Safety and effect on shoulder joint of a novel shoulder rehabilitation device

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002696

Enrollment

Registered

2018-02-14

Start date

2017-03-21

Completion date

Unknown

Last updated

2019-03-11

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

Conditions

None listed

Interventions

Others(rehabilitation robot) : We developed a novel robot with one arm to perform shoulder rehabilitation therapy. This robot performed joint mobilization and stretching exercise with laying the patie

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Subacute stroke patients who reported hemiplegic shoulder pain with a minimum visual analogue scale (VAS) of 3 points (0-10 point scale) were recruited for 12 months consecutively from July, 2016.

Exclusion criteria

Exclusion criteria: 1) significant cognitive impairment (Korean version of Mini-Mental State Examination, K-MMSE <15) or language deficits that might affect the reliability of responses to outcome measure scales, 2) pre-existing shoulder pain prior to stroke, and 3) definite shoulder dislocation of affected limb as seen on radiographs due to safety concern.

Design outcomes

Primary

Measure	Time frame
visual analogue scale	—

Secondary

Measure	Time frame
Passive range of motion of shoulder, PROM;Korean version of Shoulder disability questionnaire, K-SDQ;Ultrasonographic grading	—

Countries

Korea, Republic of

Contacts

Public ContactMINSU KIM

Wonkwang University Hospital

helmaine@naver.com+82-63-859-1610

Outcome results