling 12 sessions. Each session consisted of 10 sets of vibration. Each set involved 30 seconds of vibration followed by a 30-second rest period. The training was performed on a Compex Winplate™ vibration platform at a frequency of 30 Hz and an amplitude of 4 mm. Participants performed the exercises barefoot while maintaining various positions, starting from a static semi-squat (15° mini-squat) and progressing to more dynamic and advanced balance tasks across three levels. Each session initially lasted 12-15 minutes and progressed to 20-25 minutes based on participant tolerance.

  • Sensorimotor TrainingProcedure or surgery

    Participants underwent a structured and progressive sensorimotor exercise program conducted 3 days a week for a total of 4 weeks. The protocol was tailored across three stages, with session durations increasing from an initial 12-15 minutes to 20 minutes. Key components included oculomotor and eye-head coordination tasks using a laser pointer for gaze stability, as well as static and dynamic balance exercises that progressed from wide to narrow bases of support and from stable to unstable surfaces. Additionally, the program incorporated deep neck flexor strengthening through precision-focused chin-tuck exercises using small exercise balls, and functional tasks such as squatting combined with laser pointer tracking. Exercises progressed from 5-7 repetitions to 10-12 repetitions per session based on individual tolerance, with 1-3 minute rest intervals provided between sets.

Study groups in NCT07564492
Study groupRoleWhat they receive
Whole Body VibrationExperimentalNot described
Receives: Device: Whole Body Vibration
Sensorimotor TrainingActive comparatorNot described
Receives: Procedure: Sensorimotor Training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Visual Analog Scale (VAS)

    Participants' pain perception was evaluated using the VAS, a tool widely utilized in clinical and scientific research that ranges from 0 to 10 points (0=no pain, 10=maximum pain). Pain intensity was categorized according to the classification described, using the VAS scoring system, which is a validated and reliable scale for measuring musculoskeletal pain.

    Measured: Baseline and at the end of treatment (4 weeks).

Secondary outcomes (8)
  1. Joint Position Sense Error (JPSE) test.

    For the evaluation of cervical Joint Position Sense (JPS), the CROM device was preferred as it is an effective, simple, and cost-efficient measurement tool, similar to its use in Range of Motion (ROM) assessment. This ensured consistency across the evaluation environment, preparation phase, standardized measurement posture, device placement, and calibration. The participants' cervical ROM in three planes was measured three times, and the arithmetic mean of these measurements served as the baseline for JPS assessment. The target angle for the JPS test was then calculated as 65% of the average ROM for the respective cervical movement.

    Measured: Baseline and at the end of treatment (4 weeks).

  2. Cervical Range of Motion (CROM) device.

    Active cervical flexion, extension, right-left rotation, and right-left lateral flexion were evaluated using the Baseline CROM Deluxe device. The CROM device consists of two gravity-dependent goniometers and a head-mounted compass dial, allowing for range of motion (ROM) measurements across three anatomical planes. During the assessments, participants were instructed to sit with their feet flat on the floor, hands resting on their thighs, and the pelvis in a neutral position. For active movements, they were asked to move the head at a constant speed while keeping the back and shoulders stationary, followed by a 5-10 second rest in the neutral position after each movement.

    Measured: Baseline and at the end of treatment (4 weeks).

  3. Gaze Stability Test

    To assess gaze stability, the Head-Eye Movement Control Test was conducted. For participant safety, the testing area was positioned in a corner of the room. A camera was mounted on a tripod at eye level at the center of a 1-meter equilateral triangle marked on the floor. Participants were seated in a neutral position and instructed to rotate their head as rapidly as possible to the right and left while maintaining visual fixation on the camera lens. Performance was scored using a 3-point scale:

    • 0 (negative): Stable gaze with smooth, well-coordinated, and rapid head movements.
    • 1 (mild positive): Stable gaze but with slightly uncontrolled head movements.
    • 2 (strong positive): Repeatedly unstable gaze with slow and uncontrolled head movements.

