NCT07055555

Brief Summary

The goal of this study is to better understand how stress impacts people's ability to learn across their experiences and link new information to what they already know. The investigators will compare performance on a memory task between stressed and non-stressed participants. This memory task requires people to integrate knowledge across learning experiences (think: having to "connect the dots", draw inferences, and generalize your knowledge to new situations and scenarios). Cortisol, the brain's primary stress hormone, will be measured at multiple points throughout the study to measure stress levels. The investigators hypothesize that:

  1. 1.Stress will disrupt performance on the memory task by interfering with memory processes that enable linking of related memories.
  2. 2.Higher cortisol levels, which reflect a greater stress response, will relate to greater deficits in memory performance across participants.

Trial Health

75
On Track

Trial Health Score

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

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
15mo left

Started Jul 2025

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
active not 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 Progress41%
Jul 2025Jul 2027

First Submitted

Initial submission to the registry

June 5, 2025

Completed
26 days until next milestone

Study Start

First participant enrolled

July 1, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 9, 2025

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2026

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2027

Last Updated

August 15, 2025

Status Verified

August 1, 2025

Enrollment Period

1.1 years

First QC Date

June 5, 2025

Last Update Submit

August 12, 2025

Conditions

Keywords

acute stressmemorymemory integrationcognitive maps

Outcome Measures

Primary Outcomes (1)

  • Performance on A-C inference trials in the Paired Associative Inference Task

    Performance on A-C inference trials of the memory task assesses memory integration across overlapping learning experiences.

    During the participant's study visit, anticipated 1-2 hours

Secondary Outcomes (1)

  • Performance on directly learned pairs (A-B and B-C) in the Paired Associative Inference Task

    During the participant's study visit, anticipated 1-2 hours

Study Arms (2)

Acute Stress Condition

EXPERIMENTAL

Participants randomized to the acute stress condition will complete the Trier Social Stress Test (TSST), a validated experimental method for inducing acute psychosocial stress. This condition will allow for us to evaluate our primary hypothesis.

Behavioral: Acute Stress

Non-Stress Control Condition

SHAM COMPARATOR

Participants randomized to the non-stress control condition will complete a non-stressful task designed to parallel the structure of the Trier Social Stress Test without eliciting acute stress.

Behavioral: Non-Stress Control Task

Interventions

Acute StressBEHAVIORAL

Participants randomized to the acute stress condition will complete the Trier Social Stress Test (TSST), a validated experimental method for inducing acute psychosocial stress. The TSST consists of a brief anticipation period followed by a 5-minute mock job interview and a 5-minute surprise mental arithmetic task, performed in front of a neutral panel of judges in professional attire.

Also known as: Trier Social Stress Test
Acute Stress Condition

Participants randomized to the control condition will complete a non-stressful task designed to parallel the structure of the Trier Social Stress Test without eliciting acute stress. They will have a brief anticipation period followed by a 5-minute description of their typical day or favorite hobby. This task is conducted without an evaluative panel, minimizing the potential for stress or anxiety.

Non-Stress Control Condition

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • healthy adults
  • aged 18-35 years
  • speak fluent English
  • have normal or corrected-to-normal vision

You may not qualify if:

  • individuals who are pregnant
  • exercise within 1 hour of the study session
  • smoking within 1 hour of the study session
  • consuming drugs or alcohol within 1 hour of the study session

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nevada State University

Henderson, Nevada, 89002-9776, United States

Location

MeSH Terms

Interventions

Psychological Tests

Intervention Hierarchy (Ancestors)

Behavioral Disciplines and Activities

Study Officials

  • Corey A Fernandez, PhD, Neuroscience

    Nevada State University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 5, 2025

First Posted

July 9, 2025

Study Start

July 1, 2025

Primary Completion (Estimated)

July 31, 2026

Study Completion (Estimated)

July 31, 2027

Last Updated

August 15, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will share

De-identified data, including demographic and outcome measures, will be made available to qualified researchers upon request after publication of findings. Data will be shared under a data use agreement via a secure repository such as Open Science Framework (OSF).

Locations