Effect of Motor Imagery Training on Pain, Functionality, Proprioception and Kinesiophobia in Partial Rotator Cuff Tear
1 other identifier
interventional
80
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 16, 2025
CompletedFirst Submitted
Initial submission to the registry
March 9, 2025
CompletedFirst Posted
Study publicly available on registry
March 13, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 3, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 3, 2026
CompletedApril 23, 2026
April 1, 2026
1.2 years
March 9, 2025
April 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (10)
Standardized Mini Mental Test
The Standardized Mini Mental Test is a short, efficient and standard method that can be preferred in determining the cognitive level of the individual. It is collected under five headings: orientation, recording memory, attention and calculation, recall and language. There are eleven items that individuals will answer. It is evaluated out of a total of 30 points. The threshold value was determined as 24 points in the Turkish validity and reliability study.
a day before the rehabilitation
Numerical Rating Scale
Pain intensity will be measured using the Numerical Rating Scale. A decrease in the point indicates that the pain is decreasing.
a day before the rehabilitation
Numerical Rating Scale
Pain intensity will be measured using the Numerical Rating Scale. A decrease in the point indicates that the pain is decreasing.
up to 4 weeks
Numerical Rating Scale
Pain intensity will be measured using the Numerical Rating Scale. A decrease in the point indicates that the pain is decreasing.
up to 8 weeks
Disabilities of the arm, shoulder, and hand
Disabilities of the arm, shoulder, and hand scale is a questionnaire developed to assess the musculoskeletal pathology of the upper extremity and the entire upper extremity in general. It consists of 30 questions that evaluate the degree of difficulty in performing different activities using the upper extremity in daily life in the last week (21 questions), symptoms consisting of pain, activity-related pain, numbness, joint stiffness and weakness (5 questions), and the effects of pathologies on social life, sleep, work and psychological status (4 questions). All questions have a 5-point Likert model (1: no difficulty, 2: mild difficulty, 3: moderate difficulty, 4: extreme difficulty, 5: completely unable to do). The Turkish version of the DASH Questionnaire was used.
a day before the rehabilitation
Disabilities of the arm, shoulder, and hand
Disabilities of the arm, shoulder, and hand scale is a questionnaire developed to assess the musculoskeletal pathology of the upper extremity and the entire upper extremity in general. It consists of 30 questions that evaluate the degree of difficulty in performing different activities using the upper extremity in daily life in the last week (21 questions), symptoms consisting of pain, activity-related pain, numbness, joint stiffness and weakness (5 questions), and the effects of pathologies on social life, sleep, work and psychological status (4 questions). All questions have a 5-point Likert model (1: no difficulty, 2: mild difficulty, 3: moderate difficulty, 4: extreme difficulty, 5: completely unable to do). The Turkish version of the DASH Questionnaire was used.
up to 4 weeks
Disabilities of the arm, shoulder, and hand
Disabilities of the arm, shoulder, and hand scale is a questionnaire developed to assess the musculoskeletal pathology of the upper extremity and the entire upper extremity in general. It consists of 30 questions that evaluate the degree of difficulty in performing different activities using the upper extremity in daily life in the last week (21 questions), symptoms consisting of pain, activity-related pain, numbness, joint stiffness and weakness (5 questions), and the effects of pathologies on social life, sleep, work and psychological status (4 questions). All questions have a 5-point Likert model (1: no difficulty, 2: mild difficulty, 3: moderate difficulty, 4: extreme difficulty, 5: completely unable to do). The Turkish version of the DASH Questionnaire was used.
up to 8 weeks
Tampa Kinesiophobia Scale
The Tampa Kinesiophobia Scale will be used. A 4-point Likert scale is used and the total score is 33. The higher a person's score on the scale, the greater their fear of movement.
a day before the rehabilitation
Tampa Kinesiophobia Scale
The Tampa Kinesiophobia Scale will be used. A 4-point Likert scale is used and the total score is 33. The higher a person's score on the scale, the greater their fear of movement.
up to 4 weeks
Tampa Kinesiophobia Scale
The Tampa Kinesiophobia Scale will be used. A 4-point Likert scale is used and the total score is 33. The higher a person's score on the scale, the greater their fear of movement.
up to 8 weeks
Secondary Outcomes (3)
Movement Imagery Questionnaire (MIQ-R)
a day before the rehabilitation
Movement Imagery Questionnaire (MIQ-R)
up to 4 weeks
Movement Imagery Questionnaire (MIQ-R)
up to 8 weeks
Study Arms (2)
Control Group (Traditional Physiotherapy)
ACTIVE COMPARATORTraditional physical therapy will begin with the application of Hotpack, Tens and Ultrasound to the painful area for five minutes. Then, stretching exercises will be performed at the pain limit for the six main shoulder movements in the shoulder joint. Then, wand exercises, pendulum exercises, isometric exercises for the shoulder joint and strengthening active exercises will be given in order to increase the normal range of motion in the shoulder joint. The six main shoulder movements will be actively performed (flexion, extension, abduction, adduction, medial and lateral rotations). After the 5th session, weights will be added according to the patient's condition.
Motor Imagery Training
EXPERIMENTALIn motor imagery training, exercises in traditional physiotherapy will be applied with kinesthetic and visual motor imagery. Each movement will be divided into five sets consisting of two trials separated by 10 repetitions and 30-second rest periods. It will also be emphasized through practice that the functional movement imagined and the times when this movement is actually actively performed should be similar. Individuals' eyes will be closed throughout the entire motor imagery training. At the very beginning of the session, a relaxation exercise lasting approximately 5 minutes will be performed in order to maximize attention during motor imagery. Whether or not individuals are performing imagery will be monitored by monitoring heart rate variables from autonomic functions. In order to ensure standardization during imagery, commands will be applied with audio recordings containing metaphors.
Interventions
Hotpack, Tens and Ultrasound application
Kinesthetic and visual motor imagery will be applied.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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 the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Kütahya Health Sciences University
Kütahya, 43000, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Sevtap CAKIR, Asst. Prof.
CONTACT
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Asst. Prof.
Study Record Dates
First Submitted
March 9, 2025
First Posted
March 13, 2025
Study Start
January 16, 2025
Primary Completion
April 3, 2026
Study Completion
May 3, 2026
Last Updated
April 23, 2026
Record last verified: 2026-04