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Enrolling by invitation NCT06758986

Is Gender a Factor in Patients With Subacromial Shoulder Pain?

— Observational Subacromial Pain Syndrome

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Subacromial Pain Syndrome. Basic parameters: 18 years — 65 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 →

Unsure about the terms? Read our patient guide →

Official title

Patients With Subacromial Shoulder Pain and Gender

Overview

This study aimed to investigate the effects of gender on pain, functionality, range of motion, disability level and position sense parameters in patients with subacromial shoulder pain.

Primary outcome measures

  • Visual Analog Scale [Time frame: 20 weeks]
Secondary outcome measures (3)
  • Quick DASH [Time frame: 20 weeks]
  • SPADI [Time frame: 20 weeks]
  • The laser-pointer assisted angle reproduction test [Time frame: 20 weeks]

Eligibility criteria

Inclusion criteria

  • Being between the ages of 18-65
  • Being diagnosed with unilateral subacromial impingement syndrome
  • Not having received steroid injections or physical therapy for shoulder problems in the last 6 months
  • Having painful shoulder pain for the last 3 months
  • Being willing to participate in the study

Exclusion criteria

  • Having a rheumatic, neurological, cardiovascular, psychiatric or systemic disorder
  • Having a surgical operation on the shoulder, cervical and thoracic region
  • Having a neurological deficit, fracture or history of fracture in the upper extremity
  • Having cervical radiculopathy
  • Having communication problems

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

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Turkey (Türkiye) · 1 center
  • Kirsehir Ahi Evran University — Kırşehir

Identifiers

NCT: NCT06758986 · KAEU-T.ATAHAN-010

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