WEARABLE SYSTEM FOR FUGL-MEYER ASSESSMENT-UPPER EXTREMITY IN STROKE PATIENT

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

TCTR

Registry ID

TCTR20190708004

Enrollment

Registered

2019-07-08

Start date

2019-07-04

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

Stroke patient FMA Fugl&#45

Interventions

one time trial &#45

Assessment by Expert 30 minute &#45

Assessment by System 30 minute

Experimental Device

WAAM Group

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Minimum 18 years old Stroke with hemiparesis Good consciousness Constant normal vital sign Nerve system has been in good condition at least 48 hours Can sit continuously at least 30 minutes Have not participated in any research that related to upper extremity Subject commits to paticipate in the trial

Exclusion criteria

Exclusion criteria: Have complex regional pain syndrome rotator cuff tendinitis Upper extremity have pain condition spastic Modified Ashworth Scale (MAS) > 2 Severe aphasia Mild to severe depression

Design outcomes

Primary

Measure	Time frame
Fugl-Meyer Assessment-upper extremity section (From Expert) 04/10/2019 Point ,Fugl-Meyer Assessment-upper extremity section (From system) 04/10/2019 Point ,Assessment Time (Expert uses) 04/10/2019 Minute : Second,Assessment Time (System uses) 04/10/2019 Minute : Second	—

Secondary

Measure	Time frame
Satisfactory of the system (From participant) 04/10/2019 Level,Satisfactory of the system (From Expert) 04/10/2019 Level	—

Countries

Thailand

Contacts

Public Contactworapong narongwongwathana

Chularongkorn University

tuworapong@gmail.com0944931979

Outcome results

None listed

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

WEARABLE SYSTEM FOR FUGL&#45;MEYER ASSESSMENT&#45;UPPER EXTREMITY IN STROKE PATIENT