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NCT05144477 · ClinicalTrials.gov registry record · NA

Family-Authored ICU Diaries to Reduce Fear in Patients Experiencing a Cardiac Arrest (FAID Fear)

A NA study of Cardiac Arrest and Post Traumatic Stress Syndrome, sponsored by Columbia University.

Completed
Registry status
NA
Development phase
16
Enrollment target
1
Study location

NCT05144477 is a NA study of Cardiac Arrest and Post Traumatic Stress Syndrome that has completed, run by Columbia University. The registered enrollment target is 16 participants, below the 1,479-participant average among 31 other Cardiac Arrest trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05144477, a NA study of Cardiac Arrest and Post Traumatic Stress Syndrome, has completed, sponsored by Columbia University.

COMPLETED
Registry status
NA
Development phase
16 participants
Enrollment target
1
Study location

Study Summary

The present study will: Aim 1: Enroll 15 family members of CA patients to (a) pilot recruitment procedures, (b) estimate retention, and (c) assess acceptability of study procedures. Family members will be randomized to either complete an ICU diary or to a control condition, and will complete surveys in the ICU, at patient discharge, and 30 days post-discharge. Aim 2: Obtain an estimate of the association of intervention v. control with (i) family member fear (operationalized as cardiac anxiety about the patients' cardiac condition) at hospital discharge and (ii) family member PTSS 30 days post-discharge. Exploratory Aims: Obtain an estimate of the association of intervention v. control with family member aversive cognitions towards exercise at hospital discharge.

Interventions

  • BEHAVIORAL FAID Fear Intervention

Study Locations (1)

New York

  • CUIMC - New York

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2021-11-29
Est. Completion 2022-11-30
Phase NA

Sponsor

Columbia University

958 total trials

What the Registry Record Tells You About NCT05144477

The ClinicalTrials.gov registry entry for NCT05144477 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 16 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,479-participant average among 31 other Cardiac Arrest trials with a reported enrollment target (99% lower). The listed sponsor is Columbia University, which has 958 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Cardiac Arrest appearing as the primary indexed condition, and to 1 intervention - of which FAID Fear Intervention is the first listed.

NCT05144477 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT05144477 about?

NCT05144477 is a clinical study titled "Family-Authored ICU Diaries to Reduce Fear in Patients Experiencing a Cardiac Arrest (FAID Fear)". The present study will: Aim 1: Enroll 15 family members of CA patients to (a) pilot recruitment procedures, (b) estimate retention, and (c) assess acceptability of study procedures. Family members will be randomized to either complete an ICU diary or to a control condition, and will complete surve...

What is the current status of trial NCT05144477?

This trial is currently completed. It is a NA study. The enrollment target is 16 participants. The study started on 2021-11-29. Estimated completion is 2022-11-30.

What conditions does trial NCT05144477 study?

This clinical trial studies the following conditions: Cardiac Arrest, Post Traumatic Stress Syndrome.

What interventions are being tested in trial NCT05144477?

The interventions under investigation include: FAID Fear Intervention (BEHAVIORAL).

Who is sponsoring clinical trial NCT05144477?

This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05144477 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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