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Investigating Dyadic Expectations About ARF Survivorship (IDEAS)

NCT06401239 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 235

Last updated 2026-02-05

No results posted yet for this study

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.

Conditions

  • Acute Respiratory Failure
  • Caregiving Stress
  • Mental Health Issue

Interventions

OTHER

Dyadic expectations about the ARF survivor's perceived health 6 months after hospital discharge

Dyad members' expectations will be collected at baseline and at 3- month follow-up assessments using a visual analogue scale (VAS) ranging from 0 - 100, similar to the EQ-5D-VAS.

OTHER

Self-efficacy

Self-efficacy in both dyad members will be assessed at 3- and 6-month follow-up assessments using the Generalized Self-Efficacy Scale (GSE). The GSE has 10 items scored on a 4-point scale. U.S. adult population norms are available.

OTHER

Concordant expectations/shared appraisal of ARF survivor's health 6 months after hospital discharge

Dyad members' expectations will be collected at baseline and at 3- month follow-up assessments using a visual analogue scale (VAS) ranging from 0 - 100, similar to the EQ-5D-VAS.

Sponsors & Collaborators

Principal Investigators

  • Ann M Parker, MD, PhD · Johns Hopkins University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-07-23
Primary Completion
2027-07-31
Completion
2027-07-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06401239 on ClinicalTrials.gov