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NCT Number: NCT03655769

fMRI Analysis of Aging and Awareness in Conditioning

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.

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Key information

Age range

20 year–30 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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).

Treatment and study plan

Transcranial Direct Current Stimulation

Device

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

Sham Transcranial Direct Current Stimulation

Device

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

Primary outcomes

  1. CS-US Awareness

    Time frame: recorded immediately after the 20 minutes of tDCS stimulation

    To 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 outcomes

  1. Line bisection test of left-hemifield neglect

    Time frame: recorded immediately after primary awareness questionnaire

    The 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.

  2. Eyeblink conditioned responding

    Time frame: recorded during the tDCS administration

    Eyeblink 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.

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Collaborators

  • National Institute on Aging (NIA)

Registry information

Official study title

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

Important dates

Study start
2010
Primary completion
2026
Study completion
2026
First posted
Aug 31, 2018
Registry last updated
Dec 11, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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