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Study of the Effect on Clinical Outcomes Using Secure Text Messaging

Study of the Effect on Clinical Outcomes Using Secure Text Messaging

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02568514
Enrollment
0
Registered
2015-10-06
Start date
2016-08-31
Completion date
2017-03-31
Last updated
2017-04-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congestive Heart Failure, Copd, Diabetes, Renal Failure

Keywords

mhealth, text messaging, secure text messaging, communication

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.

Interventions

DEVICESecure text messaging

A smartphone and web application that allows physicians and other health care professionals to communicate to each other by secure text message

Sponsors

University of Pennsylvania
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Admission to one of the hospital floors or services in the study at the Hospital of the University of Pennsylvania

Exclusion criteria

* Discharges against medical advice * Discharges to hospice

Design outcomes

Primary

MeasureTime frameDescription
Change in length of stay6 monthsChange in inpatient length of stay from baseline to 6 months
Change in 30 day hospital readmissions6 monthsChange in 30 day hospital readmissions from baseline to 6 months
Change in inpatient mortality6 monthsChange in inpatient mortality from baseline to 6 months

Secondary

MeasureTime frameDescription
Change in Hospital Consumer Assessment of Healthcare Providers and Systems (HCAPs) scores6 monthsChange in HCAP scores from baseline to 6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026