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Modulation of the Parieto-frontal Communication

Modulation of the Parieto-frontal Communication

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03434093
Enrollment
0
Registered
2018-02-15
Start date
2019-02-03
Completion date
2019-02-25
Last updated
2019-02-28

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

Conditions

Normal Physiology

Keywords

Paired Associative Stimulation (PAS), Functional Magnetic Resonance Imaging (fMRI), Electrical Field Modeling, Working Memory

Brief summary

Background: Research shows that the parietal and prefrontal areas of the brain are involved in short-term memory. Researchers want to look at the effects of transcranial magnetic stimulation (TMS) of these areas on short-term memory and brain activity. They will use functional magnetic resonance imaging (fMRI) to look at brain activity. Objective: To look at the effects of TMS on brain pathways involved in memory. Eligibility: Healthy, right-handed adults ages 18-50 Design: Participants will have 3 or 4 visits at least 1 week apart. They cannot drink alcohol for at least 48 hours before each visit. The screening visit lasts about 1 (Omega) hours. It can be combined with the first testing visit. Screening includes: * Medical history * Physical exam * Neurological exam * Urine tests * Questionnaires about being left or right handed and about their ability to imagine physical activities. The first testing visit lasts about 1 (Omega) hours and includes an MRI. For the MRI, participants lie on a table that slides into a machine. They will lie still or perform simple memory tasks on a computer screen. The second and third testing visits last about 3 hours. Participants will have: * 2 MRIs * TMS: A wire coil is held to the scalp. A brief electrical current passes through the coil to create a magnetic pulse that affects brain activity. They will perform simple memory tasks. * EMG: Small electrodes are taped to the skin to record muscle activity while they rest. After the study, participants will complete a questionnaire about any discomfort they experienced during the study. ...

Detailed description

Objective: This study aims to identify whether repetitive dual-site transcranial magnetic stimulation (TMS) can modulate the functional connectivity between the parietal and dorso-lateral prefrontal cortices. Study population: The study involves 26 healthy volunteers. Design: This controlled study comprises 3 main visits for each subject: (1) a baseline, evaluation visit during which fMRI will be acquired during a visual short memory task along with diffusion tensor imaging and structural MRI; (2) a visit during which resting state fMRI (rsfMRI) will be acquired, followed by paired-associative stimulation (PAS) with pulses delivered over the parietal and then over the dorso-lateral prefrontal cortex, in order to induce a temporary plastic change in the interaction between the parietal and prefrontal cortices; the PAS will be followed by another rsfMRI and task fMRI; (3) a visit identical to #2 during which the PAS will be delivered with pulses in reverse order of previous visit. Outcome measures: The effects of PAS will be quantified with rsfMRI and a short working memory task, considered as a proxy for complex motor and cognitive control. * The primary outcome will be to investigate the resting state functional connectivity changes induced by each PAS intervention * The secondary outcome #1 will be to evaluate the difference in visual angle error between sessions 2 and 3 in a working memory task during which the subjects will be asked to remember the position of a bar presented on the screen at different time intervals before the inquiry. * The secondary outcome #2 will be to build an fMRI-DTI analysis pipeline for generation of TMS targets individually customized for each subject and a given task.

Interventions

DEVICETranscranial Magnetic Stimulation (TMS)

Description: This will comprise single and repeated paired-pulses delivered over motor and non-motor areas.

This will consist in remembering an item presented 1 to 5 steps before the inquiry. This task will span the whole duration of the functional MRI acquisition.

Sponsors

National Institute of Neurological Disorders and Stroke (NINDS)
Lead SponsorNIH

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* INCLUSION CRITERIA: * Age between 18-50 years. * Right-handed (handedness questionnaire will be part of the initial evaluation) * Able to give informed consent. * Have a normal neurological exam within the last year and MoCA\>27 * Willing and able to abstain from alcohol for at least 48 hours prior to the study. * Willing to not participate in other rTMS studies in the week preceding visits for the current protocol.

Exclusion criteria

-All participants must be able to undergo MRI and TMS, for which the MRI- and TMS-safety checklists will be part of the initial evaluation, and reconfirmed at the beginning of every visit. It will constitute as

Design outcomes

Primary

MeasureTime frame
Resting state functional connectivity change induced by the paired associative stimulationStudy completion

Secondary

MeasureTime frame
Difference in the visual angle error of a working memory task between the DLPFC-PCC and PPC-DLPFC paired associative stimulationStudy completion

Outcome results

None listed

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