[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100546920":3},{"organization":4,"armGroups":7,"interventions":16,"overallOfficials":28,"centralContacts":32,"locations":41,"responsibleParty":59,"collaborators":61,"id":65,"slug":66,"hasResults":67,"nctId":68,"briefTitle":69,"officialTitle":69,"acronym":70,"eligibilityCriteria":71,"healthyVolunteers":67,"sex":72,"minAge":73,"maxAge":10,"enrollmentInfo":74,"targetDuration":10,"studyType":77,"phases":10,"briefSummary":78,"conditions":79,"keywords":83,"overallStatus":44,"whyStopped":10,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":98},{"fullName":5,"class":6},"Johns Hopkins University","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"ARF Survivor-Care Partner Dyads",null,"The study will recruit 235 dyads of adult ARF survivors and care partners. The term \"care partner\" refers to an individual (e.g. family member or friend) that supports the survivor at home.",[13,14,15],"Other: Dyadic expectations about the ARF survivor's perceived health 6 months after hospital discharge","Other: Self-efficacy","Other: Concordant expectations\u002Fshared appraisal of ARF survivor's health 6 months after hospital discharge",[17,21,25],{"type":6,"name":18,"description":19,"armGroupLabels":20,"otherNames":10},"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.",[9],{"type":6,"name":22,"description":23,"armGroupLabels":24,"otherNames":10},"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.",[9],{"type":6,"name":26,"description":19,"armGroupLabels":27,"otherNames":10},"Concordant expectations\u002Fshared appraisal of ARF survivor's health 6 months after hospital discharge",[9],[29],{"name":30,"affiliation":5,"role":31},"Ann M Parker, MD, PhD","PRINCIPAL_INVESTIGATOR",[33,37],{"name":30,"role":34,"phone":35,"phoneExt":10,"email":36},"CONTACT","410-955-2190","ann.parker@jhmi.edu",{"name":38,"role":34,"phone":39,"phoneExt":10,"email":40},"Omar R Valentin","410-502-2140","ovalent1@jh.edu",[42],{"facility":43,"status":44,"city":45,"state":46,"zip":47,"country":48,"countryCode":49,"cosmosGeoPoint":50,"geoPoint":55,"contacts":56},"Johns Hopkins Hospital","RECRUITING","Baltimore","Maryland","21205","United States","US",{"type":51,"coordinates":52},"Point",[53,54],-76.61219,39.29038,{"lat":54,"lon":53},[57,58],{"name":30,"role":34,"phone":35,"phoneExt":10,"email":36},{"name":38,"role":34,"phone":10,"phoneExt":10,"email":40},{"type":60,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[62],{"name":63,"class":64},"National Heart, Lung, and Blood Institute (NHLBI)","NIH","100546920","investigating-dyadic-expectations-about-arf-survivorship-ideas-100546920",false,"NCT06401239","Investigating Dyadic Expectations About ARF Survivorship (IDEAS)","IDEAS","Patient Inclusion Criteria:\n\n* ≥18 years old\n* Meets study definition of ARF:\n\n  * The study defines ARF as meeting 1 of the following 3:\n\n    1. Mechanical ventilation via an endotracheal tube ≥24 consecutive hours OR\n    2. Non-invasive ventilation (CPAP, BiPAP) ≥24 consecutive hours that is not for obstructive sleep apnea or other stable use OR\n    3. High flow nasal cannula with fraction of inspired oxygen (FIO2)≥.5 and flow rate ≥ litres per minute (LPM) for ≥24 consecutive hours.\n  * 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.\n* Survival to hospital discharge to home\n* Speaks or reads English or Spanish\n* Identifies an adult who is expected to act as a primary care partner for at least the next 6 months.\n\nPatient Exclusion Criteria:\n\n* Pre-existing cognitive impairment (IQ-CODE \\>3.6)\n* Residing in a medical institution at hospital discharge\n* Receiving hospice care or life expectancy \\\u003C6 months\n* Homelessness or recent history of psychosis\n\nCare Partner Inclusion Criteria:\n\n* ≥18 years old\n* Speaks or reads English or Spanish\n\nCare Partner Exclusion Criteria:\n\n* Pre-existing cognitive impairment (IQ-CODE \\>3.6)","ALL","18 Years",{"count":75,"type":76},235,"ESTIMATED","OBSERVATIONAL","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.",[80,81,82],"Acute Respiratory Failure","Caregiving Stress","Mental Health Issue",[84,85,86,87,88],"ARF survivor","Caregiver","ICU recovery","Dyadic coping","Dyadic self-efficacy","2026-02-03",{"date":91,"type":92},"2026-02-05","ACTUAL",{"date":94,"type":92},"2024-07-23",{"date":96,"type":76},"2027-07",{"name":5,"class":6},1]