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Clinical Trials in Turkey / NCT06875895
Recruiting Not applicable

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

NCT06875895 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-01-16
Last updated
2026-04-23

Condition(s) studied

Rotator Cuff Tears

Investigational drug(s) / intervention(s)

Traditional PhysiotherapyMotor Imagery Training

Traditional Physiotherapy: Hotpack, Tens and Ultrasound application

Motor Imagery Training: Kinesthetic and visual motor imagery will be applied.

Study 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

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
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).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kütahya Health Sciences University Kütahya Turkey (Türkiye) Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06875895 on ClinicalTrials.gov ↗ ← All trials in Turkey