Effectiveness of a Novel Meta-cognitive-functional Intervention (FACoT) for Individuals Post Mild-moderate Stroke

Bait Balev Hospital1 site in 1 country66 target enrollmentMarch 12, 2017

ConditionsStroke

Overview

Phase: N/A
Intervention: Not specified
Conditions: Stroke
Sponsor: Bait Balev Hospital
Enrollment: 66
Locations: 1
Primary Endpoint: Change in scores of The Canadian Occupational Performance Measure (COPM)
Status: Completed
Last Updated: 5 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

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

Registry

clinicaltrials.gov

Start Date

March 12, 2017

End Date

February 27, 2020

Last Updated

5 years ago

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

Bait Balev Hospital

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

Not provided

Exclusion Criteria

•with no other neurological or psychiatric conditions
•without dementia

Outcomes

Primary Outcomes

Change in scores of The Canadian Occupational Performance Measure (COPM)

Time Frame: Change between baseline (week 0) to time 1 (post-intervention -10-13 weeks later) and time 2 (follow-up- three month later)

Secondary Outcomes

Change in scores of Reintegration to Normal Living Index (RNL)(Change between baseline (week 0) to time 1 (post-intervention, 10-13 weeks later) and between baseline to time 2 (follow-up-3 month later))
Change in scores of Short Form-12v2 Health Survey (SF-12v2)(Change between baseline (week 0) to time 1 (post-intervention, 10-13 weeks later) and between baseline to time 2 (follow-up- 3 month later))
Change in scores of zoo-map(Change between baseline (week 0) to time 1 (post-intervention, 10-13 weeks later) and between baseline to time 2 (follow-up-3 month later))
Change in scores of the Instrumental Activities of Daily Living (IADL) scale(Change between baseline (week 0) to time 1 (post-intervention, 10-13 weeks later) and between baseline to time 2 (follow-up- 3 month later))
change in scoe of New general self efficacy scale (NGSE)(Change between baseline (week 0) to time 1 (post-intervention, 10-13 weeks later) and between baseline to time 2 (follow-up- 3 month later))
Change in scores of Patient competency rating scale (PCRS)(Change between baseline (week 0) to time 1 (post-intervention, 10-13 weeks later) and between baseline to time 2 (follow-up- 3 month later))
Change in scores Self Regulation Skills Interview (SRSI)(Change between baseline (week 0) to time 1 (post-intervention, 10-13 weeks later) and between baseline to time 2 (follow-up- 3 month later))
Change in scores of Montreal Cognitive Assessment (MoCA)(Change between baseline (week 0) to time 1 (post-intervention, 10-13 weeks later) and between baseline to time 2 (follow-up-3 month later))
Change in scores of Trail making test (TMT)(Change between baseline (week 0) to time 1 (post-intervention, 10-13 weeks later) and between baseline to time 2 (follow-up- 3 month later))
Change in scores of Dysexecutive Questionnaire (DEX)(Change between baseline (week 0) to time 1 (post-intervention, 10-13 weeks later) and between baseline to time 2 (follow-up- 3month later))
Geriatric Depression Scale - short form (GDS-SF)(Change between baseline (week 0) to time 1 (post-intervention, 10-13 weeks later) and between baseline to time 2 (follow-up- 3 month later))