WithdrawnNot Applicable

Electronic Health Record-Integrated Patient-Generated Data

Stopped: protocol changes were made and study no longer a clinical trial

0Started 2026-04

Plain-language summary

The purpose of this study is to find out if patients that receive supportive messaging with response adaptation are more likely to adhere to patient-generated data collection and electronic health record integration, compared to patients that do not receive supportive messaging.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Discharged alive from the hospital without hospice care who meet clinical criteria for infection and organ dysfunction consistent with sepsis * Enrolled into the Sepsis Transition and Recovery program * Enrolled or willing to enroll as an Epic MyChart user Exclusion Criteria: * Discharged from the hospital with hospice care

What they're measuring

Proportion of Completed Versus Requested Patient-Generated Data

Timeframe: 90 days post hospital discharge

Trial details

NCT IDNCT06668870

SponsorWake Forest University Health Sciences

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-10

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