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Clinical Trials/NCT01671189
NCT01671189
Unknown
Early Phase 1

An Automated SMS-Based Reminder and Rescheduling Tool to Improve Appointment Adherence Rates and Glycemic Control Among Diabetes Patients in San Mateo County

Medic Mobile1 site in 1 country300 target enrollmentOctober 2012

Overview

Phase
Early Phase 1
Intervention
Not specified
Conditions
Diabetes Mellitus Type 2
Sponsor
Medic Mobile
Enrollment
300
Locations
1
Primary Endpoint
Glycemic Control (hemoglobin A1c)
Last Updated
13 years ago

Overview

Brief Summary

Medic Mobile conceptualized and proposed the creation of an SMS-based appointment validation tool to automate appointment confirmation and rescheduling. Working in parallel with the San Mateo Medical Center (SMMC) electronic medical records (EMR) system, the software tool will automate reminders that request text responses from patients to either confirm or request to reschedule their upcoming appointments. While simple in concept, this tool aims to free up scarce clinical resources which are currently allocated to daily patient phone call reminders. With funding from a Bay Area foundation, the investigators will develop and pilot this open-source software tool in a 12-month randomized-controlled trial, slated to begin in October 2012. The endpoints of the study will aim to demonstrate improvements in both appointment adherence and glycemic control.

Registry
clinicaltrials.gov
Start Date
October 2012
End Date
December 2013
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Medic Mobile
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Belong to Willow Clinic or Fair Oaks Clinic under the San Mateo Medical Center
  • Have a diagnosis of type 2 diabetes as indicated by ICD-9 code of 249.xx or 250.xx
  • Have a most recent hemoglobin A1c (HbA1c) level greater than 7%
  • Are at least 18 years of age
  • Have access to cell phone
  • Are literate or live with a friend/family member who is literate and willing to handle associated text messages

Exclusion Criteria

  • Have a terminal illness and prognosis of less than one year
  • Are unable to demonstrate the ability to reply to an SMS and lack an appropriate proxy
  • Are pregnant or expect to be pregnant in the next 6-9 months

Outcomes

Primary Outcomes

Glycemic Control (hemoglobin A1c)

Time Frame: 6-9 months post-enrollment

The hemoglobin A1c (HbA1c) levels of study participants will be measured at the time of enrollment and at the end of the 6-9 month follow-up period.

Secondary Outcomes

  • Appointment Adherence Rate(6-9 month post-enrollment)

Study Sites (1)

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