Study of the Effect on Clinical Outcomes Using Secure Text Messaging
- Conditions
- Congestive Heart FailureRenal FailureCopdDiabetes
- 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- WITHDRAWN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
- Admission to one of the hospital floors or services in the study at the Hospital of the University of Pennsylvania
- Discharges against medical advice
- Discharges to hospice
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Secure text messaging Secure text messaging Patients 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
Name Time Method Change in 30 day hospital readmissions 6 months Change in 30 day hospital readmissions from baseline to 6 months
Change in length of stay 6 months Change in inpatient length of stay from baseline to 6 months
Change in inpatient mortality 6 months Change in inpatient mortality from baseline to 6 months
- Secondary Outcome Measures
Name Time Method Change in Hospital Consumer Assessment of Healthcare Providers and Systems (HCAPs) scores 6 months Change in HCAP scores from baseline to 6 months
Trial Locations
- Locations (1)
University of Pennsylvania
🇺🇸Philadelphia, Pennsylvania, United States