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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorKutahya Health Sciences University

About this trial

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

This trial does not accept healthy volunteers

Qualifiers

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)

Disqualifiers

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).

Trial design

Design model

Parallel

Treatments tested in this trial

  • Traditional Physiotherapy

    Other intervention

    Hotpack, Tens and Ultrasound application

  • Motor Imagery Training

    Other intervention

    Kinesthetic and visual motor imagery will be applied.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Control Group (Traditional Physiotherapy)Active comparator 1 intervention
Group B: Motor Imagery TrainingExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
a day before the rehabilitation
2

Numerical Rating Scale

Pain intensity will be measured using the Numerical Rating Scale. A decrease in the point indicates that the pain is decreasing.

Time frame
a day before the rehabilitation
3

Numerical Rating Scale

Pain intensity will be measured using the Numerical Rating Scale. A decrease in the point indicates that the pain is decreasing.

Time frame
up to 4 weeks
4

Numerical Rating Scale

Pain intensity will be measured using the Numerical Rating Scale. A decrease in the point indicates that the pain is decreasing.

Time frame
up to 8 weeks

Secondary outcomes

1

Movement Imagery Questionnaire (MIQ-R)

This is an 8-item self-report questionnaire in which participants rate the vividness of their mental representations using a 7-point scale (1 = very difficult to see/feel and 7 = very easy to see/feel). This test will be used to ensure that the sample does not include individuals with extremely high or low motor imagery ability

Time frame
a day before the rehabilitation
2

Movement Imagery Questionnaire (MIQ-R)

This is an 8-item self-report questionnaire in which participants rate the vividness of their mental representations using a 7-point scale (1 = very difficult to see/feel and 7 = very easy to see/feel). This test will be used to ensure that the sample does not include individuals with extremely high or low motor imagery ability

Time frame
up to 4 weeks
3

Movement Imagery Questionnaire (MIQ-R)

This is an 8-item self-report questionnaire in which participants rate the vividness of their mental representations using a 7-point scale (1 = very difficult to see/feel and 7 = very easy to see/feel). This test will be used to ensure that the sample does not include individuals with extremely high or low motor imagery ability

Time frame
up to 8 weeks

Other outcomes

Sponsors and contacts

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