NCT07307014

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 12, 2024

Completed
8 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 20, 2024

Completed
1.2 years until next milestone

First Submitted

Initial submission to the registry

December 13, 2025

Completed
16 days until next milestone

First Posted

Study publicly available on registry

December 29, 2025

Completed
Last Updated

December 29, 2025

Status Verified

December 1, 2025

Enrollment Period

4 months

First QC Date

December 13, 2025

Last Update Submit

December 13, 2025

Conditions

Keywords

nonspesific neck painpercussive massagemusculoskeletal disorders

Outcome Measures

Primary Outcomes (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.

    Immediately before and immediately after the intervention

Secondary Outcomes (1)

  • Pressure Pain Threshold (PPT)

    Immediately before and immediately after the intervention

Study Arms (2)

Percussion Massage Therapy

EXPERIMENTAL

Participants in this group receive a single session of percussion massage therapy applied to the bilateral upper trapezius muscles.

Device: Percussion Massage Therapy

Sham Percussion Therapy

SHAM COMPARATOR

Participants in this group receive a sham percussion intervention designed to mimic the active treatment without providing mechanical tissue stimulation.

Device: Sham Percussion Therapy

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.

Percussion Massage 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.

Sham Percussion Therapy

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bezmialem Vakif University

Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Musculoskeletal Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Asst.Prof

Study Record Dates

First Submitted

December 13, 2025

First Posted

December 29, 2025

Study Start

May 1, 2024

Primary Completion

September 12, 2024

Study Completion

September 20, 2024

Last Updated

December 29, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

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

Locations