NCT06890000

Brief Summary

The contribution of the scapula to shoulder joint movement is great. The contribution of the scapula bone is more prominent, especially in overhead activities. Therefore, the position and movement of the scapula are generally examined in people with shoulder disease. Scapula-focused exercises are used in patients with shoulder problems. However, some studies focused on the effectiveness of scapula-focused exercises on shoulder problems. Thes studies fundings are controversial. Scapular dyskinesis has not been evaluated in these studies. No study has set the condition of having scapular dyskinesis as an inclusion criterion. Scapular-focused exercises are expected to have a greater effect especially on patients with scapular dyskinesis. Therefore, the aim of this study is to examine the effectiveness of scapula-focused exercises on patients with shoulder pain and obvious scapular dyskinesis.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable

Timeline
5mo left

Started Mar 2025

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress71%
Mar 2025Oct 2026

First Submitted

Initial submission to the registry

March 17, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

March 21, 2025

Completed
3 days until next milestone

Study Start

First participant enrolled

March 24, 2025

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2026

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 20, 2026

Expected
Last Updated

March 26, 2025

Status Verified

March 1, 2025

Enrollment Period

11 months

First QC Date

March 17, 2025

Last Update Submit

March 24, 2025

Conditions

Keywords

Shoulder painobvious scapular dyskinesisConventional TreatmentScapular ExercisesEffectiveness

Outcome Measures

Primary Outcomes (1)

  • shoulder pain and disability index (SPADI)

    SPADI is a self reported outcome for shoulder disorders. SPADI includes 13 questions. Scores range from 0 to 100. The higher a patient scores on the SPADI, the greater the level of pain/disability.

    Baseline and at 6 week

Secondary Outcomes (1)

  • Global Rate of Change

    Baseline and at 6 week

Study Arms (2)

Scapular Exercises

EXPERIMENTAL

Scapular exercise includes scapular clock exercise, rowing exercise, resisted external rotation, resisted punching exercise. The group program also includes conventional treatment.

Other: Scapular ExerciseOther: Control (Standard treatment)

Conventional Treatment

ACTIVE COMPARATOR

Conventional treatment includes TENS, hotpack, Stretching exercises (posterior capsule and pectoral muscle), resisted flexion and abduction exercises

Other: Control (Standard treatment)

Interventions

Scapular exercise includes scapular clock exercise (3 sets of 10 repetitions), rowing exercise (3 sets of 10 repetitions), resisted external rotation (3 sets of 10 repetitions), resisted punching exercise (3 sets of 10 repetitions). The rowing, external rotation and punching exercises will do with theraband. When participants complete the elastic band exercises easily and do not report any muscle fatigue, they will move on to the next level of difficulty. The color order of the bands is yellow, red, green and blue. The exercises will begin with the yellow elastic band, which provides the least resistance. The intervention will last for 6 weeks, with 2 training sessions per week and each training session lasting 15-20 minutes.

Scapular Exercises

Conventional Treatment includes TENS (100 Hz) with hotpack (20 minutes), Stretching exercises (posterior capsule and pectoral muscle), resisted flexion and abduction exercises. The rowing, external rotation and punching exercises will do with theraband. When participants complete the elastic band exercises easily and do not report any muscle fatigue, they will move on to the next level of difficulty. The color order of the bands is yellow, red, green and blue. The exercises will begin with the yellow elastic band, which provides the least resistance. The intervention will last for 6 weeks, with 2 training sessions per week and each training session lasting 30-45 minutes.

Conventional TreatmentScapular Exercises

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Having shoulder pain for at least 1 month
  • Having obvious scapular dyskinesia
  • Having a shoulder ROM (range of motion) at least 120º
  • Being 18 years of age or older

You may not qualify if:

  • Having received any shoulder treatment in the last 6 months
  • Having an acromioclavicular joint problem
  • Having a diagnosis of frozen shoulder
  • Having a fracture in the shoulder area
  • Having a major rotator cuff muscle tear
  • Having a diagnosis of calcific rotator cuff tendinopathy
  • Having a neurological or rheumatological disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Universtiy of Health Sciences - Gülhane Faculty of Physiotherapy and Rehabilitation

Ankara, 06010, Turkey (Türkiye)

RECRUITING

Related Publications (1)

  • Bury J, West M, Chamorro-Moriana G, Littlewood C. Effectiveness of scapula-focused approaches in patients with rotator cuff related shoulder pain: A systematic review and meta-analysis. Man Ther. 2016 Sep;25:35-42. doi: 10.1016/j.math.2016.05.337. Epub 2016 Jun 4.

    PMID: 27422595BACKGROUND

MeSH Terms

Conditions

Shoulder Pain

Condition Hierarchy (Ancestors)

ArthralgiaJoint DiseasesMusculoskeletal DiseasesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Mehmet DELEN, PhD

CONTACT

Study Design

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

Study Record Dates

First Submitted

March 17, 2025

First Posted

March 21, 2025

Study Start

March 24, 2025

Primary Completion

March 1, 2026

Study Completion (Estimated)

October 20, 2026

Last Updated

March 26, 2025

Record last verified: 2025-03

Data Sharing

IPD Sharing
Will not share

Data will not be shared due to data protection rules

Locations