A Study to Evaluate Jaspr Application Compared to Care As Usual (CAU) in Emergency Department
Overview
Tab Title Description
Study type
InterventionalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Rochester, Minnesota: 19-010319
Sponsor Protocol Number: 19-010319
About this study
The purpose of this study is to compare Jaspr to Care-as-Usual (CAU) in Emergency departments nationwide.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:
- Currently in the ED seeking treatment for suicidal behavior.
- Medically and clinically stable, as deemed by ED medical personnel/patient’s care team.
- Access to a computer or other device (smartphone, tablet) with Internet connection.
- Currently has and regularly uses an Apple or Android smartphone.
- Stable address and housing for the last 30 days.
Exclusion Criteria:
- Acutely psychotic, severely agitated, and patients with significant intoxication or other impairment (as deemed by medical providers) that may interfere with providing consent and meaningful feedback (as determined by their care team).
- No access or way to access phone or computer (or other device) with Internet connection.
- homeless or unstable housing in the past 30 days.
- Severely agitated patients are those who are perceived by medical personnel as highly distressed and likely to become more agitated (e.g., yelling, throwing objects, engaging in self-harming behaviors) and/or distressed if approached by medical personnel and/or research staff about research-related activities, from inquiring about their interest to participate and obtaining informed consent to providing feedback to researchers.
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
More information
Publications
Publications are currently not available