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Active, not recruiting Not applicable

Effects of Externally Focused Shoulder Stabilization Exercises on Individuals With Rotator Cuff Tendinopathy

NCT06702319 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-07-01
Last updated
2024-11-26

Condition(s) studied

Shoulder PainRotator Cuff Tendinitis

Investigational drug(s) / intervention(s)

Exercise

Exercise: Home exercises and home exercises with internal focus exercises or external focus exercises

Study summary

This study aims to evaluate the effectiveness of externally focused shoulder stabilization exercises on range of motion, pain, handgrip strength, and proprioception in patients with rotator cuff tendinopathy. For the study, 69 patients will be randomly divided into three groups: Home Program Group (HPG), Internal Focused Exercise Group (IFEG), and External Focused Exercise Group (EFEG). The treatment period for all three groups will be 6 weeks. Shoulder range of motion, pain, handgrip strength, joint position sense, and shoulder function (WORC and QuickDASH) of the three groups will be evaluated at baseline and after intervention. IFEG will do the exercises with a physiotherapist twice a week. During the exercise, the patient will be allowed to focus on the body parts while performing the movement. EFEG will do the exercises with a physiotherapist twice a week. The patient will be allowed to focus on a point outside the body, namely the effect of the movement, during the exercise. In the management of HPG patients will be provided with an exercise brochure. At the conclusion of the study, the three groups will be compared and evaluated using appropriate statistical analyses to assess the outcomes and determine any significant differences between them.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Having a diagnosis of rotator cuff tendinopathy, * Having sufficient cooperation to perform the exercises. Exclusion Criteria: * Having a neurological problem, * Having a previous fracture in the shoulder region, * Having undergone a relevant surgery in the past, * Having any chronic illness that could prevent exercise (e.g., chronic heart failure, pacemaker, etc.), * Having a systemic condition that could affect proprioception, such as diabetes, rheumatoid arthritis, ankylosing spondylitis, or advanced osteoarthritis, * Having received a physiotherapy program targeting the neck and upper extremity within the last 3 months.

Primary outcome measure(s)

  • Quick Disabilities of Arm, Shoulder & Hand — one day before the intervention and 6 weeks after
    The Quick Disabilities of Arm, Shoulder \& Hand Index is used to measure upper extremity physical function. A Turkish validity and reliability study has been conducted. The scale includes 11 headings extracted from the long version. Each question consists of a 5-point scale. The total score is calculated with the formula \[(sum of n responses) /n-1\] ×25, where n= indicates the total number of questions answered. The total score varies between 0 (no disability) and 100 (severe disability). The final score is classified as; 0- 15: 'no problem', 16-40: 'problem but able to work', 40 and above: 'unable to work'.

Trial sites (1)

FacilityCityRegionStatus
Izmir Democracy University Izmir Turkey (Türkiye)
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06702319 on ClinicalTrials.gov ↗ ← All trials in Turkey