About this trial
Due to limited resources such as the low therapist to patient ratio or high costs associated to rehabilitation therapy, providing higher therapy dose to patients after discharge is highly challenging. This often results in non-use of the impaired limb as a result of the decreased therapy dose, causing partial loss of the functional improvements previously gained during early rehabilitation.
In this study, the investigators plan to pilot the HomeRehab Gym concept via the deployment of three rehabilitation devices at patients' homes: MyoPanda, H-Man and ReHandyBot.
Eligibility criteria
Qualifiers
Clinical stroke (ischaemic or haemorrhagic) confirmed by admitting doctors and CT, CT angiography or MRI brain imaging
Age 21 to 80 years, both males and females
At least 28 days post-stroke
Upper limb motor impairment of Fugl-Meyer Assessment (FMA) scale 20 to 50
Disqualifiers
Functional impairment of the upper limb due to other pathologies
Medical conditions incompatible with research participation: uncontrolled medical illnesses (hypertension or diabetes, ischaemic heart disease, congestive heart failure, bronchial asthma, severe /untreated depression, agitation, end stage renal/liver/heart/lung failure, unresolved cancers)
Anticipated life expectancy of less than 6 months
Pacemakers and other active implants
Trial design
Treatments tested in this trial
- H-Man Robot
- ReHandyBot
- MyoPanda