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
66 participants
INTERVENTIONAL
2017-03-12
2020-02-27
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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FACoT group
treatment group will receive FACoT, that include one to one 10 treatment sessions. the treatment sessions will include: functional activities, cognitive activities and strategies (pencil-pen treatment), and behavioural strategies
FaCoT
The intervention will include: functional activities, cognitive activities and strategies (pencil-pen treatment), and behavioural strategies
control group
control group receiving standard care - cognitive and functional assesment
No interventions assigned to this group
Interventions
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FaCoT
The intervention will include: functional activities, cognitive activities and strategies (pencil-pen treatment), and behavioural strategies
Eligibility Criteria
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Inclusion Criteria
* at least three years post stroke
* severity mild to moderate (NIHSS≤5)
* independent prior to the stroke
* can understand and speak Hebrew
Exclusion Criteria
* without dementia
18 Years
ALL
No
Sponsors
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Tel Aviv University
OTHER
Bait Balev Hospital
OTHER
Responsible Party
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Principal Investigators
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tal adamit, PHD student
Role: PRINCIPAL_INVESTIGATOR
Maccabbi health center ashdod isreal
Locations
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Maccabi
Ashdod, , Israel
Countries
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Other Identifiers
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adamit_t
Identifier Type: -
Identifier Source: org_study_id
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