Stroke Hemiplegic Shoulder Pain: Ultrasound Findings and VAS (Cross-Sectional)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorAnkara Etlik City Hospital

About this trial

Hemiplegic shoulder pain is a frequent complication after stroke and may be associated with structural abnormalities detectable by musculoskeletal ultrasound. This prospective cross-sectional observational study aims to evaluate the relationship between shoulder ultrasound abnormality score and pain severity in patients with post-stroke hemiplegic shoulder pain. Pain severity will be assessed using the Visual Analog Scale (VAS) for rest, movement, and night pain. Shoulder ultrasound will be performed using a standardized scoring system to quantify structural abnormalities. The primary objective is to investigate whether ultrasound abnormality burden is associated with pain severity in different clinical conditions (rest, exercise, and night).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Being between 18-75 years of age

Patients with a history of stroke within the last 2 weeks to 6 months

Patients with shoulder pain on the hemiplegic side

Mini-mental status test score >25

Disqualifiers

Motor aphasic patient group

Patients with a history of previous surgery on the hemiplegic shoulder for any reason

Those with other diseases that can explain the shoulder pain

Those with neurodegenerative diseases that cause impairment in cognitive functions, such as dementia

Trial population

Adult patients with stroke and hemiplegic shoulder pain who are admitted to the physical medicine and rehabilitation clinic of Ankara Etlik City Hospital will be included. Eligible patients are between 18 and 75 years of age and within 2 weeks to 6 months after stroke. All participants will undergo clinical assessment and shoulder ultrasound examination at admission.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

100 Participants
are grouped into 1 trial group
Group A: Post-stroke Hemiplegic Shoulder Pain Patients

Trial outcomes

Primary outcomes

1

Association between shoulder ultrasound abnormality score and pain severity

Relationship between total shoulder ultrasound abnormality score and Visual Analog Scale (VAS) pain scores (rest, movement, and night pain) assessed at admission.

Time frame
At admission (single assessment on the same day as ultrasound)

Secondary outcomes

Other outcomes

Sponsors and contacts

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