Safety and feasibility evaluation of the novel arm motion measurement device evaluatio for central nerve disorder patients

Safety and feasibility evaluation of the novel arm motion measurement device evaluatio for central nerve disorder patients - Evaluation of the novel upper arm motion measurement device

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000022874

Enrollment

Registered

2016-07-01

Start date

2016-07-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

dysfunction of voluntary movement

Interventions

/Single time intervention /Repeat up to 200 times of arm reach movement with a new robot manipulandum. /maximum 1hour

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: /They can perform the reach movement about 10 cm on the horizontal plane desk. /For around one hour, they can sit down on a chair.

Exclusion criteria

Exclusion criteria: /The condition of their disease is not stable. /They have cognitive impairment, and cannot understand the task. /In everyday life, there is defect in eyesight of the degree to need consideration for movement to need sight information, field of vision, the space recognition. /A finger has the skin damage. /A finger has an osteoarticular disease.

Design outcomes

Primary

Measure	Time frame
/adverse reaction	—

Countries

Japan

Contacts

Public ContactTomoyuki Ueno

Department of Rehabilitation, University of Tsukuba Hospital Department of Rehabilitation

uenot@md.tsukuba.ac.jp029-853-3795

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026