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Neck Pain MusculoskeletalNCT07307014

Acute Effects of Percussion Massage in Nonspecific Neck Pain

A study testing Percussion Massage Therapy in people with Neck Pain Musculoskeletal, run by Bezmialem Vakif 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

This randomized controlled trial aimed to investigate the acute effects of percussion massage therapy compared with a sham intervention on cervical range of motion and pressure pain threshold in individuals with nonspecific neck pain. Read more about this study

Who is it for?
Ages 18 to 60 years
Conditions the study is for
Neck Pain Musculoskeletal
What is being tested?
Percussion Massage Therapy
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
30 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 May 2024to 20 Sep 2024
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 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Adults aged 18 to 60 years
  • Diagnosis of nonspecific neck pain
  • Resting neck pain intensity of ≥3 on the Visual Analog Scale (VAS)
  • Willingness to participate and provide written informed consent

Who cannot join

  • History of cervical spine fracture, tumor, or inflammatory disease
  • Previous surgery involving the neck or shoulder region
  • Neurological deficits related to the cervical spine
  • Pregnancy or suspected pregnancy
  • Cognitive impairment or inability to understand study procedures

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Bezmialem Vakif University

    Istanbul

Other trials in Turkey (Türkiye)

About this study

Official title: Quick Relief or Real Response? Acute Effects of Percussion Massage Versus Sham Treatment in Individuals With Nonspecific Neck Pain: A Randomized Controlled Trial

This randomized controlled trial aimed to investigate the acute effects of percussion massage therapy compared with a sham intervention on cervical range of motion and pressure pain threshold in individuals with nonspecific neck pain.

Read the detailed description

Nonspecific neck pain is a common musculoskeletal condition associated with reduced cervical mobility and increased pain sensitivity. Percussion massage therapy has gained popularity as a therapeutic modality; however, evidence regarding its true physiological effects remains limited.

This single-blind randomized controlled trial investigated the immediate effects of percussion massage therapy compared with a sham intervention in individuals with nonspecific neck pain. Participants were randomly allocated to either a percussion massage therapy group or a sham percussion therapy group. Cervical range of motion and pressure pain threshold were assessed before and immediately after the intervention.

Being tested
Percussion Massage Therapy, Sham Percussion Therapy
Keywords
nonspesific neck pain, percussive massage, musculoskeletal disorders
Medical subject headings
Musculoskeletal Diseases

What participants receive

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

  • Percussion Massage TherapyDevice

    Percussion massage therapy is applied using a handheld percussive massage device. The intervention is performed with the participant in a seated position and targets the bilateral upper trapezius muscles for a total duration of 6 minutes. A circular massage head is used to deliver percussive stimulation along the muscle for 2 minutes on each side, followed by focused stimulation at two trigger points using a bullet head attachment for 30 seconds per point at a frequency of 30 Hz.

  • Sham Percussion TherapyDevice

    The same percussive massage device is activated to produce comparable sound and vibration cues but is held at a fixed distance from the skin without physical contact. The duration of the procedure and therapist-participant interaction are matched to the experimental intervention to maintain participant blinding.

Study groups in NCT07307014
Study groupRoleWhat they receive
Percussion Massage TherapyExperimentalParticipants in this group receive a single session of percussion massage therapy applied to the bilateral upper trapezius muscles.
Receives: Device: Percussion Massage Therapy
Sham Percussion TherapySham comparatorParticipants in this group receive a sham percussion intervention designed to mimic the active treatment without providing mechanical tissue stimulation.
Receives: Device: Sham Percussion Therapy

What is being measured

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

  1. Cervical Range of Motion (ROM)

    Cervical range of motion (ROM) is assessed in flexion, extension, right and left lateral flexion, and right and left rotation using a digital goniometer. Measurements are performed in a seated position by a blinded assessor following standardized procedures.

    Measured: Immediately before and immediately after the intervention

Secondary outcomes (1)
  1. Pressure Pain Threshold (PPT)

    Pressure pain threshold (PPT) is measured bilaterally at two standardized points over the upper trapezius muscle using a digital pressure algometer. Pressure is gradually increased until the participant first perceives pain, and the mean of three measurements at each site is recorded.

    Measured: Immediately before and immediately after the intervention

Timeline

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

  1. First posted29 Dec 2025
  2. Study start1 May 2024
  3. Primary completion12 Sep 2024
  4. Study completion20 Sep 2024

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
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07307014
Sponsor's protocol ID
BVUçes
Status last verified
Dec 2025
First submitted
13 Dec 2025
Last updated
29 Dec 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Data supporting the findings of this study are available from the corresponding author upon reasonable request. Owing to ethical and privacy considerations, the data were not publicly available

Questions about this trial

What is this clinical trial studying?

A study testing Percussion Massage Therapy in people with Neck Pain Musculoskeletal, run by Bezmialem Vakif 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 4 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 29 Dec 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. Some participants in this study may receive a placebo. 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?

Cervical Range of Motion (ROM) (time frame: Immediately before and immediately after the intervention). 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 29 Dec 2025; AzTrials last refreshed its copy on 8 Nov 2026.

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