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Effects of upper limb rehabilitation robot EnMotion® in subacute stroke patients: A single blind randomized controlled trial

Effects of upper limb rehabilitation robot EnMotion® in subacute stroke patients: A single blind randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20180902001
Enrollment
30
Registered
2018-09-02
Start date
2018-08-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke stroke&#44

Interventions

Train with EnMotion® 40 min plus conventional occupational therapy 20minutes per day 5 times per week&#44
6 weeks. EnMotion® is rehabilitation robot. It is 5&#45
Bar Linkage system robot&#44
2 degree of freedom. It has display&#44
point hand&#44
forearm bar&#44
CPU. It can multiple mode of movement&#44
visual feedback to patients. Electronic device of EnMotion® is guarantee by European Union.,Train with conventional occupational therapy 60 minutes per day 5 times per week&#44
6 weeks.
Experimental Device,Active Comparator Device
EnMotion® robotic rehabilitation and conventional therapy,conventional occupational therapy

Sponsors

Rehabilitation medicine department, Faculty of medicine, Chulalongkorn university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-85 year 2. First diagnosis stroke and confirmed with CT scan and/or MRI 3. Unilateral weakness 4. Moderate to severe impairment (Fugl-Meyer Assessment = 0 - 47)

Exclusion criteria

Exclusion criteria: 1. unstable vital signs 2. severe cognitive impairment or severe aphrasia (can&#39;t follow protocol) 3. pain VAS > 4 4. ROM shoulder Forward flexion20&#44; flexion=3 7. TMSE <23 8. Visual impairment < 2 meter 9. no cerebellum or brain stem lesion that limit protocol ex severe ataxia 10. receive other upper extremities robotic rehabilitation in 3 month 11. receive other neuromodulation in 3 month

Design outcomes

Primary

MeasureTime frame
Motor control function of upper extremities at end of rehabilitation (6wk atfer start rehabilitation) Fugl&#45;Meyer Assessment

Secondary

MeasureTime frame
Motor capacity function of upper extremities at end of rehabilitation (6wk atfer start rehabilitation) Action Research Arm Test,Activity daily living at end of rehabilitation (6wk atfer start rehabilitation) Barthel Index (BI),Spasticity at end of rehabilitation (6wk atfer start rehabilitation) Modified Ashworth Scale (MAS),Motor power at end of rehabilitation (6wk atfer start rehabilitation) Medical Research Council (MRC),Motor recovery stage at end of rehabilitation (6wk atfer start rehabilitation) Brunnstrom Stages of Motor Recovery (BRS): ,Number of repetition in robot session at end of rehabilitation (6wk atfer start rehabilitation) Number of repetition in robot session,end&#45;point hand velocity (cm/s) at end of rehabilitation (6wk atfer start rehabilitation) end&#45;point hand velocity (cm/s),Satisfaction scale of patient at end of rehabilitation (6wk atfer start rehabilitation) Satisfaction scale of patient,Satisfaction scale of therapist at end of rehabilitation (6wk atfer start rehabilitation) Satisfaction scale of therapist

Contacts

Public ContactChat Iamsirikij

Rehabilitation medicine department&#44; faculty of medicine&#44; Chulalongkorn University

chatfilm@gmail.com0898159518

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026