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

Part of paid clinical trials in Baltimore, Maryland.

Sponsor
Johns Hopkins University
Study ID
NCT06341972
Status
Recruiting
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Conditions

  • Anxiety
  • Critical Illness
  • Respiratory Failure

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Cognitive behavioral therapy based self-management for anxiety — BEHAVIORAL
    Evidenced based approach for educating patients about how to manage anxiety after respiratory failure.

Study Details

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.

Key Dates

Start date
May 31, 2024
Status verified
Jun 2025
Primary completion
Feb 1, 2027
Completion
Sep 1, 2027

Study Design

Enrollment
60 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Self-management intervention
    Cognitive behavioral therapy based self-management intervention for anxiety
  • No Intervention: Usual Care
    Usual hospital-based care

Primary Outcome Measure

Treatment Satisfaction Questionnaire [ Time Frame: 5 weeks post-enrollment ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Johns Hopkins HospitalBaltimoreMaryland21287
Megan Hosey
[email protected]
410-502-2429
[email protected]
Megan Hosey, PhD (PRINCIPAL_INVESTIGATOR)

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By research site
Johns Hopkins Hospital· Baltimore, MD

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