A Multidisciplinary Telerehabilitation for Stroke Patients
NCT ID: NCT04116190
Last Updated: 2019-10-04
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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COMPLETED
NA
45 participants
INTERVENTIONAL
2017-09-01
2018-05-31
Brief Summary
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Design: Chronic stroke patients eligible for multidisciplinary rehabilitation funded by the Social Insurance Institution were enrolled between September 2017 and March 2018 in a consecutive basis to receive a mixed program of inpatient rehabilitation and telerehabilitation in their homes or a traditional inpatient rehabilitation only.
Intervention: A rehabilitation course with a 3-day inpatient stay followed by an 8-week telerehabilitation period completed by 2-day evaluation stay in a rehab center. The control group received conventional multidisciplinary rehabilitation for two weeks in an inpatient setting.
Outcome and measures: Change in the Finnish version of Functional Status Questionnaire (FSQFin), the World Health Organization Quality of Life - Short version (WHOQOL-Bref), the Barthel Index, the Beck Depression Inventory (BDI21), and the Goal Attainment Scale (GAS) and a patient satisfaction questionnaire.
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Telerehabilitation (TR)
Shortened inpatient rehabilitation mixed with home-based telerehabilitation.
Telerehabilitation
Short inpatient multidisciplinary rehabilitation followed by home-based telerehabilitation and a short evaluation period at the end of it.
Conventional rehabilitation (CR)
Traditional inpatient rehabilitation
Conventional inpatient rehabilitation
Multidisciplinary inpatient rehabilitation, no adjustments due to the study.
Interventions
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Telerehabilitation
Short inpatient multidisciplinary rehabilitation followed by home-based telerehabilitation and a short evaluation period at the end of it.
Conventional inpatient rehabilitation
Multidisciplinary inpatient rehabilitation, no adjustments due to the study.
Eligibility Criteria
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Inclusion Criteria
* eligible to receive rehabilitation funded by the Social Insurance Institution (meets the criteria of chronic disability and need for rehabilitation)
* for intervention group: capable to use a personal computer and telecommunication
Exclusion Criteria
* significant problems in hearing, seeing or understanding information related to the intervention
18 Years
ALL
No
Sponsors
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Vetrea Terveys Oy
OTHER
Responsible Party
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Principal Investigators
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Kauko Pitkanen, PhD
Role: STUDY_DIRECTOR
VetreaNeuron
Locations
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Vetrea
Kuopio, Northern Savonia, Finland
Countries
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Other Identifiers
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Aimo2019
Identifier Type: -
Identifier Source: org_study_id
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