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Recruiting NCT06395558

NCT06395558 intErnet-based iNterventions FOR Cardiac arrEst suRvivors

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Clinical Trial Summary
NCT ID NCT06395558
Status Recruiting
Phase
Sponsor Azienda Usl di Bologna
Condition Cognitive Impairment
Study Type INTERVENTIONAL
Enrollment 106 participants
Start Date 2024-08-05
Primary Completion 2027-08-05

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
Lifestyle intervention

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 106 participants in total. It began in 2024-08-05 with a primary completion date of 2027-08-05.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This randomized clinical trial will test whether an internet-based lifestyle intervention administered through a web app can foster Health Related Quality of Life in patients who survived an out-of-hospital cardiac arrest and suffer from these symptoms

Eligibility Criteria

Inclusion Criteria: * Hospital discharge after out-of-hospital cardiac arrest with Cerebral Performance Category 1 or 2 * Informed consent for participation in the study * Native Italian speaker or adequate understanding of the Italian language * Adequate ability to use the web to guarantee access to the contents Exclusion Criteria: * Previous cognitive dysfunction * Previous psychiatric disease * Previous episode of out-of-hospital cardiac arrest

Contact & Investigator

Central Contact

Lorenzo Gamberini, MD

✉ gamberini6@ausl.bologna.it

📞 3403550540

Principal Investigator

Lorenzo Gamberini, MD

PRINCIPAL INVESTIGATOR

Azienda USL Bologna

Frequently Asked Questions

Who can join the NCT06395558 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Cognitive Impairment. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06395558 currently recruiting?

Yes, NCT06395558 is actively recruiting participants. Contact the research team at gamberini6@ausl.bologna.it for enrollment information.

Where is the NCT06395558 trial being conducted?

This trial is being conducted at Bologna, Italy, Imola, Italy.

Who is sponsoring the NCT06395558 clinical trial?

NCT06395558 is sponsored by Azienda Usl di Bologna. The principal investigator is Lorenzo Gamberini, MD at Azienda USL Bologna. The trial plans to enroll 106 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology