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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05558527
Other study ID # 1883993-2
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 2024
Est. completion date December 2026

Study information

Verified date April 2024
Source University of Nevada, Reno
Contact Anna C Cole, MA
Phone (775) 682-8145
Email accole@nevada.unr.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will examine the effects of social support on threat vigilance and arousal using eye tracking. We will also test the moderating effects of trauma and discrimination history.


Description:

Both interpersonal trauma (IPT) and ethno-racial discrimination amplify risk for hyper-arousal symptoms of posttraumatic stress disorder (PTSD), but the mechanism of this effect is unclear. Prior research suggests that social support plays an important role in regulating emotional responses, a process called social emotion regulation. This study will test whether a history of IPT and/or ethno-racial discrimination influence the social regulation of arousal and vigilance. Social regulation will be tested by contrasting responses under conditions with and without social support.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 45
Est. completion date December 2026
Est. primary completion date December 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - In a stable romantic relationship for 6 months or more - Normal vision or corrected-to-normal vision - Fluent in English Exclusion Criteria: - If vision is corrected-to-normal, needs to use hard contact lenses, bifocal contact lenses, or glasses - Experienced a traumatic event within the past 4 weeks

Study Design


Intervention

Behavioral:
social support
social support is provided in the form of social touch (hand holding)

Locations

Country Name City State
United States University of Nevada, Reno Reno Nevada

Sponsors (1)

Lead Sponsor Collaborator
University of Nevada, Reno

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Vigilance Related Eye Movements - Number of Eye Fixations Participants will view 15 pictures of natural environmental scenes for 10 seconds per image. We will use an eye tracker to examine the number of eye fixations per scene. A greater number of fixations during the 10 second presentation of a scene would indicate greater vigilance. Collected from minute 15 to minute 45 of study participation, approximately
Primary Vigilance Related Eye Movements - Visual Scanning Participants will view 15 pictures of natural environmental scenes for 10 seconds per image. We will use an eye tracker to examine the proportion of the scene that they look at (fixate on) out of approximately 80 possible sectors. A greater proportion of the scene they fixate on would indicate greater vigilance. Collected from minute 15 to minute 45 of study participation, approximately
Primary Threat-Related Physiological Arousal - Pupil Dilation Participants will view a series of visual cues (either an 'X' or an 'O') where an 'X' signals a possible (20% probability) aversive auditory stimulus (human scream). We will examine pupil dilation during the task in order to measure arousal in response to uncertain threat. We will calculate average pupil dilation during the wait period after threat cues (X) and after safety cues (O). We will subtract average pupil dilation after safety cues from threat cues to create an index of threat-related arousal. Greater pupil dilation (for threat minus safety cues) would indicate greater threat-related arousal. Collected from minute 45 to minute 75 of study participation, approximately
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