NCT Number: NCT02453074
Automated System for Gathering and Reporting Clinical Outcomes to Providers
The purpose of this study is to design and test the feasibility of a system to survey patients regarding the outcome of acute care visits and to report back to the healthcare providers.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Adults age 18 and older visiting participating primary care clinics who agree to be contacted by email to complete a survey on clinical outcomes.
Exclusion criteria
- None
Treatment and study plan
Primary outcomes
-
Survey response rate
Time frame: Assessed at the end of the 12 week study period
Sponsors and collaborators
Lead sponsor
Harvard Medical School (HMS and HSDM)
Other
Registry information
Important dates
- Study start
- 2015
- Primary completion
- 2015
- Study completion
- 2015
- First posted
- May 25, 2015
- Registry last updated
- May 25, 2015
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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