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Diary kept by nurses may ease trauma after sudden death

NCT ID NCT02874469

Knowledge-focused Sponsor: University Hospital, Lille Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at whether keeping a diary during intensive care can lower the risk of post-traumatic stress disorder (PTSD) in people who survived a sudden cardiac arrest and in their family members. About 173 patients and their relatives took part. Researchers measured PTSD symptoms three months after the event to see if the diary helped.

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

173 people

The number who actually took part.

Started

Dec 2014

Finished

Dec 2023

Lead sponsor

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

18 years and older

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 = * Patients who experienced a sudden death and who are admitted alive in our center * Patients who benefited from therapeutic hypothermia (and/or care to limit fever occurrence) Relative's inclusion criteria : * Relatives of a patient that fit inclusion/exclusion criteria Exclusion Criteria = Patient's non-inclusion criteria : * Death or transfer in another center within the first 8 hours of admission in our center * Pregnancy * Patients who refuse to participate after being awake after initial coma Relative's non-inclusion criteria : * Relatives who refuse to participate after being awake after initial coma

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Conditions

The condition(s) this trial relates to.

Death, Sudden Death, Sudden, Cardiac post-traumatic stress disorder sudden cardiac arrest

As listed by the trial registrant

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

Sudden cardiac arrest Sudden death

Contacts and locations

Locations

  • Hôpital Cardiologique - USIC - CHRU

    Lille, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.