Recruiting

Observational Study

Sponsor:

Georgia Institute of Technology

Code:

NCT03896529

Conditions

Aging

Anxiety

Memory Impairment

Eligibility Criteria

Sex: All

Age: 65 - 70+

Healthy Volunteers: Accepted

Interventions

Anticipatory psychological stress

Study Details

Brief summary:

Two hallmarks of both healthy aging and age-related disease are 1) memory and navigational deficits, particularly in orienting towards goal locations and planning how to navigate to them, and 2) increased susceptibility to stress and altered regulation of the stress response. However, there are marked individual differences in these age-related changes. The investigators' proposal will help characterize factors that contribute to this variability.

Participants will be pseudorandomly assigned to stress-manipulated or control groups. The investigators will give both groups a novel immersive navigation task, validated by the PI in healthy young adults. This paradigm gives participants the opportunity to either (a) flexibly draw on spatial memory in order to plan efficient routes to goal locations, or (b) fall back on inefficient, but cognitively less-demanding, stimulus-response associations (i.e., habits). Using neuroimaging and behavioral measures, the investigators' protocol will test whether experimentally-induced stress leads individuals to bring fewer details about future locations to mind when route planning, and whether such restricted prospective thought ultimately biases participants towards relatively inflexible, habitual actions.

Conditions

Aging

Anxiety

Memory Impairment

Study ID

NCT03896529

Start date

Sep 24, 2019

Status verified date

Nov, 2025

Completion date

Sep 1, 2026

Anticipated

Primary completion date

Sep 1, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 65 - 70+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • adults 65-80
  • U.S. citizens or permanent residents
  • who speak fluent English
  • willing to come to Georgia Tech to participate in group testing sessions.

Exclusion Criteria:

  • Individuals will be carefully screened using IRB-approved procedures for safety contraindications to MRI and electrical shock stimulation
  • (e.g., metal or electrical implants, heart arrhythmia, or medication affecting the cardiovascular system \[e.g. beta-blockers\]).

The purpose of this study is to investigate mechanisms of normally functioning memory, and memory-related changes in healthy aging. Thus, any confounding factors that may influence cognition, other than age, will be exclusionary. Potential participants that endorse any of the following conditions will be excluded from the study:

  • Epilepsy
  • Dementia
  • Parkinson's disease
  • history of stroke or seizure
  • psychiatric disorders
  • untreated depression or emotional conditions
  • Attention Deficit Disorder
  • Multiple Sclerosis
  • uncontrolled hyper- or hypo-tension
  • untreated Diabetes
  • Sickle Cell Anemia
  • regularly use illegal or psychoactive drugs (e.g., cocaine, alcohol abuse, etc).
  • Additionally, individuals scoring < 3 on WAIS-R forward span, < 2 on WAIS-R backward span, and failing to name more than 2 vegetable names will be excluded from the study. These exclusions will insure that persons with mild cognitive impairment or typical indications of clinical dementia will be not participate in the research.

Study Design

Enrollment

85 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Basic Science

Interventions and Outcome Measures

Arms

no intervention: No-stress control group

Participants in this group will perform the psychology tasks (virtual navigation) without any manipulation of psychological stress

experimental: Stress group

Participants in this group will perform the psychology tasks (virtual navigation) under manipulated psychological stress (anticipatory threat of shock)

Interventions

Anticipatory psychological stress

Unpredictable delivery of low-level electrical stimulation to left ankle periodically throughout psychology tasks (virtual navigation). Established procedure for inducing anticipatory stress.

Primary outcome measure

  • Behavioral probability of taking a shortcut between control and treatment groups [ Time Frame: Approximately 1.5 years ]
  • fMRI activation level between control and treatment groups [ Time Frame: Approximately 1.5 years ]
  • Neural memory representation reactivation between control and treatment groups [ Time Frame: Approximately 1.5 years ]

Central Contacts and Locations

Central contacts

Locations

Center for Advance Brain Imaging

Recruiting

Atlanta, Georgia, United States, 30318

Contacts

Vishwadeep Ahluwalia, Ph.D.

404-385-8619vahluwalia7@gatech.edu

Principal Investigator:

Brown Thackery, Ph.D

More Information

Sponsor

Georgia Institute of Technology

Last update posted

Apr 17, 2026

Last verified

Nov, 2025

Keywords

  • Aging
  • Spatial Memory
  • Stress
  • fMRI

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Georgia Institute of Technology on 2026-04-17.