    Measured: Baseline and at the end of treatment (4 weeks)

  4. The Single-leg Stance Test

    Static balance was assessed using the Single-Leg Stance (SLS) test, performed separately for the right and left lower extremities under both eyes-open and eyes-closed conditions. Three trials were conducted for each condition, and the mean duration was recorded. The test was terminated if the weight-bearing foot shifted from its original position, the non-weight-bearing foot touched the floor, the participant sought external support, or the maximum duration of 60 seconds was reached.

    Measured: Baseline and at the end of treatment (4 weeks).

  5. Y-Balance Test (YBT).

    Dynamic postural was assessed using the Y-Balance Test (YBT). Reach distances were measured in three directions: anterior (ANT), posterolateral (PL), and posteromedial (PM). To allow for data normalization, participants' leg length was measured from the anterior superior iliac spine (ASIS) to the medial malleolus. Following six practice trials to minimize learning effects, the maximum reach of three successful trials in each direction was recorded and normalized to leg length to calculate a composite balance score.

    Measured: Baseline and at the end of treatment (4 weeks).

  6. head posture analysis.

    To evaluate the alignment of the cervical spine, participants' head posture was assessed by measuring the craniovertebral angle (CVA). The CVA is defined as the angle formed between the horizontal plane and a line connecting the midpoint of the tragus of the ear to the C7 spinous process. Measurements were conducted using the photogrammetry technique while participants were in a standing position. For this purpose, a digital camera was positioned at a fixed point 1.5 meters from the participant at shoulder level. After placing an anatomical marker on the C7 spinous process, participants were instructed to bring their heads into a neutral position through small flexion and extension movements and to look at a fixed point directly in front of them. CVA values were calculated from photographs taken from the left lateral projection. A decrease in the CVA value was recorded as an indicator of increased anterior head posture (forward head displacement).

    Measured: Baseline and at the end of treatment (4 weeks).

  7. Fremantle Neck Awareness Questionnaire (FreNAQ).

    Neck-specific body perception and awareness were evaluated using the Fremantle Neck Awareness Questionnaire (FreNAQ). This 9-item scale assesses body image, proprioception, and perceptual distortions of the neck region. Each item is scored on a 5-point Likert scale (0 = never, 4 = always), with higher total scores indicating greater body image distortion. The Turkish version of the FreNAQ has been previously validated and demonstrated high reliability for individuals with neck pain.

    Measured: Baseline and at the end of treatment (4 weeks).

  8. Bournemouth Neck Pain Questionnaire(BNPQ).

    For a detailed evaluation of neck pain and its multidimensional impacts, the seven-item Bournemouth Neck Pain Questionnaire (BNPQ) was utilized to assess participants' pain intensity, as well as kinesiophobia, anxiety, depression, and coping abilities. This scale provides a biopsychosocial assessment by covering four of the five components of the International Classification of Functioning, Disability and Health (ICF), as it assesses pain intensity over the past week, disability in daily and social activities, levels of anxiety and depression, kinesiophobia, and pain control abilities. The BNPQ was selected for its ability to determine the comprehensive effects of neck pain, and its Turkish version has demonstrated validity and reliability (Cronbach's alpha = 0.865; ICC = 0.963).

    Measured: Baseline and at the end of treatment (4 weeks)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 May 2026
  2. Study start30 May 2025
  3. Primary completion20 Mar 2026
  4. Study completion20 Mar 2026

Resources

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
Single blind
Who is masked
Outcomes assessor
Enrolment
38 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07564492
Sponsor's protocol ID
E-60116787-020-664846
Status last verified
Oct 2026
First submitted
15 Apr 2026
Last updated
16 Oct 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Whole Body Vibration and Sensorimotor Training in people with Chronic Non-specific Neck Pain and Sensorimotor Function, run by Pamukkale 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 6 inclusion and 5 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: finished, as of the sponsor's last update on 16 Oct 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Visual Analog Scale (VAS) (time frame: Baseline and at the end of treatment (4 weeks).). 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 16 Oct 2026.

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