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Study identifier: NCT06482567 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Promoting Improved Functioning Among People Experiencing Stressful Situations

Condition: Acute Stress Reaction  ·  Sponsor: University of North Carolina, Chapel Hill

PhaseNA
Planned participants450
Who can joinAll sexes, 18 Years to 50 Years
Healthy volunteersNo

About this study

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 summarizes the six specific steps of the intervention: (1) identify that an individual is experiencing an ASR; (2) Connect with the individual through word, eye contact, and physical touch to draw them back to the present moment; (3) Offer commitment so that the individual feels less psychologically isolated and withdrawn (e.g., "I'm right here with you"); (4) Verify facts - ask simple fact-based questions to engage the individual in deliberate cognitive activity; (5) Establish order of events - briefly review what has happened, what is happening, and what will happen to orient the individual; and (6) Request action to re-engage the individual in purposeful behavior. Participants will be randomly assigned to one of three groups: iCOVER, usual care, or physical presence with reassurance. Investigators have elected to use two different control conditions, in order to examine the reliability of the iCOVER intervention in comparison with two typical responses to individuals experiencing an ASR (i.e., physical presence with reassurance, no specific treatment).

This description comes directly from the study's public registry record.

Talk to the study team

Jenni Shafer, PhD  ·  919-360-0681  ·  jenni_shafer@med.unc.edu

Allison Britt, BS  ·  919-605-1046  ·  allison_britt@med.unc.edu

Always discuss trial participation with your own doctor first.

Locations (5)

McLean Hospital, Harvard Medical SchoolBelmont, Massachusetts, United StatesActive Not Recruiting
University of Massachusetts Chan Medical SchoolWorcester, Massachusetts, United StatesRecruiting
Henry Ford Health SystemDetroit, Michigan, United StatesRecruiting
Washington University, St. LouisSt Louis, Missouri, United StatesRecruiting
Cooper University Health CareCamden, New Jersey, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06482567