CClinicalTrials.gg
TerminatedNCT04961645Updated Apr 24, 2025Results posted

Brain Stimulation and Visually-guided Navigation

An interventional study of Repetitive Transcranial Magnetic Stimulation (rTMS) and Computer-based Test in Healthy Participants, sponsored by Emory University. Terminated at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-04-24.

Sponsored by Emory University · Not applicable, Interventional, and Basic science

Why this study was terminated
The study was terminated in February 2025 after interim analyses among participants in the computer-based task study arm showed that the rTMS was not a successful method of evaluating involvement of OPA in visually-guided navigation.
Phase
Not applicable
Study type
Interventional
Enrollment
11
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

This study investigates the neural mechanisms causally involved in how people navigate through their immediately visible environment (e.g., walking around one's bedroom flawlessly and effortlessly, not bumping into the walls or furniture). To investigate whether particular neural mechanisms are causally involved in "visually-guided navigation", repetitive transcranial magnetic stimulation (rTMS) is used to temporarily disrupt the functioning of particular brain regions in healthy adults while they are shown simple visual stimuli of places (e.g., bedrooms, kitchens, and living rooms) and asked to perform simple computer tasks or to complete simple behavioral tasks.

Read the detailed description

Human ability to navigate through the immediately visible environment is crucial for survival. However, the representations and computations underlying this remarkable ability are not well understood, and current computer vision algorithms (robots) still lag far behind human performance. One promising strategy for attempting to understand "visually-guided navigation" is to characterize the neural systems that accomplish it. The results from functional magnetic resonance (fMRI) on adult humans have begun to elucidate the cortical regions involved in visually-guided navigation, with the central finding that there is at least one visual cortical region - called the occipital place area (OPA) that may play a central role in the ability to navigate through currently visible places (e.g., walking around our bedroom flawlessly and effortlessly, not bumping into the walls or furniture our bedroom). However, fMRI is a correlational method, and research still needs to determine if this functionally specific brain region is causally involved in visually-guided navigation. Understanding the causal involvement of this region will provide important clues about how humans navigate their world, and also perhaps someday be harnessed to help those individuals who devastatingly lose the ability to navigate, as a result of eye diseases, brain surgery, stroke, neurodegenerative diseases, or developmental disorders.

The use of rTMS to investigate the causal involvement of particular brain regions in particular human abilities is not novel, having been used to investigate face recognition, scene recognition, and object recognition. The general question for this research is to determine, using rTMS, the causal involvement of OPA in visually-guided navigation.

Participants will have an fMRI scan to identify the OPA location in each individual participant. Once the OPA location is known, participants will receive the rTMS study intervention.

02

Conditions studied

  • Healthy Participants

Keywords

  • Visually-guided navigation
03

In context

Lead sponsor

Emory University is the lead sponsor of 1,386 studies on the registry; 236 are open to participants now.

Of its 229 completed or terminated interventional studies of FDA-regulated products, 174 (76%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Normal or corrected-to-normal vision

Exclusion criteria

Exclusion Criteria:

  • Metal in the body
  • Personal or first-degree family history of epileptic seizure
  • A known brain injury
  • Claustrophobia
  • Taking certain medications that may increase the risk of seizures (e.g., bupropion, varenicline, chlorpromazine, theophylline) or reduce the effects of rTMS, such as benzodiazepines
  • Adults who are unable to consent, pregnant women, and prisoners
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
11 participants (actual)

Study arms

  • Experimental
    Repetitive Transcranial Magnetic Stimulation (rTMS) During Computer-based Task

    Participants receiving rTMS while they perform computer-based tests to examine the causal involvement of OPA in visually-guided navigation. The study visit lasts approximately 90 minutes.

    Device: Repetitive Transcranial Magnetic Stimulation (rTMS) · Behavioral: Computer-based Test

  • Experimental
    Repetitive Transcranial Magnetic Stimulation (rTMS) During Behavioral-based Task

    Participants receiving rTMS while they perform behavioral-based tests to examine the causal involvement of OPA in visually-guided navigation. The study visit lasts approximately 90 minutes.

