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Using A Soft Robot to Assist Hand Function in Stroke Patients

Using A Soft Robot to Assist Hand Function in Stroke Patients

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190422003
Enrollment
20
Registered
2019-04-25
Start date
2019-03-04
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

Musculoskeletal problems such as severe pain in any joints of the paretic extremity&#44

Interventions

Using a soft robot with switch on. ,Not using a soft robot.,Using a soft robot with switch off.
Experimental Device,No Intervention No treatment,Sham Comparator Device
Study Group,Control Group,Sham/Placebo Group

Sponsors

THE 90TH Anniversary of Chulalongkorn University Scholarship
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) 20 – 80 years of age (2) Diagnosis of hemorrhagic or ischemic stroke (3) The participants can move a proximal part of the affected arm: the Manual Muscle Testing at least grade 3 of arm and less than grade 3 of hand (the participants can move upper extremity against gravity but cannot grasp something effectively). (4) Sufficient cognitive and language abilities to understand and follow instructions. (5) Adequate balance while seating at least 30 minutes. (6) Vital signs, neurological signs and medical conditions are stable. (7) The participants must leave therapy or training of hand function before the assessment for the recruitment at least 48 hours.

Exclusion criteria

Exclusion criteria: Musculoskeletal problems such as severe pain in any joints of the paretic extremity, instability of the wrist in the affected arm, etc. Mental disorders and cognitive impairment: Thai Mental State Examination (TMSE) score ≤23 Contracture of shoulder joint, elbow joint, wrist joint and finger in the affected arm that hinders to use a soft robot. Stroke patient who has ataxia or severe incoordination The participants cannot wear a soft robot, such as allergic material case, etc.

Design outcomes

Primary

MeasureTime frame
Box and Block Test Score 60 minutes Score/Experimental Study,Action Reach Arm Test Score 60 minutes Score/Experimental Study

Secondary

MeasureTime frame
Satisfaction and Facilitation Survey Score 15 minutes Score/Questionnaire and Interview

Countries

Thailand

Contacts

Public ContactWachirayongyot Thimabut

Chulalongkorn University

wachirayongyot@gmail.com088-6194819

Outcome results

None listed

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