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Acute Effects of Percussion Massage in Nonspecific Neck Pain

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07307014
Enrollment
30
Registered
2025-12-29
Start date
2024-05-01
Completion date
2024-09-20
Last updated
2025-12-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain Musculoskeletal

Keywords

nonspesific neck pain, percussive massage, musculoskeletal disorders

Brief 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.

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.

Interventions

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.

DEVICESham Percussion Therapy

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.

Sponsors

Bezmialem Vakif University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Cervical Range of Motion (ROM)Immediately before and immediately after the interventionCervical 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.

Secondary

MeasureTime frameDescription
Pressure Pain Threshold (PPT)Immediately before and immediately after the interventionPressure 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026