NCT06875895

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2025

Geographic Reach
1 country

1 active site

Status
recruiting

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

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

March 9, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

March 13, 2025

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 3, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

May 3, 2026

Completed
Last Updated

April 23, 2026

Status Verified

April 1, 2026

Enrollment Period

1.2 years

First QC Date

March 9, 2025

Last Update Submit

April 20, 2026

Conditions

Keywords

Rotator CuffExercise therapyImagery

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 COMPARATOR

Traditional 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.

Other: Traditional Physiotherapy

Motor Imagery Training

EXPERIMENTAL

In 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.

Other: Motor Imagery Training

Interventions

Hotpack, Tens and Ultrasound application

Control Group (Traditional Physiotherapy)

Kinesthetic and visual motor imagery will be applied.

Motor Imagery Training

Eligibility Criteria

Age18 Years - 65 Years
Sexall(Gender-based eligibility)
Gender Eligibility DetailsRandomization was done according to gender, 40 female and 40 male.
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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)

RECRUITING

MeSH Terms

Conditions

Rotator Cuff Injuries

Condition Hierarchy (Ancestors)

RuptureWounds and InjuriesShoulder InjuriesTendon Injuries

Central Study Contacts

Sevtap CAKIR, Asst. Prof.

CONTACT

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
Model Details: A single-center randomized controlled study was designed.
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

Locations