Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
10 participants
INTERVENTIONAL
2024-10-11
2025-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DEVICE_FEASIBILITY
NONE
Study Groups
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RehAtt
Each patient was included in the introduction session (performed by a psychologist), three sessions of occupational therapy and three sessions of physiotherapy. Each session lasted for 30 minutes. Occupational-therapy training was focused on activities aimed at improving upper limb function; physiotherapy training was focused on balance, walking and standing.
RehAtt
Each patient received the RehAtt intervention.
Interventions
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RehAtt
Each patient received the RehAtt intervention.
Eligibility Criteria
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Inclusion Criteria
* one-sided hemiparesis,
* adequate cognitive abilities.
Exclusion Criteria
* aphasia,
* known presence of an epileptic seizure in the last year,
* other orthopaedic and neurological diseases affecting sensory or motor functions,
* inability to sit independently,
* severe visual impairment,
* severe depression.
18 Years
ALL
No
Sponsors
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University Rehabilitation Institute, Republic of Slovenia
OTHER
Responsible Party
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Principal Investigators
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Nataša Bizovičar, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
University Rehabilitation Institute, Republic of Slovenia
Locations
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University Rehabilitation Institute, Republic of Slovenia
Ljubljana, , Slovenia
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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URIS202403
Identifier Type: -
Identifier Source: org_study_id
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