NCT07083570

Brief Summary

This randomized controlled trial is designed to evaluate the effects of scapular repositioning in individuals with neck pain and scapular dysfunction. The main questions it aims to answer are:

  1. 1.Does scapular repositioning reduce neck pain, increase range of motion, and improve joint position sense and pressure pain threshold?
  2. 2.Which type of scapular repositioning technique is more effective?
  3. 3.Active scapular repositioning: The examiner will first passively position the scapula in a neutral position on the posterior chest wall. The participant will then be instructed to actively maintain that position for 10 seconds. This procedure will be repeated for 10 repetitions, with a 10-second rest interval between each repetition.
  4. 4.Passive scapular repositioning: The examiner will passively position and hold the scapula in a neutral position for 10 seconds. This procedure will be repeated for 10 repetitions, with a 10-second rest interval between each repetition.
  5. 5.Sham scapular repositioning (control): The examiner will perform gentle shoulder movements that do not alter scapular positioning. Each movement will be held for 10 seconds, repeated 10 times, with a 10-second rest interval between repetitions.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
78

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Apr 2025

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

April 20, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

June 27, 2025

Completed
27 days until next milestone

First Posted

Study publicly available on registry

July 24, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 19, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 19, 2025

Completed
Last Updated

March 31, 2026

Status Verified

March 1, 2026

Enrollment Period

8 months

First QC Date

June 27, 2025

Last Update Submit

March 30, 2026

Conditions

Keywords

Neck painScapular dysfunctionScapular repositioningExerciseIntervention

Outcome Measures

Primary Outcomes (4)

  • Neck pain intensity

    Neck pain intensity measured by the Visual Analog Scale (VAS; 0-100 mm, where higher scores indicate worse pain).

    Baseline, immediately after the intervention and at 30 minutes post-intervention

  • Cervical range of motion

    Cervical range of motion measured using a goniometer in flexion, extension, left and right lateral flexion, and left and right rotation (measured in degrees).

    Baseline, immediately after the intervention and at 30 minutes post-intervention

  • Cervical and shoulder proprioception

    Cervical joint position error (JPE) measured using a laser pointer mounted on a headband at the center of the head during blindfolded active extension and left/right rotation. Shoulder joint position error (JPE) measured using a laser pointer placed proximal to the lateral epicondyle during blindfolded active shoulder flexion and abduction. An absolute error between starting and return positions will be recorded in millimeters and converted to degrees. Higher values indicate greater impairment.

    Baseline, immediately after the intervention and at 30 minutes post-intervention

  • Pressure pain threshold at upper trapezius and levator scapulae muscles

    Pressure pain threshold (PPT) measured by algometer; values recorded in Newtons (N), with lower scores indicating greater pain sensitivity (worse outcome).

    Baseline, immediately after the intervention and at 30 minutes post-intervention

Study Arms (3)

Active scapular repositioning

EXPERIMENTAL

Self-active scapular repositioning exercise

Behavioral: Active scapular repositioning

Passive scapular repositioning

EXPERIMENTAL

Therapist-assisted scapular repositioning

Procedure: Passive scapular repositioning

Sham scapular repositioning

SHAM COMPARATOR

Sham scapular repositioning procedure

Procedure: Sham scapular repositioning

Interventions

The examiner will first passively position the participant's scapula in a neutral position on the posterior chest wall. The participant will then be instructed to actively maintain that position.

Active scapular repositioning

The examiner will passively position and hold the participant's scapula in a neutral position.

Passive scapular repositioning

The examiner will perform gentle shoulder girdle movements that do not alter scapular positioning.

Sham scapular repositioning

Eligibility Criteria

Age18 Years - 59 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Chronic idiopathic neck pain for ≥3 months
  • An average pain intensity over the past week ≥3 mm on a Visual Analogue Scale (VAS)
  • A current score of at least 10/100 on the Neck Disability Index-Thai version
  • Having altered scapular alignment ipsilateral to the more painful side of neck pain

You may not qualify if:

  • History of neck injury or surgery
  • History of shoulder girdle pain, fracture, surgery or dislocation
  • History of neurological conditions (e.g. stroke, Parkinson's disease, brachial plexus injury)
  • History of marked spinal abnormalities (e.g. kyphosis, scoliosis) and other musculoskeletal conditions that could affect the scapular movement (e.g. myofascial pain syndrome, fibromyalgia, inflammatory joint disease, and/or autoimmune diseases)
  • Have participated in any specific training of the neck or shoulder girdle muscles in the last 6 months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

School of Allied Health Sciences, University of Phayao

Phayao, Changwat Phayao, 56000, Thailand

Location

MeSH Terms

Conditions

Neck PainMotor Activity

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsBehavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: 1. Active scapular repositioning 2. Passive scapular repositioning 3. Sham scapular repositioning (control)
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

June 27, 2025

First Posted

July 24, 2025

Study Start

April 20, 2025

Primary Completion

December 19, 2025

Study Completion

December 19, 2025

Last Updated

March 31, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations