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fMRI Analysis of Aging and Awareness in Conditioning

Functional Magnetic Resonance Imaging (fMRI) Analysis of Aging and Awareness in Conditioning

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03655769
Enrollment
16
Registered
2018-08-31
Start date
2010-11-09
Completion date
2026-12-31
Last updated
2025-12-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Transcranial Direct Current Stimulation

Brief summary

Cathodal Transcranial direct current stimulation (tDCS) was administered to the right parietal region in order to determine if this stimulation could disrupt awareness of the conditioned stimulus (CS) - unconditioned stimulus (US) relationship in a classical conditioning experiment.

Interventions

DEVICEtranscranial direct current stimulation

transcranial direct current stimulation applied at 2 mA over the right parietal region for 20 min

DEVICEsham transcranial direct current stimulation

transcranial direct current stimulation applied at 2 mA over the right parietal region for 30 sec

Sponsors

National Institute on Aging (NIA)
CollaboratorNIH
Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Educational attainment of at least eight years and English as the native language * Mini-Mental State Examination (MMSE) score of 26 * Normal episodic memory (i.e., CERAD word List Recall \> 5) * Informed consent; 5) age of 20-30

Exclusion criteria

* Disturbed consciousness * Other neurological or systemic disorder which can cause dementia or cognitive dysfunction * Prior history of a major psychiatric disorder * History of definite stroke * Focal lesion on MRI exam * Use of anxiolytic, antidepressant, neuroleptic, or sedative medication * Predominately left-handed * Has MRI contraindication such as pacemaker, implanted pumps, shrapnel, etc. (full MRI screening form will be filled out).

Design outcomes

Primary

MeasureTime frameDescription
CS-US Awarenessrecorded immediately after the 20 minutes of tDCS stimulationTo assess CS-US awareness, we used a questionnaire The questionnaire consists of 7 true/false questions about the sequence and co-occurrence of the conditioned stimulus (CS, a 1000 Hz tone) and unconditioned stimulus (US, a 100 ms puff of air to the eye). The score can thus range from 0 to 7. Higher score values indicate better awareness of the sequence and co-occurrence of the CS and US

Secondary

MeasureTime frameDescription
Line bisection test of left-hemifield neglectrecorded immediately after primary awareness questionnaireThe subject is given a sheet of paper with a number of horizontal lines on it. The subject is instructed to cut each line in half by drawing a small pencil mark through each line. The test is scored by measuring the percent deviation, which is calculated by the following formula: Percent deviation=100 x (measured left half - true half)/true half This yields positive numbers for marks placed to the right of center, and negative numbers for marks placed to the left of center. Patients with right hemisphere damage and contralateral neglect show higher positive line bisection scores compared to healthy controls or patients without right hemisphere damage and vice versa.
Eyeblink conditioned respondingrecorded during the tDCS administrationEyeblink conditioning is recorded while the subject watches a silent movie. For conditioning, the conditioned stimulus (CS) is a 1350 ms 1000 Hz tone. This tone co-terminates with a 100 ms left corneal airpuff (5 psi). 30 CS-US presentations are delivered at an average rate of one every 18 sec. Conditioned responses (CRs) are defined as follows: the difference between the maximum and minimum responses in a 500 ms pre-US time window must exceed four times the standard deviation of the mean of the baseline period (250 ms pre-CS presentation). The 500 ms pre-US time window was selected to minimize the inclusion of voluntary and alpha responses as CRs. Performance is expressed as % CRs, that is, the percent of trials in which a CR occurred. Greater numbers indicate greater amounts of learning.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026