intErnet-based iNterventions FOR Cardiac arrEst suRvivors

Not Applicable

Recruiting

• Conditions: Cognitive Impairment; Cardiac Arrest; Depression, Anxiety; Quality of Life; Social Functioning; Sexual Dysfunction

• Registration Number: NCT06395558
• Lead Sponsor: Azienda Usl di Bologna

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-4-24
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 137

Inclusion Criteria

Inclusion Criteria:<br><br> - Hospital discharge after out-of-hospital cardiac arrest with Cerebral Performance<br> Category 1 or 2<br><br> - HADS anxiety or depression = 8 and/or TICS = 31<br><br> - Informed consent for participation in the study<br><br> - Native Italian speaker or adequate understanding of the Italian language<br><br> - Adequate ability to use the web to guarantee access to the contents<br><br>Exclusion Criteria:<br><br> - Previous cognitive dysfunction<br><br> - Previous psychiatric disease<br><br> - Previous episode of out-of-hospital cardiac arrest

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Composite outcome

Secondary Outcome Measures

Name	Time	Method
HADS (Hospital Anxiety and Depression Scale) value;TICS (Telephone Interview for Cognitive Status);SF-12 (Short Form Health Survey 36);NRS (Neurobehavioural rating scale), PCRS (Patient Competency Rating Scale);NRS (Neurobehavioural rating scale);Pittsburgh Sleep Quality Index (PSQI);Sexual Interest and Satisfaction Scale (SISS);Zarit Burden Inventory (ZBI);PCRS (Patient Competency Rating Scale);HADS (Hospital Anxiety and Depression Scale) - Caregiver;PSQI (Pittsburgh Sleep Quality Index) - Caregiver;SF-12 (Short Form Health Survey 36) - Caregiver