CompletedNot Applicable

Effects of Scapular Stabilization Exercises and Scapular Proprioceptive Neuromuscular Facilitation Technique on Pain, Range of Motion, Functionality, Scapular Dyskinesia and Proprioception in Patients With Rotator Cuff Lesions

Turkey (Türkiye)30 participantsStarted 2023-12-25

Plain-language summary

This study aimed to compare the effects of Scapular Proprioceptive Neuromuscular Facilitation (PNF) applications and Scapular Stabilization exercises on pain, joint range of motion, functionality, scapular dyskinesia, and proprioception in individuals with rotator cuff lesions. The study included 30 volunteer participants aged 18 to 65 years, who had been diagnosed with Rotator Cuff Lesion and reported shoulder pain. The Scapular Stabilization group (n=15) received scapular stabilization exercises in addition to conventional treatment, while the PNF group (n=15) received scapular PNF patterns and techniques in addition to conventional treatment. In this study, the Visual Analog Scale (VAS) was used to evaluate the pain severity of individuals, a universal goniometer was used to measure joint range of motion, and the Disabilities of the Arm, Shoulder, and Hand Questionnaire (DASH) was used to assess functional status. Scapular dyskinesia was evaluated using the Lateral Scapular Shift Test (LSKT) and Scapular Dyskinesia Test (SDT), while proprioception was assessed using the Active Angle Repetition Test. Statistical analysis of the data was performed using SPSS V.27 software.

Who can participate

Age range

18 Years – 65 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Being between 18 - 65 years of age * Getting a diagnosis of Rotator Cuff Lesion, * Presence of unilateral shoulder pain for a minimum of 3 weeks, * Signing the "Informed Voluntary Consent Form", * Individuals who are cooperative and willing to participate in the study. Exclusion Criteria: * Corticosteroid treatment or local corticosteroid injections in the last three months, * Neer Stage 3 tear of the rotator cuff tendons, * Shoulder fracture or instability, * Physiotherapy within the last 6 months on the same shoulder, * History of surgery in the shoulder girdle or thorax, * With cognitive and mental problems, * Individuals with malignancy, neuromuscular disorders, unstable angina, arthritis, cardiopulmonary disorders, vertigo or various vestibular system disorders and communication problems.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Shoulder Pain

Timeframe: 6 weeks

Range of Motion of the Shoulder Joint

Timeframe: 6 weeks

Shoulder Functionality

Timeframe: 6 weeks

Scapular Dyskinesia

Timeframe: 6 weeks

Scapular Dyskinesia

Timeframe: 6 weeks

Shoulder Proprioception

Timeframe: 6 weeks

Trial details

NCT IDNCT06916572

SponsorBiruni University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-07-08

View on ClinicalTrials.gov More Rotator Cuff Lesions trials

Plain-language summary

Who can participate

Age range

18 Years – 65 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.