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Effectiveness of FACoT for Individuals Post Stroke

B

Bait Balev Hospital

Status

Completed

Conditions

Stroke

Treatments

Other: FaCoT

Study type

Interventional

Funder types

Other

Identifiers

NCT02925637
adamit_t

Details and patient eligibility

About

To develop and assess the effectiveness of a novel cognitive-functional intervention (FACoT) in occupational therapy for people after mild to moderate stroke.

Enrollment

66 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • >18 years
  • at least three years post stroke
  • severity mild to moderate (NIHSS≤5)
  • independent prior to the stroke
  • can understand and speak Hebrew

Exclusion criteria

  • with no other neurological or psychiatric conditions
  • without dementia

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

66 participants in 2 patient groups

FACoT group
Experimental group
Description:
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
Treatment:
Other: FaCoT
control group
No Intervention group
Description:
control group receiving standard care - cognitive and functional assesment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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