NCT05558527

Brief 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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
45

participants targeted

Target at P25-P50 for not_applicable

Timeline
43mo left

Started Dec 2025

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress10%
Dec 2025Dec 2029

First Submitted

Initial submission to the registry

August 12, 2022

Completed
2 months until next milestone

First Posted

Study publicly available on registry

September 28, 2022

Completed
3.2 years until next milestone

Study Start

First participant enrolled

December 18, 2025

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2028

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2029

Last Updated

April 13, 2026

Status Verified

February 1, 2026

Enrollment Period

3 years

First QC Date

August 12, 2022

Last Update Submit

April 6, 2026

Conditions

Keywords

psychological traumaethnoracial discriminationhypervigilanceanticipated threatsocial emotion regulationsocial touch

Outcome Measures

Primary Outcomes (3)

  • 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

  • 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

  • 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

Study Arms (3)

Social support from a romantic partner

EXPERIMENTAL

Participants will hold the hand of their romantic partner

Behavioral: social support

Social support from a stranger

ACTIVE COMPARATOR

Participants will hold the hand of a stranger

Behavioral: social support

No social support

NO INTERVENTION

Participants will hold a stress ball

Interventions

social supportBEHAVIORAL

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

Social support from a romantic partnerSocial support from a stranger

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • In a stable romantic relationship for 6 months or more
  • Normal vision or corrected-to-normal vision
  • Fluent in English

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Nevada, Reno

Reno, Nevada, 89557, United States

RECRUITING

MeSH Terms

Conditions

Historical TraumaRacismEmotional RegulationAnxiety DisordersPsychological Trauma

Condition Hierarchy (Ancestors)

Stress Disorders, TraumaticTrauma and Stressor Related DisordersMental DisordersPrejudiceSocial BehaviorBehaviorSocial DiscriminationSelf-Control

Study Officials

  • Cynthia L Lancaster, PhD

    University of Nevada, Reno

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Kylie Baer, MS

CONTACT

Cynthia L Lancaster, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor Psychology/Associate Director, Clinical Training

Study Record Dates

First Submitted

August 12, 2022

First Posted

September 28, 2022

Study Start

December 18, 2025

Primary Completion (Estimated)

December 1, 2028

Study Completion (Estimated)

December 1, 2029

Last Updated

April 13, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will share

de-identified data including primary and secondary outcomes

Shared Documents
STUDY PROTOCOL, SAP, ICF
Time Frame
within 6 months after publication
Access Criteria
email request to the study PI (cynthialancaster@unr.edu)

Locations