To Evaluate the Therapeutic Effect of Laser Acupuncture in Patients With Acute or Subacute Post Stroke Shoulder Pain
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Post Stroke Shoulder Pain
In brief
Investigators propose a research design protocol to evaluate the efficacy of laser acupuncture in improving shoulder pain and improving shoulder function recovery after stroke.
Key facts
- Study ID
- NCT05328401
- Run by
- Chang Gung Memorial Hospital
- People needed
- 58
- Starts
- 2022-04-16
- Expected to finish
- 2028-03-15
- Last updated by the study team
- 2026-03-06
Who can join
Age: 20 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Beyond the age of 20.
- Normal consciousness before and after stroke who can reply and fill in the questionnaire.
- Subacute (subacute phase: 7 days to 6 months after stroke) and Chronic (chronic phase: more than 6 months after stroke) with shoulder pain after stroke and in post- stroke recovery period.
- Stop taking painkillers for more than 1 day,
- Without received intramuscular drugs (steroids, botulinum toxin, glucose, etc.) injections in the shoulder joint or around the shoulder for more than 2 weeks
- Those willing to sign the written subject consent form.
You may not qualify if…
- Participants with shoulder pain symptoms before the stroke
- Acute shoulder trauma on the affected side of shoulder pain in the past.
- Surgery on the affected side of shoulder pain in the past.
- Those who cannot complete the scale assessment due to aphasia, post-stroke depression, and obvious cognitive impairment.
- Women who are pregnant or planning to become pregnant.
- Those who have a history of epilepsy and are receiving anti-epileptic drug treatment.
- Who are receiving any herbal or folk remedies related to shoulder pain.
- Any other conditions deemed unsuitable in the assessment of the responsible physician.
- Those who have not signed the written subject consent form.
Where it is running
- Chang Gung Memorial Hospital, Keelung Medical Center — Keelung, Taiwan, Taiwan (enrolling)
Full record on ClinicalTrials.gov
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