RECRUITING

Investigating Dyadic Expectations About ARF Survivorship (IDEAS)

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Investigating Dyadic Expectations About ARF Survivorship (IDEAS)

Quick Facts

Study Start:2024-07-23
Study Completion:2027-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06401239

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Not specified
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * ≥18 years old
  2. * Meets study definition of ARF:
  3. * The study defines ARF as meeting 1 of the following 3:
  4. 1. Mechanical ventilation via an endotracheal tube ≥24 consecutive hours OR
  5. 2. Non-invasive ventilation (CPAP, BiPAP) ≥24 consecutive hours that is not for obstructive sleep apnea or other stable use OR
  6. 3. High flow nasal cannula with fraction of inspired oxygen (FIO2)≥.5 and flow rate ≥ litres per minute (LPM) for ≥24 consecutive hours.
  7. * Occasional rest periods of ≤1 hour are not deducted from the calculation of consecutive hours. Patients who are intubated for mental status or airway obstruction are not eligible unless they have simultaneous ARF.
  8. * Survival to hospital discharge to home
  9. * Speaks or reads English or Spanish
  10. * Identifies an adult who is expected to act as a primary care partner for at least the next 6 months.
  1. * Pre-existing cognitive impairment (IQ-CODE \>3.6)
  2. * Residing in a medical institution at hospital discharge
  3. * Receiving hospice care or life expectancy \<6 months
  4. * Homelessness or recent history of psychosis

Contacts and Locations

Study Contact

Alison E Turnbull, PhD
CONTACT
410-955-2190
turnbull@jhmi.edu
Deanna J Rahman
CONTACT
9143084938
drahman3@jh.edu

Principal Investigator

Alison E Turnbull, PhD
PRINCIPAL_INVESTIGATOR
Johns Hopkins University

Study Locations (Sites)

Johns Hopkins Hospital
Baltimore, Maryland, 21205
United States

Collaborators and Investigators

Sponsor: Johns Hopkins University

  • Alison E Turnbull, PhD, PRINCIPAL_INVESTIGATOR, Johns Hopkins University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-07-23
Study Completion Date2027-07

Study Record Updates

Study Start Date2024-07-23
Study Completion Date2027-07

Terms related to this study

Keywords Provided by Researchers

  • ARF survivor
  • Caregiver
  • ICU recovery
  • Dyadic coping
  • Dyadic self-efficacy

Additional Relevant MeSH Terms

  • Acute Respiratory Failure
  • Caregiving Stress
  • Mental Health Issue