NCT07460453

Brief Summary

Paranoia is a pattern of thinking in which people feel suspicious or believe others may want to harm them. It can occur in many people, not only those with a mental health diagnosis, and it can affect daily life, relationships, and overall well-being. Research has consistently shown that Black Americans report higher levels of paranoia than White Americans, even when they do not have a clinical diagnosis. However, the reasons for this difference are not well understood. The goal of this study is to better understand why these differences exist. In the experimental part of the study, researchers will use a randomized design to test whether exposure to stressful experiences related to race leads to higher levels of paranoia among Black American participants. The study will also examine factors that may strengthen or weaken this effect, such as individual experiences and personal characteristics. By identifying how stressful experiences related to race influence paranoia, this research aims to improve how paranoia is measured and understood across different groups. These findings may help researchers and clinicians use more accurate and culturally appropriate tools to assess psychosis-related experiences in diverse populations.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
480

participants targeted

Target at P75+ for not_applicable

Timeline
2mo left

Started Apr 2026

Shorter than P25 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 Progress32%
Apr 2026Jun 2026

First Submitted

Initial submission to the registry

March 4, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 10, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

April 13, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2026

Last Updated

April 29, 2026

Status Verified

April 1, 2026

Enrollment Period

3 months

First QC Date

March 4, 2026

Last Update Submit

April 28, 2026

Conditions

Keywords

ParanoiaPsychosis-SpectrumAdverse ExperiencesExperimental ParadigmGeneral Population

Outcome Measures

Primary Outcomes (1)

  • State Paranoia

    Self-reported paranoia will be assessed immediately following the experimental task to capture acute, experimentally induced changes in paranoia. State paranoia will be measured using the Revised Green Paranoid Thought Scale (R-GPTS; Green et al., 2019), an 18-item validated Likert-type measure appropriate for clinical and nonclinical samples. Scores range from 0-72, with higher scores indicating greater state paranoia. The R-GPTS includes two subscales: (1) Ideas of Reference and (2) Ideas of Persecution. Items are summed to generate subscale and total scores. The scale demonstrates excellent internal consistency (α \> .90), and prior work (Wolny et al., revisions submitted) established measurement invariance across Black and White American participants.

    Immediately post-intervention (single session)

Secondary Outcomes (1)

  • Affective Response

    Pre-intervention and immediately post-intervention

Other Outcomes (2)

  • Imagery Vividness and Task Engagement

    Immediately post-intervention

  • Perceived Stress During Task

    Immediately post-intervention

Study Arms (4)

Blatant Race-Related Adverse Experience Imagery

EXPERIMENTAL

Participants are exposed to an audio-guided imagery scenario depicting a blatant race-related adverse experience. The guided imagery task instructs participants to vividly imagine a situation involving explicit racial hostility or discrimination. This intervention is designed to experimentally prime exposure to overt race-related social threat in a controlled setting.

Behavioral: Guided Visual Imagery Task

Subtle Race-Related Adverse Experience Imagery

EXPERIMENTAL

Participants are exposed to an audio-guided imagery scenario depicting a subtle race-related adverse experience, such as ambiguous or indirect racial bias. The guided imagery task instructs participants to imagine a situation involving covert or nuanced race-related social threat, consistent with commonly reported microaggressive experiences.

Behavioral: Guided Visual Imagery Task

Neutral Control Imagery

PLACEBO COMPARATOR

Participants are exposed to an audio-guided imagery scenario depicting a neutral, non-threatening experience unrelated to race or social evaluation. This condition serves as a control for engagement with the guided imagery task without exposure to race-related adverse content.

Behavioral: Guided Visual Imagery Task

Social Exclusion Imagery

EXPERIMENTAL

Participants listen to an audio-guided imagery scenario depicting social exclusion (e.g., being left out or rejected in a social context) without reference to race and are instructed to vividly imagine the situation. This condition isolates the effect of social threat/exclusion from race-specific content.

Behavioral: Guided Visual Imagery Task

Interventions

Participants complete an online, audio-guided visual imagery task designed to experimentally prime social experiences under standardized conditions. After brief instructions to imagine themselves actively participating in each scene, participants complete practice trials with neutral content and then are randomized to listen to one audio-recorded scenario matched to their assigned condition. Each trial includes a brief relaxation period, an instruction period, a guided imagery listening period, and a short recovery period. Scenarios are approximately 30 seconds and are delivered via headphones/speakers within the survey platform. Following the imagery task, participants complete post-task self-report assessments capturing current (state) experiences, including state paranoia and manipulation checks (e.g., imagery vividness and task engagement). The task is administered once in a single session.

Blatant Race-Related Adverse Experience ImageryNeutral Control ImagerySocial Exclusion ImagerySubtle Race-Related Adverse Experience Imagery

Eligibility Criteria

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

You may qualify if:

  • years of age or older
  • Self-identify as non-Hispanic Black or African American
  • Currently reside in the United States
  • Speak and read English
  • Registered as a survey participant on the Prolific platform

You may not qualify if:

  • Younger than 18 years of age
  • Do not self-identify as non-Hispanic Black or African American
  • Do not currently reside in the United States
  • Do not speak or read English
  • Not registered as a survey participant on the Prolific platform

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Psychological and Brain Sciences

Bloomington, Indiana, 47405, United States

RECRUITING

MeSH Terms

Conditions

Paranoid DisordersPsychotic Disorders

Condition Hierarchy (Ancestors)

Schizophrenia Spectrum and Other Psychotic DisordersMental Disorders

Central Study Contacts

William Hetrick

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Provost Professor Psychological and Brain Sciences

Study Record Dates

First Submitted

March 4, 2026

First Posted

March 10, 2026

Study Start

April 13, 2026

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

June 30, 2026

Last Updated

April 29, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be publicly shared. Due to the sensitive nature of the data collected, individual-level data are not planned for open distribution. De-identified aggregate results will be reported in publications. Potential data collaborations may be considered on a case-by-case basis, subject to institutional and ethical review.

Locations