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Recruiting NCT06677320

Establishing Clinical Significance in Rotator Cuff Disease

Observational Rotator Cuff Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Exercise.
Who it may be relevant to
Registry conditions: Rotator Cuff Disease. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Establishing the Clinical Significance Values of Scales Used in Rotator Cuff Disease

Overview

The goal of this observational study is to learn about rotator cuff patients. The main questions it aims to answer are: * What is the minimal clinically important difference value of the Shoulder Disability Questionnaire, the short version of the Western Ontario Rotator Cuff Index, the Shoulder Rating Questionnaire, and the University of California-Los Angeles Shoulder Scale? * What is the substantial clinical benefit value of the Shoulder Disability Questionnaire, the short version of the Western Ontario Rotator Cuff Index, the Shoulder Rating Questionnaire, and the University of California-Los Angeles Shoulder Scale? * What is the patient-acceptable symptomatic state value of the Shoulder Disability Questionnaire, the short version of the Western Ontario Rotator Cuff Index, the Shoulder Rating Questionnaire, and the University of California-Los Angeles Shoulder Scale? * What is the maximal outcome improvement value of the Shoulder Disability Questionnaire, the short version of the Western Ontario Rotator Cuff Index, the Shoulder Rating Questionnaire, and the University of California-Los Angeles Shoulder Scale? * What are the risk factors that prevent rotator cuff patients from reaching the minimal clinically important difference value? * What are the risk factors that prevent rotator cuff patients from reaching the substantial clinical benefit value? * What are the risk factors that prevent rotator cuff patients from reaching the patient-acceptable symptomatic state value? * What are the risk factors that prevent rotator cuff patients from reaching the maximal outcome improvement value?

Interventions

  • Other Exercise
    Patients with rotator cuff disease will receive exercise treatment for two months.

Primary outcome measures

  • Functional level [Time frame: before the treatment and within 1 week after 2 months of treatment]
  • Functional level [Time frame: before the treatment and within 1 week after 2 months of treatment]
  • Functional level [Time frame: before the treatment and within 1 week after 2 months of treatment]
  • Functional level [Time frame: before the treatment and within 1 week after 2 months of treatment]

Eligibility criteria

Inclusion criteria

  • to be over 18 years old
  • to be a rotator cuff patient

Exclusion criteria

  • to have another pathology in the affected shoulder area
  • to have a neurological, rheumatological, or oncological disease
  • to have radiculopathy
  • to have had a previous fracture or operation in the affected shoulder area
  • to be not cooperative enough for what will be done within the scope of the study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

Turkey (Türkiye) · 1 center
  • Kırklareli Eğitim ve Araştırma Hastanesi — Kırklareli

Identifiers

NCT: NCT06677320 · 2024-1636

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