Stroke Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have had a stroke (either a blocked blood vessel or a bleed in the brain), confirmed by doctors and brain scans
- People aged 21 to 80 years, of any gender
- People who are at least 28 days past their stroke
- People with a certain level of arm and hand weakness, as measured by a specific movement assessment (confirm with trial site for exact score range)
- People who score above 21 out of 30 on a standard memory and thinking test
- People who are able to sit with support for 60 minutes continuously
- People who have a stable home with enough space to set up the trial equipment
- People who have a carer or family member available to supervise home-based exercises
Who may not be able to join:
- People whose arm weakness is caused by a condition other than stroke
- People with serious uncontrolled health conditions, such as uncontrolled high blood pressure, diabetes, heart disease, heart failure, asthma, severe or untreated depression, agitation, advanced kidney, liver, heart or lung failure, or ongoing cancer
- People whose life expectancy is estimated to be less than 6 months
- People who have a pacemaker or other active implanted medical device
- People who have had a seizure within the past 3 months
- People with significant muscle stiffness in the affected arm, as measured by a standard scale (confirm with trial site for exact score)
- People with severe pain in the affected arm, rated above 5 out of 10 on a pain scale
- People with open skin wounds
- People whose thinking or memory difficulties would prevent them from taking part in the study
- People with severe vision problems or difficulty paying attention to one side of their visual field that would affect use of the trial technology
- People with a history of dementia, depression, or behavioural problems
- People who are pregnant or breastfeeding
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Kuah Wee Keong Christopher, Tan Tock Seng Hospital
Phone: 68894580
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
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Trial details
Where this trial is recruiting
Primary endpoints
Compliance Rates
Can't join this trial?
Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.