New website aims to ease fear for families after cardiac arrest
NCT ID NCT06048068
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a website called Heartsight could help close family members of cardiac arrest patients feel less uncertain, anxious, and burdened. Fifty-three family members were given access to the website or usual care. The goal was to see if the website was easy to use and helpful in reducing emotional distress three months after the patient left the hospital.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Heartsight website (educational informational platform)
- What this could lead to
- If it works, this could provide a simple, low-cost tool to help families cope with the emotional aftermath of a loved one's cardiac arrest.
- What could go wrong
- This is a small pilot study with only 53 participants, so results may not apply to everyone. The website may not significantly reduce distress compared to usual care.
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
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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
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53 people
The number who actually took part.
- Started
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Sep 2023
- Finished
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Oct 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * 18 years of age or older * Surrogate of a living NewYork Presbyterian Hospital cardiac arrest patient * English- or Spanish-speaking * Has a working smartphone, tablet, laptop, or other device with internet access Exclusion Criteria: * Any medical and/or psychiatric impairment precluding them from complying with the protocol * Non-English and non-Spanish speaking * Lack of internet/device access * Surrogate of an adult CA patient who passed away * Cannot be reached for initial contact (3 unsuccessful attempts made in ICU) * Moved to the in-patient floor before initial contact can be established
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Columbia University Medical Center/New York Presbyterian
New York, New York, 10032, United States
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Other studies related to the condition(s) this trial covers.
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