Patient Outcomes Reporting for Timely Assessments of Life With Depression: PORTAL-Depression
Completed · Not applicable
Conditions studied: Depression, Depressive Disorder, Major
In brief
Currently, very little research exists on whether patient portals could be used to integrate patient-reported outcome (PRO) measurement into the electronic health record (EHR) and clinical practice, even though 87% of ambulatory care practices have EHRs and 88% of U.S. adults have access to the internet. To date, no randomized controlled trial has examined whether patient portals can be used to collect PRO measures. The goal of this study is to implement the integration of a computerized adaptive test (CAT) for patient-reported outcome (PRO) measurement of depression symptoms into an electronic health record (EHR) and evaluate the effectiveness of collecting CAT PROs via an EHR patient portal in two randomized controlled trials. This study will advance the science of implementation of patient-centered outcomes research into clinical practice, as well as the evidence for high quality, accessible care.
Key facts
- Study ID
- NCT03832283
- Run by
- University of Chicago
- People needed
- 4161
- Starts
- 2019-05-01
- Expected to finish
- 2021-03-01
- Last updated by the study team
- 2021-04-30
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 18 years or older
- considered an active clinic patient at the start date of the intervention
- have an active MyChart account that is not managed by a proxy
- receive care from a participating PCP
- due for depression screening (screening arms) or active depression (monitoring arms)
You may not qualify if…
- under 18 years of age
- bipolar disorder
Where it is running
- University of Chicago — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
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