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Life sciences · Interventional Study
ClinicalTrials.gov · October 26, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
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 (NCT04829188). This is a study registration, not published results. Lead sponsor: University of Pittsburgh. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 1296 participants (ACTUAL). Conditions: Sepsis, Pneumonia, Lower Resp Tract Infection, Covid19. Interventions: BEHAVIORAL: Structured Telephone Support (STS); BEHAVIORAL: Low-intensity Remote Patient Monitoring (RPM-Low); BEHAVIORAL: High-intensity Remote Patient Monitoring (RPM-High); BEHAVIORAL: Standard Response Team; BEHAVIORAL: Enhanced Response Team. Primary outcome measures: Post-discharge Home Days , 90 days after discharge to home. Brief summary: An adaptive platform trial to compare effectiveness of different care models to prevent readmissions for patients hospitalized with sepsis or lower respiratory tract infection. The primary outcome is number of days spent at home within 90 days after hospital discharge.