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Shoulder PainNCT06890000

Effectiveness of Scapular Exercises Compared To Conventional Treatment in Shoulder Pain

A study testing Scapular Exercise in people with Shoulder Pain and Scapular Dyskinesis, run by Ankara Yildirim Beyazıt University at 1 site in Turkey (Türkiye).

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Shoulder Pain, Scapular Dyskinesis
What is being tested?
Scapular Exercise
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
48 participants
Where
1 siteTurkey (Türkiye)
Study dates
24 Mar 2025to 20 Oct 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Mehmet DELEN, PhD contact

+905548258720

mehmetdelen@aybu.edu.tr

Turkey (Türkiye)1 site, 1 recruiting
  • Universtiy of Health Sciences - Gülhane Faculty of Physiotherapy and Rehabilitation

    Ankara, 06010

    Mehmet Delen, PhD, +905548258720, mehmetdelen@yabu.edu.tr

    Mehmet DELEN, PhD

    Recruiting

Other trials in Turkey (Türkiye)

About this study

Official title: Effectiveness of Scapular Exercises Compared To Conventional Treatment in People With Shoulder Pain: A Randomized Controlled Study

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.

Being tested
Scapular Exercise, Control (Standard treatment)
Keywords
Shoulder pain, obvious scapular dyskinesis, Conventional Treatment, Scapular Exercises, Effectiveness
Medical subject headings
Shoulder Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Scapular ExerciseOther

    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.

  • Control (Standard treatment)Other

    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.

Study groups in NCT06890000
Study groupRoleWhat they receive
Scapular ExercisesExperimentalScapular exercise includes scapular clock exercise, rowing exercise, resisted external rotation, resisted punching exercise. The group program also includes conventional treatment.
Receives: Other: Scapular Exercise; Other: Control (Standard treatment)
Conventional TreatmentActive comparatorConventional treatment includes TENS, hotpack, Stretching exercises (posterior capsule and pectoral muscle), resisted flexion and abduction exercises
Receives: Other: Control (Standard treatment)

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

    Measured: Baseline and at 6 week

Secondary outcomes (1)
  1. Global Rate of Change

    GRoC is a reliable assessment method with 11 levels, frequently used to track changes in a participant's condition. Participants who selected the top two categories (much better and very much better) were considered recovered.

    Measured: Baseline and at 6 week

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Mar 2025
  2. Study start24 Mar 2025
  3. Primary completion1 Mar 2026 (estimated)
  4. Study completion20 Oct 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
48 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06890000
Sponsor's protocol ID
09/972
Status last verified
Mar 2025
First submitted
17 Mar 2025
Last updated
26 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Data will not be shared due to data protection rules

Publications

  • 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.

    PubMed 27422595

Questions about this trial

What is this clinical trial studying?

A study testing Scapular Exercise in people with Shoulder Pain and Scapular Dyskinesis, run by Ankara Yildirim Beyazıt University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 26 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Mehmet DELEN, PhD (+905548258720, mehmetdelen@aybu.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

shoulder pain and disability index (SPADI) (time frame: Baseline and at 6 week). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06890000, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Mar 2025.

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