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Clinical Trials/NCT01890226
NCT01890226
Completed
Not Applicable

A Mobile Personal Health Record for Behavioral Health Homes

Emory University1 site in 1 country311 target enrollmentNovember 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
Emory University
Enrollment
311
Locations
1
Primary Endpoint
Change in Composite Quality Score
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Poor quality of medical care is a major contributor to excess medical morbidity and premature mortality in persons with serious mental illnesses (SMI). To address this problem, community mental health providers are increasingly partnering with safety net medical providers to develop behavioral health homes, integrated clinics in which persons with SMI receive coordinated medical and mental health care. However, behavioral health homes have faced logistical and privacy challenges in integrating electronic medical records across organizations.

This application proposes to develop and test a mobile Personal Health Record (mPHR) to overcome this problem while more fully engaging patients in their health care. The study will develop, test, and disseminate the mPHR. The investigators will develop the app building on experience and preliminary data from a PC-based PHR project, and link it to the medical and mental health EHR in a behavioral health home. Next, the investigators will conduct a randomized trial of the mPHR in 300 subjects randomized to the mPHR or usual care.

Registry
clinicaltrials.gov
Start Date
November 2014
End Date
January 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Benjamin Druss

Professor

Emory University

Eligibility Criteria

Inclusion Criteria

  • one or more of the following conditions: hyperlipidemia, hypertension, diabetes
  • able to give consent
  • patient in the behavioral health home

Exclusion Criteria

  • Unable to give consent

Outcomes

Primary Outcomes

Change in Composite Quality Score

Time Frame: Baseline, 12 month post intervention

It is a measure of quality of care. The aggregate score represents the total number of eligible services received for an individual generated by dividing all instances in which recommended care was delivered by the number of times a participant was eligible for the indicator. The score ranges from 0 to 1 with higher scores indicating receipt of recommended care/services.

Secondary Outcomes

  • Change in Health-related Quality of Life(Baseline, 6 month post intervention, 12 month post intervention)
  • Change in Patient Activation Measure(Baseline, 6 month post intervention, 12 month post intervention)
  • Change in Patient Assessment of Chronic Illness Care(Baseline, 6 month post intervention, 12 month post intervention)

Study Sites (1)

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