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ENROLLING BY INVITATION
NCT07240714
NA

Effects of a Web-based Support Programme for Cardiac Arrest Survivors

Sponsor: Linkoeping University

View on ClinicalTrials.gov

Summary

The overall goal of this clinical trial is to learn if a web-based support programme can improve wellbeing in cardiac arrest survivors by helping them manage emotional, cognitive, and physical challenges. The study also explores how the programme is used and experienced in practice. The main questions it aims to answer are: * Can access to a web-based support programme improve overall wellbeing in cardiac arrest survivors? * Can it also enhance quality of life, cognitive function, life satisfaction, and sleep, while reducing anxiety, depression, post-traumatic stress, and fatigue? Researchers will compare cardiac arrest survivors who receive a web-based support programme in addition to standard care with those who receive standard care alone, to see if the programme improves wellbeing and other health outcomes. After the study, the control group will also gain access to the programme. Participants will: * Be asked to complete online questionnaires at three time points: at the start of the study, after 3 months, and after 6 months. * Be encouraged to use a web-based support programme for 3 months, with unlimited access, at their own pace and according to their individual needs (intervention group only).

Official title: Effects of a Web-based Support Programme for Cardiac Arrest Survivors: A Randomized Controlled Trial With Process Evaluation (The CARDIS Study)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

120

Start Date

2025-11-20

Completion Date

2028-08-31

Last Updated

2026-08-26

Healthy Volunteers

No

Interventions

BEHAVIORAL

Digital Support Programme

The intervention consists of a web-based support programme designed for individuals recovering from cardiac arrest. Participants in the intervention group receive access to the programme for 12 weeks. The programme includes educational modules, patient and family stories, videos, practical exercises (e.g., breathing techniques, fatigue management), tools for personal recovery planning, and a moderated chat forum for peer support. Participants can access the content at their own pace and according to their individual needs. The programme is delivered entirely online and does not require any physical visits or clinical procedures.

Locations (9)

Sahlgrenska Universitetssjukhuset

Gothenburg, Sweden

Östra sjukhuset

Gothenburg, Sweden

Helsingborgs lasarett

Helsingborg, Sweden

Länssjukhuset

Kalmar, Sweden

Universitetssjukhuset

Linköping, Sweden

Skånes universitetssjukhus

Lund, Sweden

Lasarettet i Motala

Motala, Sweden

Vrinnevisjukhuset

Norrköping, Sweden

Västmanlands sjukhus Västerås

Västerås, Sweden