Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 2:58 PM
Ignite Modification Date: 2025-12-24 @ 2:58 PM
NCT ID: NCT06270459
Eligibility Criteria: Inclusion Criteria: 1. Clinical stroke (ischaemic or haemorrhagic) confirmed by admitting doctors and CT, CT angiography or MRI brain imaging. 2. Age 21 to 90 years, both males and females. 3. At least \> 28 days post stroke. 4. Upper limb motor impairment of Fugl-Myer Motor Assessment (FMA) scale 10 to 60 5. Has a stable home abode and a carer/ NOK to supervise home based exercise. 6. Ability to sit supported continuously for 60 minutes. 7. Montreal Cognitive Assessment (MOCA) score \> 21/30 8. Able to understand purpose of research and give consent. Exclusion Criteria: 1. Non-stroke related causes of arm motor impairment. 2. Medical conditions incompatible with research participation: uncontrolled medical illnesses (hypertension or diabetes, ischaemic heart disease, congestive heart failure, bronchial asthma, end stage renal/liver/heart/lung failure, unresolved cancers. 3. Anticipated life expectancy of \< 6 months. 4. Inability to tolerate sitting continuously for 60 minutes. 5. Local factors potentially worsened by intensive robot-aided arm therapy and computer-based training: active seizures within 3 months, spasticity of Modified Ashworth Scale grades \>2 skin wounds, shoulder, arm pain VAS \> 5/10, active upper limb fractures, arthritis, fixed upper limb flexion contractures. 6. Hemianesthesia of affected limb. 7. History of dementia, severe depression, agitation, or behavioural problems. 8. Pregnancy or lactation in females 9. Absence of reliable carer to provide supervision during home training
Healthy Volunteers: False
Sex: ALL
Minimum Age: 21 Years
Maximum Age: 90 Years
Study: NCT06270459
Study Brief:
Protocol Section: NCT06270459