Shoulder Pain Clinical Trial
Official title:
Does Motor Imagination Have a Therapeutic Role in Arthroscopic Rotator Cuff Repair? Randomized Controlled, Single-Blind Trial
Objective: The aim of this study is to investigate the effect of motor imagery on muscle activity, pain, and function in arthroscopic rotator cuff repair. Methods: As a result of the power analysis (G-Power), 36 participants are planned to be included in this study Block randomization will be used to divide participants into 2 groups, each with at least 18 participants: Group 1 (MI group) and Group 2 (Control group) (Randomizer.org). Both groups will receive a 4-week physical therapy program. MI (Motor Imagination) group will receive a motor imagination program in addition to the physical therapy program. Data will collect using the visual analog scale (VAS), goniometric measurement, circumference measurement, Disabilities of the Arm, Shoulder, and Hand Questionnaire (DASH), Kinesthetic and Visual Imagery Questionnaire- KVIQ-20, Tampa Kinesiophobia Scale, 3-question satisfaction questionnaire, superficial Electromyography (EMG) (BTS Bioengineering Free EMG 100 RT). Practice Implications: The current study will contribute to understanding how motor imagination affects muscle activity and muscle atrophy.
Status | Not yet recruiting |
Enrollment | 36 |
Est. completion date | July 15, 2026 |
Est. primary completion date | July 15, 2026 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 65 Years |
Eligibility | Inclusion Criteria: - Ability to speak and understand Turkish - Previous arthroscopic rotator cuff repair - Achieving a minimum of 40 points on the Kinesthetic and Visual Imagery Questionnaire -20 (KGIA-20) - Access to adequate technological devices for communication and follow-up Exclusion Criteria: - Who with neurological diseases that may cause functional impairment. - Patients who have another shoulder problem and/or have had previous shoulder surgery on the same upper extremity. - Who wanted to leave the study at their own request - Who could not continue to work due to any additional discomfort developed |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Alanya Alaaddin Keykubat University | Alanya Allaaddin Keykubat University Hospital, Alanya Hamdullah Emin Pasha University, Pamukkale University |
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change of Muscle activity | Change of Muscle activity will be evaluated with superficial Electromyography (EMG) (BTS Bioengineering Free EMG 100 RT). | 1 week before surgery and week 8 after surgery | |
Primary | Change of shoulder functional level | Disabilities of the Arm, Shoulder, and Hand Questionnaire (DASH) will be used to determine the upper extremity functional level.The total of all item scores was then used to calculate the interrogation score, which ranged from 0 (no disability) to 100. (most severe disability). The first 20 questions concern physical competence, while the last ten concern pain and functional and environmental limitations. | 1 week before surgery and week 8 after surgery | |
Primary | Change of Kinesthetic and visual imagery levels | The Kinesthetic and Visual Imagery Questionnaire- KVIQ-20 will be used to assess the kinesthetic and visual imagery levels of healthy and physically disabled individuals.The questionnaire contains a total of 20 titles, 10 of which are visual and 10 of which are kinesthetic. The intensity level of imagery is recorded on a 5-point Likert scale with the questionnaire (5 = appearance of a live image; 1 = no image or sensation). | 1 week before surgery and week 8 after surgery | |
Primary | Change of Kinesiophobia | Kinesiophobia was evaluated with Tampa Scale of Kinesiophobia (TSK).TSK is a 17-question checklist. The scale employs a 4-point Likert scoring system (1= strongly disagree, 4= completely agree). | 1 week before surgery and week 8 after surgery | |
Primary | Change of Patient Satisfaction | A Numerical Evaluation Scale will be used to evaluate a 2-question satisfaction questionnaire. This scale is made up of a horizontal straight line 10 cm long. The line has a value of 0 at the start and a value of 10 at the end, from left to right. On a scale of 0 to 10, patients will be asked to rate their level of satisfaction. | 1 week before surgery and week 8 after surgery | |
Secondary | Descriptive Information | Age, gender, dominant hand, previous diseases, occupation and contact information of the patients were recorded in the descriptive information form. | 1 week before surgery | |
Secondary | Change in Pain-Visual analog scale | Pain of patients during sleep, rest and activity will evaluate using a visual analog scale (VAS).This scale is made up of a 10 cm horizontal straight line. When viewed from left to right, a 0 at the start of the line indicates no pain, and a 10 at the end indicates severe pain. | 1 week before surgery, week 4 and week 8 after surgery | |
Secondary | Change of Range of Motion | The limitation of shoulder joint flexion, extension, abduction, adduction, internal and external rotation movements will be measured using a universal goniometer and recorded in degrees(°). | 1 week before surgery, week 4 and week 8 after surgery | |
Secondary | Change in muscle atrophy | For changes in muscle atrophy, circumference measurements (one of Anthropometric measurements) will be used. | 1 week before surgery and week 8 after surgery |
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