- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03994120
Modulating the Hippocampal and Striatal Memory Networks With rTMS
Background:
People have 2 memory systems. One helps them learn skills and the other helps them learn facts. Repetitive transcranial magnetic stimulation (rTMS) uses electric currents to activate brain cells. This can make small changes in how brain systems operate. Researchers will use rTMS to change how memory systems work and to see if changing one system causes the other to change too. This could help find ways to improve learning and memory in people with memory disorders.
Objective:
To learn how different memory systems work with each other.
Eligibility:
Healthy adults ages 18-40 who are not pregnant
Design:
Potential participants will be screened with a neurological exam if they have not had one from NINDS in the past 2 years. They may have urine tests.
Eligible participants will have 5-10 visits at NIH. Each visit will last 1-6 hours. Visits 1-4 will each take place 1 day apart.
At visit 1, participants will have an MRI and take memory tests. For MRI, they will lie on a table that slides in and out of a cylinder that takes pictures of their brain. They will also have rTMS. For rTMS, a metal coil is held on their scalp. Brief electrical currents pass through the coil.
At visits 2 and 3, participants will have rTMS.
At visit 4, participants will have an MRI and do memory tests.
About a week later, participants will have visit 5. They will have an MRI and do memory tests. Participants may be asked to have more visits if any technical problems occur. Participant involvement will last 2 weeks.
...
Study Overview
Detailed Description
Objective
The Behavioral Neurology Unit studies the human brain systems underlying learning and adaptation with the ultimate goal of finding interventions to make these processes more efficient. We are interested in whether repetitive transcranial magnetic stimulation (rTMS) can alter functional connectivity (FC) and behavioral efficiency in two memory networks in the brain: the hippocampal network, which supports the storage and retrieval of recallable facts, concepts, and events, and the striatal network, which supports the storage and retrieval of skills and habits. Additionally, because these networks interact behaviorally and can interfere with each other, an important question is whether neuromodulation of one network changes connectivity and efficiency in the other network. Pilot data from our group suggest that exogenous stimulation of one network causes it to expand its range of FC and co-opt resources from the other, which is a potential mechanism for the observed behavioral interaction. This study is designed to test a) whether rTMS- modulates within-network FC and memory supported by that network, and b) whether this also causes FC and behavioral changes in the other network.
Study population: Healthy Volunteers
Design
This study contains four between-subjects experiments and is a mixed inter/intra subject design. Experiment 1 will use nominally excitatory stimulation targeting the hippocampal network to increase FC within the hippocampal network. We also expect to increase FC between the hippocampal and striatal networks, increased declarative memory, and a possible decrease in procedural, learning. Experiment 2 will use excitatory stimulation targeted to the striatal network. We expect this to cause stronger within- network FC in the striatal network, increased FC between the hippocampus and the striatal network and concomitant behavioral effects. Experiments 3 and 4 will be similar except that we will target nominally inhibitory stimulation to these networks and look for the inverse results. FC will be measured under resting and task-activated conditions and active rTMS will be compared to vertex sham.
Outcome measures
The primary outcome measure is the change in FC produced by rTMS within the targeted network. Between-network FC changes and corresponding memory changes will be secondary outcomes. Exploratory measures will include correlations between individual cognitive differences (questionnaires and NIH Toolbox scores), and our primary and secondary outcome measures.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Maryland
-
Bethesda, Maryland, United States, 20892
- National Institutes of Health Clinical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
INCLUSION CRITERIA:
-Age 18-40 (inclusive)
EXCLUSION CRITERIA:
- Any current major neurological or psychiatric disorder such as (but not limited to) stroke, Parkinson disease, Alzheimer disease, schizophrenia or major depression
- History of seizure
- Medications acting on the central nervous system, such as those that lowers the seizure threshold such as neuroleptics, beta lactams, isoniazid, metronidazole; benzodiazepines, tricyclic or other antidepressants; or prescription stimulants.
- Ferromagnetic metal in the cranial cavity or eye, implanted neural stimulator, cochlear implant, or ocular foreign body
- Implanted cardiac pacemaker or auto-defibrillator or pump
- Non-removable body piercing
- Claustrophobia
- Inability to lie supine for 2 hours
- Pregnancy, or plans to become pregnant during the study.
- Members of the NINDS BNU
- Subjects that received rTMS under protocol 17-N-0055 are excluded in order avoid learning effects from previously being exposed to the same behavioral tasks
- Subjects who have contraindications to MRI (we will follow the NMR Center guidelines for MR safety). Some of the exclusions are:
Have non-MRI compatible metal in the body, such as a cardiac pacemaker, brain stimulator, shrapnel, surgical metal, clips in the brain or on blood vessels, cochlear implants, artificial heart valves or ferromagnetic fragments in the eye or oral cavity as these make having an MRI unsafe.
- Unable to lie flat on the back for the expected length of the experiment (2 hours).
- Have an abnormality on the brain imaging or neurologic examination not related to the diagnosis.
- Non-removable body piercing or
- Pregnancy (urine pregnancy test)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Motor Cortex rTMS
|
Altering the connectivity of trans-synaptic pathways
|
|
Active Comparator: PPC rTMS
|
Altering the connectivity of trans-synaptic pathways
|
|
Placebo Comparator: vertex rTMS
|
Altering the connectivity of trans-synaptic pathways
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change From Baseline in Resting-state Functional Connectivity Between the Caudate and the Caudate Network
Time Frame: Baseline, 1 day and 14-21 days after rTMS
|
Participants underwent repetitive transcranial magnetic stimulation (rTMS) to the caudate network, which supports learning skills.
rTMS uses electric currents to activate brain cells, which can temporarily change brain connections and memory.
