Scapular Repositioning for Neck Pain and Scapular Dysfunction
Effects of Scapular Repositioning on Pain, Range of Motion, Proprioception, and Pressure Pain Threshold in Patients With Neck Pain and Scapular Dysfunction
1 other identifier
interventional
78
1 country
1
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.Does scapular repositioning reduce neck pain, increase range of motion, and improve joint position sense and pressure pain threshold?
- 2.Which type of scapular repositioning technique is more effective?
- 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.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.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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Apr 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 20, 2025
CompletedFirst Submitted
Initial submission to the registry
June 27, 2025
CompletedFirst Posted
Study publicly available on registry
July 24, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 19, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 19, 2025
CompletedMarch 31, 2026
March 1, 2026
8 months
June 27, 2025
March 30, 2026
Conditions
Keywords
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
EXPERIMENTALSelf-active scapular repositioning exercise
Passive scapular repositioning
EXPERIMENTALTherapist-assisted scapular repositioning
Sham scapular repositioning
SHAM COMPARATORSham scapular repositioning procedure
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.
The examiner will passively position and hold the participant's scapula in a neutral position.
The examiner will perform gentle shoulder girdle movements that do not alter scapular positioning.
Eligibility Criteria
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
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
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
- 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