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Effect of rehabilitation glass on lateropulsion in acute stroke

Effect of rehabilitation glass on patients with lateropulsion in acute stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1052230046
Enrollment
98
Registered
2023-06-20
Start date
2023-06-20
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

acute stroke lateropulsion

Interventions

Intervention is one experiment of wearing rehabilitation glasses within 1-2 weeks after admission. For the intervention, about 20 minutes are needed: 4 minutes for evaluation before wearing rehabilita
rehabiritation glasses, xR technology

Sponsors

Yokota Chiaki
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) aged equal or above 18 and below 85 years old 2) acute stroke patients admitted to SCU withon 48 hours of onset 3) first-ever stroke 4) patients with moderate to severe lateropulsion defined as equal or above 0.75 on the Scale for Contraversive Pushing on registration 5) patiehts with obtained informed consent

Exclusion criteria

Exclusion criteria: 1) communication difficulties due to impaired consciousness (Japan coma scale equal or above 10) , aphasia, and/or cognitive dysfunction 2) difficulty in performing gait training exercises 3) patients who cannot participate in the present study judged by the chief-or co-investigators of the present study.

Design outcomes

Primary

MeasureTime frame
1)Scale for Contraversive Pushing (SCP) Canges of SCP from before to under wearing the rehabilitation glasses.

Secondary

MeasureTime frame
Comparing pre- and post-wearing conditions and pre-wearing and wearing conditions 1) Subscore of Scale for Contraversive Pushing 2) Functional Ambulation Categories 3)Balance sub-score of Fugl Meyer Assessment 4)Motion analysis 5)Patients number withot change of postures after putting the glasses 6)MIsery SCale 7)Simulator Sickness Questionnaire 8)Advers events

Contacts

Public ContactChiaki Yokota

National Cerebral and Cardiovascular Center

yokota.chiaki@ncvc.go.jp+81-6-6170-1069-60245

Outcome results

None listed

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