We measured how rTMS affects caudate network brain connectivity.
These changes were observed with MRI.
To measure brain connection strength, we calculated how closely neural activity correlates in the caudate network.
We measured how rTMS affects connection strength before and 1 day after stimulation (immediate effects), and before and 14-21 days after stimulation (long-term effects) and then calculated the change as a Z-transformation score.
A change in the Fisher Z-transformation correlation coefficient score of 0 suggests no difference in the connections between brain areas after rTMS; a score of < 0 suggests a weakening of the connections between brain areas; and a score of > 0 suggests a strengthening of the connections between brain areas.
|
Baseline, 1 day and 14-21 days after rTMS
|
|
Change From Baseline in Task-based Functional Connectivity Between the Caudate and the Caudate Network
Time Frame: Baseline, one day and 14-21 days after rTMS
|
Participants underwent repetitive transcranial magnetic stimulation (rTMS) to the targeted memory network, i.e., caudate network.
rTMS uses electric currents to activate brain cells, which can temporarily change brain connections and memory.
We measured how rTMS affects caudate network brain connectivity on MRI during a Weather Prediction Task.
To measure brain connection strength, we calculated how closely neural activity correlates in the caudate network.
We measured how rTMS affects connection strength and skill learning by measuring them before and 1 day after stimulation (immediate effects), and before and 14-21 days after stimulation (long-term effects) and then calculated the change as a Z-transformation score.
A change in the Fisher Z-transformation score of 0 suggests no difference in the connections between brain areas; a score of < 0 suggests a weakening of the connections between brain areas; and a score of > 0 suggests a strengthening of connections between brain areas.
|
Baseline, one day and 14-21 days after rTMS
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feedback Weather Prediction Task (WPT-F)
Time Frame: Changes are calculated before and one day after rTMS and before and 14-21 days after rTMS
|
The Feedback Weather Prediction Task (WPT-F) tests the participant's ability to learn an association by trial and error.
One, two, or three-card combinations of four possible cards are presented on a computer and the subject is asked to predict the "weather;" i.e. whether it will be rainy or sunny.
After each prediction, the subject receives corrective feedback.
Each card is independently associated with one outcome with a fixed probability.
Participants learn the probabilistic relationship between stimuli and outcomes through feedback (reward).
The WPT-F was administered during the MRI session at three time periods, i.e., prior to rTMS, one day after rTMS, and 14-21 days after rTMS.
The proportion of trials where the participant selected the best option, i.e., the option most tightly linked to reward, was calculated at each visit.
Changes in scores between baseline and one day after and 14-21 days after rTMS were calculated.
|
Changes are calculated before and one day after rTMS and before and 14-21 days after rTMS
|
|
Observational Weather Prediction Task (WPT-O)
Time Frame: Changes are calculated before and one day after rTMS and before and 14-21 days after rTMS
|
The Observational Weather Prediction Task (WPT-O) is a paired associates test where the cue and feedback are displayed on the screen together.
After all pairs are shown the cards are again shown and the participant is asked to remember which feedback outcome (sun or rain) is paired with that set of cards.
Participants learn the pairing between sets of stimuli and one of two outcomes through memorization.
The WPT-O was administered during the MRI session at three time periods, i.e., prior to rTMS, one day after rTMS, and 14-21 days after rTMS.
The proportion of trials where the participant accurately remembered the pair, was calculated at each visit.
Changes in scores between baseline and one day after and 14-21 days after rTMS will be calculated.
|
Changes are calculated before and one day after rTMS and before and 14-21 days after rTMS
|
|
Change From Baseline in Resting-state Functional Connectivity Between the Caudate and the Hippocampal Network
Time Frame: Baseline, one day and 14-21 days after rTMS
|
Participants underwent repetitive transcranial magnetic stimulation (rTMS) to the hippocampal network, which supports learning skills.
rTMS uses electric currents to activate brain cells, which can temporarily change brain connections and memory.
We measured how rTMS affects hippocampal network brain connectivity.
These changes can be observed with MRI.
To measure brain connection strength, we calculated how closely neural activity correlates in the hippocampal network.
We measured how rTMS affects connection strength before and 1 day after stimulation (immediate effects), and before and 14-21 days after stimulation (long-term effects) and then calculated the change as a Z-transformation score.
A change in the Fisher Z-transformation score of 0 suggests no difference in the connections between brain areas after rTMS; a score of < 0 suggests a weakening of the connections between brain areas; and a score of > 0 suggests a strengthening of the connections between brain areas.
|
Baseline, one day and 14-21 days after rTMS
|
|
Change From Baseline in Task-based Functional Connectivity Between the Caudate and the Hippocampal Network
Time Frame: Baseline, one day and 14-21 days after rTMS
|
Participants underwent repetitive transcranial magnetic stimulation (rTMS) to the targeted memory network, i.e., hippocampal network.
rTMS uses electric currents to activate brain cells, and this can temporarily change brain connections and memory.
We measured how rTMS affects hippocampal network brain connectivity on MRI during a Weather Prediction Task.
To measure brain connection strength, we calculated how closely neural activity correlates in the hippocampal network.
We measured how rTMS affects connection strength and skill learning before and 1 day after stimulation (immediate effects), and before and 14-21 days after stimulation (long-term effects) and then calculated the change as a Z-transformation score.
A change in the Fisher Z-transformation score of 0 suggests no difference in the connections between brain areas; a score of < 0 suggests a weakening of the connections between brain areas; and a score of > 0 suggests a strengthening of the connections between brain areas.
|
Baseline, one day and 14-21 days after rTMS
|
Collaborators and Investigators
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 190114
- 19-N-0114
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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