← Back to Clinical Trials
Recruiting NCT06890000

NCT06890000 Effectiveness of Scapular Exercises Compared To Conventional Treatment in Shoulder Pain

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06890000
Status Recruiting
Phase
Sponsor Ankara Yildirim Beyazıt University
Condition Shoulder Pain
Study Type INTERVENTIONAL
Enrollment 48 participants
Start Date 2025-03-24
Primary Completion 2026-03-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Scapular ExerciseControl (Standard treatment)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 48 participants in total. It began in 2025-03-24 with a primary completion date of 2026-03-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

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.

Eligibility Criteria

Inclusion Criteria: * 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 Exclusion Criteria: * 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 & Investigator

Central Contact

Mehmet DELEN, PhD

✉ mehmetdelen@aybu.edu.tr

📞 +905548258720

Frequently Asked Questions

Who can join the NCT06890000 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Shoulder Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06890000 currently recruiting?

Yes, NCT06890000 is actively recruiting participants. Contact the research team at mehmetdelen@aybu.edu.tr for enrollment information.

Where is the NCT06890000 trial being conducted?

This trial is being conducted at Ankara, Turkey (Türkiye).

Who is sponsoring the NCT06890000 clinical trial?

NCT06890000 is sponsored by Ankara Yildirim Beyazıt University. The trial plans to enroll 48 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology