A Qualitative and Usability Evaluation of Advanced Technologies for Home Upper Limb Neurorehabilitation Post-stroke

ConditionStroke
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-80
SponsorTan Tock Seng Hospital

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

Treatment groups

30 Participants
are divided into 1 treatment group

Sponsors and collaborators