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Recruiting NCT06875895

NCT06875895 Effect of Motor Imagery Training on Pain, Functionality, Proprioception and Kinesiophobia in Partial Rotator Cuff Tear

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Clinical Trial Summary
NCT ID NCT06875895
Status Recruiting
Phase —
Sponsor Kutahya Health Sciences University
Condition Rotator Cuff Tears
Study Type INTERVENTIONAL
Enrollment 80 participants
Start Date 2025-01-16
Primary Completion 2026-04-03

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Traditional PhysiotherapyMotor Imagery Training

Eligibility Fast-Check

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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 80 participants in total. It began in 2025-01-16 with a primary completion date of 2026-04-03.

⚠ 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 aim of this study is to investigate the effects of motor imagery training on pain, functionality, proprioception and kinesiophobia in patients with partial rotator cuff tears. Participants will be randomly assigned to traditional physiotherapy and motor imagery groups. Interventions will be performed with a physiotherapist for a total of 20 sessions for 4 weeks, 5 days a week. The intervention program will be determined by the Specialist Physical Therapy Physician. Data will be collected before the study, at the end of the training in the 4th week and at the 8th week (follow-up evaluation). Motor imagery ability will be assessed with the Movement Imagery Questionnaire (MIQ-R), pain will be assessed with the Numerical Assessment Scale for functionality with the DASH, proprioception will be assessed with the inclinometer and kinesiophobia will be assessed with the Tampa Kinesiophobia Scale.

Eligibility Criteria

Inclusion Criteria: * Partial rotator cuff tear diagnosis. * Between the ages of 18-65 * Patients experiencing pain for at least 4 weeks. * Having a valid score on the Mini Mental Test (\>24) * Those without a history of any neurological or serious psychological illness. * Those who have not participated in a previous study on motor imagery training Exclusion Criteria: * Complete rotator cuff tear or conditions requiring surgical intervention, * Participants who have received treatment with corticosteroids by any means in the previous 6 months, * Participants who have a rotator cuff tear due to acute traumatic conditions (proximal humerus fracture).

Contact & Investigator

Central Contact

Sevtap CAKIR, Asst. Prof.

✉ sevtap.cakir@ksbu.edu.tr

📞 05343818927

Frequently Asked Questions

Who can join the NCT06875895 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Rotator Cuff Tears. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06875895 currently recruiting?

Yes, NCT06875895 is actively recruiting participants. Contact the research team at sevtap.cakir@ksbu.edu.tr for enrollment information.

Where is the NCT06875895 trial being conducted?

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

Who is sponsoring the NCT06875895 clinical trial?

NCT06875895 is sponsored by Kutahya Health Sciences University. The trial plans to enroll 80 participants.

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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: November 2026  ·  Data Methodology