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Web app aims to boost heart attack survivors' mental health

NCT ID NCT06395558

Symptom relief Sponsor: Azienda Usl di Bologna Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a web-based program can improve quality of life for people who survived a cardiac arrest outside the hospital. The program includes educational sessions, brain games, and tips on physical activity and nutrition. Researchers will enroll 106 survivors and measure changes in anxiety, depression, thinking skills, and social functioning.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Multimodal web-based intervention (knowledge sessions, games, physical activity and nutrition guidance)
What this could lead to
If it works, this could offer a convenient, home-based way to help cardiac arrest survivors feel better emotionally and mentally.
What could go wrong
This is a small, early-stage trial with only 106 participants, so results may not apply to everyone. The program requires internet access and computer skills, which could limit who can benefit.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 106 people

The number the study aims to enrol. It can still change while the study runs.

Started

Aug 2024

Expected to finish

Oct 2027

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 80 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

anxiety disorder cardiac arrest Cognitive Dysfunction Depression physiological sexual disorder Social Adjustment

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Cardiac arrest Cognitive impairment Depression, anxiety Quality of life Sexual dysfunction Social functioning

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Azienda Unità Sanitaria Locale

    RECRUITING

    Bologna, Bologna, 40100, Italy

  • Montecatone Rehabilitation Institute

    RECRUITING

    Imola, Bologna, 40026, Italy

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