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Improving Psychological Outcomes for Acute Respiratory Failure Survivors Using a Self-Management Intervention

NCT06341972

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

A growing number of patients are surviving a stay in the intensive care unit (ICU) but may experience long-lasting psychological problems, but research evaluating such treatment for ICU patients is scant. The goal of this pilot randomized controlled trial is to evaluate the feasibility, acceptability, and potential benefit of an evidence-based psychological intervention for anxiety and associated outcomes for ICU patients. The main question[s] it aims to answer are: Is this intervention feasible and acceptable in ARF patients?

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Respiratory Failure
  • Anxiety
  • Critical Illness

Eligibility basics and study details

Study type
Interventional
Phase
Not applicable
Ages
18 years and older
Sex
All
Healthy volunteers
Accepted
Sponsor
Johns Hopkins University
Last updated on ClinicalTrials.gov
June 22, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Maryland · 1

  • Johns Hopkins Hospital · Baltimore, MD

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.