Effectiveness of FACoT for Individuals Post Stroke

Not Applicable

Completed

• Conditions: Stroke

• Registration Number: NCT02925637
• Lead Sponsor: Bait Balev Hospital

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2016-08-03
• Study First Submitted QC: 2016-10-05
• Study First Posted: 2016-10-06
• Study Start: 2017-03-12
• Status Verified: 2019-02
• Primary Completion: 2020-02-27
• Study Completion: 2020-02-27
• Last Update Submitted: 2021-04-11
• Last Update Posted: 2021-04-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 66

Inclusion Criteria

Not provided

Exclusion Criteria

• with no other neurological or psychiatric conditions
• without dementia

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Change in scores of The Canadian Occupational Performance Measure (COPM)	Change between baseline (week 0) to time 1 (post-intervention -10-13 weeks later) and time 2 (follow-up- three month later)

Secondary Outcome Measures

Name	Time	Method
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)

Trial Locations

Locations (1)

Maccabi; 🇮🇱 Ashdod, Israel