Stroke Trial, Recruiting NCT06076928 Sponsor: Tan Tock Seng Hospital Condition: Stroke
Back to Stroke

Stroke Trial, Recruiting

NCT06076928
Recruiting Not Applicable

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 aged 21 to 85 years, both male and female
  • People who have had their first-ever stroke (either a blocked blood vessel or a bleed in the brain), confirmed by a specialist doctor or brain scan
  • People who are more than 16 weeks past their stroke
  • People whose stroke has caused weakness on one side of the body in a pattern typical of stroke
  • People with at least some ability to lift the shoulder and bend the elbow (at a certain minimum strength level, confirm with trial site)
  • People with varying levels of weakness in the fingers and thumb of the affected hand (confirm with trial site for exact range)
  • People whose wrist and hand movement score falls below a certain level on a standard stroke assessment (confirm with trial site)
  • People with limited or no muscle stiffness in the thumb, index, and middle fingers
  • People who can feel a pin-prick sensation in their thumb and index finger
  • People whose hand size falls within a specific range (170–200mm long and 75–85mm wide) that fits the robotic glove used in the trial
  • People whose brain signals are compatible with a brain-computer interface (BCI) device, as assessed by a standard screening test
  • People who can understand simple instructions and score above a certain level on a basic memory and thinking test
  • People who are able to give their own informed consent to participate

Note: People whose brain signals are not compatible with the BCI device may still be considered for a different part of the trial (confirm with trial site).


Who may not be able to join:

  • People who have had more than one stroke
  • People diagnosed with a brain or nerve condition that gets worse over time, such as Parkinson's disease, dementia, or ALS
  • People with unstable or serious medical or neurological conditions, or a life expectancy of less than 6 months
  • People on dialysis due to kidney failure
  • People with severe heart failure
  • People with a condition where blood pressure drops significantly when standing up
  • People with a history of uncontrolled serious infections
  • People who have had an epileptic seizure within 3 months of the study consent date
  • People with skin conditions on the hand or arm that could be made worse by wearing a robotic glove, such as open wounds, ulcers, eczema, or active skin infections
  • People who are unable to sit upright for at least 90 minutes (with rest breaks)
  • People with severe difficulty speaking or understanding language, severe visual problems or neglect, untreated severe depression, or a psychiatric illness that would prevent them from taking part
  • People with significant muscle stiffness (spasticity) in the affected arm or hand above a certain level
  • People experiencing moderate to severe pain in the affected hand or arm
  • People with finger contractures, severely limited hand or wrist movement, active bone fractures, or arthritis causing joint deformity
  • People with severe uncontrolled limb movement problems (ataxia or apraxia)
  • People with severely reduced sensation across the entire affected arm
  • People whose brain signals for imagined movement cannot be detected by the BCI device
  • People who have had part of their skull removed (craniectomy), as this may affect how the BCI device fits
  • People currently taking part in another interventional research trial
  • People living in a nursing home or overseas who may not be able to attend the research site regularly
  • 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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Tan Tock Seng Hospital
Registry
ClinicalTrials.gov
Start date
1 August 2024
Est. completion
1 January 2026

Where this trial is recruiting

🇸🇬 Singapore

Primary endpoints

Action Research Arm Test (ARAT) Score

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov