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Study of the Effect on Clinical Outcomes Using Secure Text Messaging

Not Applicable
Withdrawn
Conditions
Congestive Heart Failure
Renal Failure
Copd
Diabetes
Interventions
Device: Secure text messaging
Registration Number
NCT02568514
Lead Sponsor
University of Pennsylvania
Brief Summary

In this study, the investigators will conduct a randomized, controlled trial to evaluate the impact of offering mobile secure text messaging on clinical outcomes.

Detailed Description

Inpatient health care providers such as physicians and nurses spend up to one-third of their time communicating with other health care providers. Many of these communications have shifted mediums from handwritten notes and face-to-face conversations to phone calls and paging systems. More recently the rapid adoption of smartphones has led to the use of mobile-enabled technologies using smartphones such as text messaging and email. While these technologies may offer ease and fit better within the clinical workflow, they often send patient information through unsecure cellular or internet connections. Mobile secure text messaging may address these issues by encrypting data and allowing for asynchronous or synchronous communication between individual providers or groups of providers. In this study, the investigators will conduct a randomized, controlled trial to evaluate the impact of offering mobile secure text messaging on clinical outcomes.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Admission to one of the hospital floors or services in the study at the Hospital of the University of Pennsylvania
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Exclusion Criteria
  • Discharges against medical advice
  • Discharges to hospice
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Secure text messagingSecure text messagingPatients admitted to hospital floors on which physicians and other staff are able to communicate with each other (not to the patient) using mobile secure text messaging.
Primary Outcome Measures
NameTimeMethod
Change in 30 day hospital readmissions6 months

Change in 30 day hospital readmissions from baseline to 6 months

Change in length of stay6 months

Change in inpatient length of stay from baseline to 6 months

Change in inpatient mortality6 months

Change in inpatient mortality from baseline to 6 months

Secondary Outcome Measures
NameTimeMethod
Change in Hospital Consumer Assessment of Healthcare Providers and Systems (HCAPs) scores6 months

Change in HCAP scores from baseline to 6 months

Trial Locations

Locations (1)

University of Pennsylvania

🇺🇸

Philadelphia, Pennsylvania, United States

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