A Mobile Personal Health Record for Behavioral Health Homes (mPHR)

This study is not yet open for participant recruitment.
Verified November 2013 by Emory University
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Benjamin Druss, Emory University
ClinicalTrials.gov Identifier:
NCT01890226
First received: June 25, 2013
Last updated: November 18, 2013
Last verified: November 2013

June 25, 2013
November 18, 2013
July 2013
December 2017   (final data collection date for primary outcome measure)
Quality of General Medical Care [ Time Frame: 1 year ] [ Designated as safety issue: No ]
Quality of preventive medical services as measured by proportion of indicated US Preventive Services Taskforce Recommendations received Quality of cardiometabolic care as measured by proportion of indicated RAND quality measures for diabetes, hypertension and hypercholesterolemia received
Same as current
Complete list of historical versions of study NCT01890226 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
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A Mobile Personal Health Record for Behavioral Health Homes
A Mobile Personal Health Record for Behavioral Health Homes

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.

Not Provided
Interventional
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Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Health Services Research
  • Hypertension
  • Hyperlipidemia
  • Diabetes
Behavioral: Mobile Personal Health Record App.
  • No Intervention: Control
  • Experimental: Experimental: Intervention
    Participants randomized to the intervention arm will receive the mobile personal health record.
    Intervention: Behavioral: Mobile Personal Health Record App.
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Not yet recruiting
300
June 2018
December 2017   (final data collection date for primary outcome measure)

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
Both
18 Years and older
No
Contact: Gretl Glick 404-712-8529 gglick@emory.edu
Contact: Silke von Esenwein, Ph.D 404-712-8525 svonese@emory.edu
United States
 
NCT01890226
IRB00067447, 1R01MH100467 - 01
Yes
Benjamin Druss, Emory University
Emory University
National Institute of Mental Health (NIMH)
Principal Investigator: Benjamin Druss, MD, MPH Emory University
Emory University
November 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP