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A study to investigate the effect of rehabilitation using visual information for people who have difficulty feeling body leaning after stroke.

Therapeutic effects of delayed visual feedback on cerebrovascular disorder patients exhibiting the pusher behavior: A double-blind randomized crossover trial - A double-blind randomized crossover trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060093
Enrollment
40
Registered
2025-12-22
Start date
2025-12-25
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

cerebrovascular disease

Interventions

Delayed visual feedback. The duration is 1 week, with 30 weight transfers to the nonparalyzed side per day. Visual feedback. The duration is 1 week, with 30 weight transfers to the nonparalyzed side p

Sponsors

other
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with hemiplegia due to first stroke with or suspected of having Pusher behavior who are hospitalized in a convalescent ward. Able to understand simple instructions.

Exclusion criteria

Exclusion criteria: Patients with concurrent disability of submental lesions, bilateral disability, psychiatric disorders, pre-existing orthopedic diseases that interfere with ADL, and sequelae of hemiplegia after stroke.

Design outcomes

Primary

MeasureTime frame
Burke lateropulsion scale(BLS) (before intervention, after intervention1, after intervention2)

Secondary

MeasureTime frame
Scale for Contraversive Pushing (SCP) Subjective postural vertical(SPV) Trunk Control Test (TCT) Eye opening, eye closing, left and right center of gravity trajectory length, left and right center of gravity shift distance, and left and right maximum load ratio using a seat pressure gauge.

Countries

Japan

Contacts

Public ContactYuichi Kato

Moriyama Neurological Center Hospital Department of Rehabilitation

yu1ii10122101@outlook.com03-3675-1211

Outcome results

None listed

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