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) that was confirmed by doctors using brain scans such as a CT or MRI.
- People aged between 21 and 90 years old, of any gender.
- People who are at least 28 days past their stroke.
- People with a moderate level of arm weakness or movement difficulty, as measured by a standard assessment tool called the Fugl-Meyer Motor Assessment (confirm with trial site for exact score range).
- People who have a stable home to live in and a family member or carer who can supervise home-based exercises.
- People who are able to sit upright with support for 60 minutes continuously.
- People who score above 21 out of 30 on a standard memory and thinking test called the Montreal Cognitive Assessment.
- People who are able to understand the purpose of the research and agree to take part.
Who may not be able to join:
- People whose arm weakness or movement difficulty is caused by something other than a stroke.
- People with serious or uncontrolled health conditions, such as uncontrolled high blood pressure or diabetes, heart disease, heart failure, severe asthma, end-stage kidney, liver, heart or lung failure, or active cancer.
- People who are not expected to live for more than 6 months.
- People who are unable to sit continuously for 60 minutes.
- People with certain conditions affecting the arm that could be made worse by intensive robot-assisted therapy, including seizures within the past 3 months, significant muscle stiffness, open skin wounds, severe arm or shoulder pain, an active broken bone in the arm, arthritis, or permanent stiffening of the arm joints.
- People who have lost sensation across an entire side of the body, affecting the arm involved in the trial.
- People with a history of dementia, severe depression, agitation, or significant behavioural difficulties.
- Women who are pregnant or breastfeeding.
- People who do not have a reliable carer available to supervise home training sessions.
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: Karen Chua, Tan Tock Seng Hospital
Phone: 68894580
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Compliance Rates
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.