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

Johns Hopkins University
NCT IDNCT06341972ClinicalTrials.gov data as of Apr 2026
Target enrollment

60

Study length

about 3.3 years

Ages

18+

Locations

1 site in MD

About this study

Researchers are testing if a self-management intervention can help reduce anxiety in people who have survived acute respiratory failure. The trial will compare this new approach to usual care, and see if it helps lower anxiety symptoms at the end of the treatment and after 3 months.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Participate in Cognitive behavioral therapy based self-management for anxiety

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low6%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Secondary: Healthcare Utilization as assessed by Healthcare Utilization interview, Hospital Anxiety and Depression Scale, Montreal Cognitive Assessment - Blind, Quality of Life as assessed by the European Quality of Life Scale (EQ-5D), Visual Analog Scale - Anxiety

Body systems

Psychiatry / Mental Health