Life sciences · Interventional Study
ClinicalTrials.gov · November 5, 2026
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Interventional Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT07778004). This is a study registration, not published results. Lead sponsor: University of North Carolina, Chapel Hill. Recruitment status: NOT_YET_RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 144 participants (ESTIMATED). Conditions: Acute Respiratory Failure, Critical Illness, Sepsis, Hypoxia, Hypercapnia. Interventions: BEHAVIORAL: ICU-SUCCEED; OTHER: Augmented Usual Care. Primary outcome measures: Feasibility of participant eligibility , From the start to the end of recruitment; Feasibility of recruitment , From the start to the end of recruitment; Feasibility of enrollment , From the start to end of recruitment; Feasibility of ICU-SUCCEED inpatient session , From recruitment start to inpatient session completion; Feasibility of intervention completion , From enrollment through intervention completion, average of 8 weeks; Feasibility of retention , From enrollment to day 90 follow-up; Intervention acceptability , Day 90. Brief summary: This study will investigate whether a family-centered intervention that has been adapted for patients with critical illness and their caregivers is possible, acceptable, and helpful