RecruitingNot Applicable

Investigating Dyadic Expectations About ARF Survivorship (IDEAS)

United States235 participantsStarted 2024-07-23

Plain-language summary

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.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Mechanical ventilation via an endotracheal tube ≥24 consecutive hours OR
✓. Non-invasive ventilation (CPAP, BiPAP) ≥24 consecutive hours that is not for obstructive sleep apnea or other stable use OR
✓. High flow nasal cannula with fraction of inspired oxygen (FIO2)≥.5 and flow rate ≥ litres per minute (LPM) for ≥24 consecutive hours.

What they're measuring

Symptoms of Anxiety and Depression as Assessed by the Hospital Anxiety and Depression Scale (HADS)

Timeframe: 3 and 6 months after ARF survivor's ICU discharge

Dyadic Coping as Assessed by the Dyadic Coping Inventory (DCI)

Timeframe: 3 and 6 months after ARF survivor's ICU discharge

Trial details

NCT IDNCT06401239

SponsorJohns Hopkins University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2027-07

Contact for this trial

Ann M Parker, MD, PhD

410-955-2190 ann.parker@jhmi.edu

View on ClinicalTrials.gov More Acute Respiratory Failure trials