Promoting Improved Functioning Among People Experiencing Stressful Situations

Recruiting N/A Interventional Study
Acute Stress Reaction
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 50
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
450 (estimated)
Sponsor
University of North Carolina, Chapel Hill · Other
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About This Trial
The iCOVER intervention was developed to rapidly restore functioning in individuals experiencing an Acute Stress Reaction (ASR). iCOVER is undergoing widespread adoption but has not been tested for efficacy. iCOVER was designed to be administered by peers, paraprofessionals, or medical personnel in 60-120 seconds, including in military operational environments. The term iCOVER is an acronym that s…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * ≥ 18 years and ≤ 50 years of age (if age not known, appears to be) * In the emergency department as a patient or loved one of a patient * If a patient, anticipated to be discharged to home from the emergency department after evaluation * Exhibiting visible signs of distress Ri…
Contacts

Jenni Shafer, PhD

919-360-0681

jenni_shafer@med.unc.edu

CONTACT

Allison Britt, BS

919-605-1046

allison_britt@med.unc.edu

CONTACT