Image

Investigating Dyadic Expectations About ARF Survivorship (IDEAS)

Investigating Dyadic Expectations About ARF Survivorship (IDEAS)

Recruiting
18 years and older
All
Phase N/A

Powered by AI

Overview

The purpose of this observational study is to understand how adults who survive acute respiratory failure (ARF) and the people (usually family) who support ARF survivors after returning home think about the first 6 months of recovery. The study aims to find out if expectations about the recovery process after ARF are associated with mental health symptoms in both survivors and the survivor's care partners. Study participants will complete 3 surveys over 6 months. These surveys ask questions about participants' future expectations, feelings, and mood. Surveys can be completed online, over the phone, or on paper.

Description

The overarching objectives of the Investigating Dyadic Expectations about ARF Survivorship (IDEAS) cohort study are to learn how expectations about ARF survivorship are related to dyadic mental health symptoms and dyadic coping. Specifically, the study aims are:

  • Aim 1: To determine whether health expectations and self-efficacy after acute respiratory failure (ARF) are associated with mental health outcomes in survivor-care partner dyads.
  • Aim 2: To assess whether concordant expectations within survivor-care partner dyads are associated with better dyadic coping (primary outcome) and exploratory secondary outcomes.

The term dyadic coping refers to the ways two people interact as the pair manage illness-related stressors. Concordant expectations within dyads, also called shared appraisal, refers to both members of a dyad being "on the same page", and is hypothesized to lead to better dyadic coping behaviors.

Eligibility

Patient Inclusion Criteria:

  • ≥18 years old
  • Meets study definition of ARF:
    • The study defines ARF as meeting 1 of the following 3:
      1. Mechanical ventilation via an endotracheal tube ≥24 consecutive hours OR
      2. Non-invasive ventilation (CPAP, BiPAP) ≥24 consecutive hours that is not for obstructive sleep apnea or other stable use OR
      3. High flow nasal cannula with fraction of inspired oxygen (FIO2)≥.5 and flow rate ≥ litres per minute (LPM) for ≥24 consecutive hours.
    • Occasional rest periods of ≤1 hour are not deducted from the calculation of

      consecutive hours. Patients who are intubated for mental status or airway obstruction are not eligible unless they have simultaneous ARF.

  • Survival to hospital discharge to home
  • Speaks or reads English or Spanish
  • Identifies an adult who is expected to act as a primary care partner for at least the next 6 months.

Patient Exclusion Criteria:

  • Pre-existing cognitive impairment (IQ-CODE >3.6)
  • Residing in a medical institution at hospital discharge
  • Receiving hospice care or life expectancy <6 months
  • Homelessness or recent history of psychosis

Care Partner Inclusion Criteria:

  • ≥18 years old
  • Speaks or reads English or Spanish

Care Partner Exclusion Criteria:

  • Pre-existing cognitive impairment (IQ-CODE >3.6)

Study details
    Acute Respiratory Failure
    Caregiving Stress
    Mental Health Issue

NCT06401239

Johns Hopkins University

28 July 2025

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.