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Study identifier: NCT06341972 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Respiratory Failure · Anxiety · Critical Illness  ·  Sponsor: Johns Hopkins University

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

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? * Is this intervention in the ICU and hospital associated with reduced anxiety symptoms? Participants will participate in a cognitive behavioral therapy informed self-management intervention aimed to reduce anxiety symptoms. Researchers will compare the intervention group to patients who receive usual care to see if the intervention reduces symptoms at the the conclusion of the intervention and at 3 months follow-up.

This description comes directly from the study's public registry record.

Talk to the study team

Megan Hosey, PhD  ·  410-502-2429  ·  mhosey@jhu.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Johns Hopkins HospitalBaltimore, Maryland, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06341972