Suprascapular Nerve Block and Proprioception in Hemiplegic Shoulder Pain: A Randomized Controlled Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorFatih Sultan Mehmet Training and Research Hospital

About this trial

The purpose of this prospective randomized controlled clinical trial is to evaluate the effect of suprascapular nerve block on shoulder joint proprioception in stroke patients with hemiplegic shoulder pain.

Fourteen patients aged 18-80 years with hemiplegic shoulder pain will be randomized into two groups. One group will receive suprascapular nerve block followed by a standardized physical therapy program, while the control group will receive the same physical therapy program alone.

The primary outcome is shoulder joint proprioception. Secondary outcomes include pain intensity, shoulder range of motion, motor recovery, stroke-specific quality of life, and upper extremity functional outcomes.

The results of this study are expected to clarify the role of suprascapular nerve block on proprioception and rehabilitation outcomes in patients with hemiplegic shoulder pain.

Eligibility criteria

Qualifiers

Age between 18 and 80 years

Presence of shoulder pain on the hemiplegic side with a Numeric Rating Scale (NRS) score > 3

At least 1 month since the cerebrovascular event (subacute and chronic stroke patients)

Active shoulder flexion range of motion > 90 degrees (required for the application of the laser pointer-assisted joint position sense test)

Disqualifiers

Mini-Mental State Examination score < 24 indicating cognitive impairment

Presence of aphasia

Shoulder spasticity with a Modified Ashworth Scale score > 2

Brunnstrom upper extremity motor stage < 3

Trial design

Treatments tested in this trial

  • suprascapular nerve block
  • physical therapy

Treatment groups

40 Participants
are divided into 2 treatment groups