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Investigating Dyadic Expectations About ARF Survivorship (IDEAS)
NCT06401239 · View on ClinicalTrials.gov ↗
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 Studied
Interventions
- OTHER Dyadic expectations about the ARF survivor's perceived health 6 months after hospital discharge
- OTHER Self-efficacy
- OTHER Concordant expectations/shared appraisal of ARF survivor's health 6 months after hospital discharge
Study Locations (1)
Maryland
- Johns Hopkins Hospital — Baltimore
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 235 participants |
| Start Date | 2024-07-23 |
| Est. Completion | 2027-07 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06401239
The ClinicalTrials.gov registry entry for NCT06401239 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 235 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins University, which has 1,517 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Mental Health Issue appearing as the primary indexed condition, and to 3 interventions — of which Dyadic expectations about the ARF survivor's perceived health 6 months after hospital discharge is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06401239 reports 1 study location spanning 1 distinct geographic area — top geographies include Maryland. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06401239 about?
NCT06401239 is a clinical study titled "Investigating Dyadic Expectations About ARF Survivorship (IDEAS)". 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 pro...
What is the current status of trial NCT06401239?
This trial is currently recruiting. The enrollment target is 235 participants. The study started on 2024-07-23. Estimated completion is 2027-07.
What conditions does trial NCT06401239 study?
This clinical trial studies the following conditions: Mental Health Issue, Acute Respiratory Failure, Caregiving Stress. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06401239?
The interventions under investigation include: Dyadic expectations about the ARF survivor's perceived health 6 months after hospital discharge (OTHER), Self-efficacy (OTHER), Concordant expectations/shared appraisal of ARF survivor's health 6 months after hospital discharge (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06401239?
This trial is sponsored by Johns Hopkins University, which has 1,517 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06401239 being conducted?
This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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