    Device: Repetitive Transcranial Magnetic Stimulation (rTMS) · Behavioral: Behavioral-based Test

Interventions

  • DeviceRepetitive Transcranial Magnetic Stimulation (rTMS)

    TMS is a safe and noninvasive method for affecting brain function relying on the properties of electromagnetic induction. Action potentials are triggered in neurons, along with a subsequent period of deactivation. Normal ongoing brain activity is disrupted providing a way for investigators to produce a transient and reversible period of brain disruption.

  • BehavioralComputer-based Test

    Participants will be seated comfortably in a chair and asked to complete a simple computer-based task where they imagine walking through a room and press a button indicating if they can leave through a door on the left, center, or right wall. During or just before each of these tasks, participants will receive rTMS. In rTMS, a small plastic coil is placed next to the participant's head. The coil will be placed over the relevant brain region identified during the participant's fMRI scan. The coil will then generate a magnetic pulse, and stimulation will occur.

  • BehavioralBehavioral-based Test

    Participants will be asked to complete a simple behavioral task that will require them to walk around in a small room and search for hidden objects. During or just before each of these tasks, participants will receive rTMS. In rTMS, a small plastic coil is placed next to the participant's head. The coil will be placed over the relevant brain region identified during the participant's fMRI scan. The coil will then generate a magnetic pulse, and stimulation will occur.

06

What researchers measure

Primary outcomes

  1. Accuracy During Visually-guided Navigation Computer-based Task

    To assess performance during the visually-guided navigation computer-based task, rTMS is applied to to the control vertex site, which is not implicated in visually-guided navigation, as well as the occipital place area (OPA) site. While participants are shown simple visual stimuli of places (e.g., bedrooms, kitchens, and living rooms) they are asked to perform simple computer-based tasks (e.g., imagine they are walking through the room, and respond via button press whether they can leave through a door on the left, center, or right wall, as indicated by a continuous path on the floor). Performance is measured in task accuracy (the percentage of tasks performed correctly). A decrease in performance on the visually-guided navigation task only after rTMS is applied to OPA (but not vertex) indicates causal involvement of OPA in visually-guided navigation.

    Time frame: During rTMS of control site and during rTMS of OPA, on Day 1

  2. Reaction Time During Visually-guided Navigation Computer-based Task

    To assess performance during the visually-guided navigation computer-based task, rTMS is applied to to the control vertex site, which is not implicated in visually-guided navigation, as well as the occipital place area (OPA) site. While participants are shown simple visual stimuli of places (e.g., bedrooms, kitchens, and living rooms) they are asked to perform simple computer-based tasks (e.g., imagine they are walking through the room, and respond via button press whether they can leave through a door on the left, center, or right wall, as indicated by a continuous path on the floor). Performance is measured in the time (in milliseconds) that it takes to complete the task correctly. A decrease in performance on the visually-guided navigation task only after rTMS is applied to OPA (but not vertex) indicates causal involvement of OPA in visually-guided navigation.

    Time frame: During rTMS of control site and during rTMS of OPA, on Day 1

  3. Accuracy During Visually-guided Navigation Behavioral-based Task

    To assess performance during the visually-guided navigation behavior-based task, rTMS is applied to to the control vertex site, which is not implicated in visually-guided navigation, as well as the occipital place area (OPA) site. Participants are asked to complete simple behavioral-based tasks (e.g., actually walk around a small room and search for hidden objects). Performance is measured in task accuracy (the percentage of tasks performed correctly). A decrease in performance on the visually-guided navigation task only after rTMS is applied to OPA (but not vertex) indicates causal involvement of OPA in visually-guided navigation.

    Time frame: During rTMS of control site and during rTMS of OPA, on Day 1

  4. Reaction Time During Visually-guided Navigation Behavioral-based Task

    To assess performance during the visually-guided navigation behavioral-based task, rTMS is applied to to the control vertex site, which is not implicated in visually-guided navigation, as well as the occipital place area (OPA) site. Participants are asked to complete simple behavioral tasks (e.g., actually walk around a small room and search for hidden objects). Performance is measured as the time (in milliseconds) that it takes to complete the task correctly. A decrease in performance on the visually-guided navigation task only after rTMS is applied to OPA (but not vertex) indicates causal involvement of OPA in visually-guided navigation.

    Time frame: During rTMS of control site and during rTMS of OPA, on Day 1

07

Results

Posted Apr 24, 2025

Participant flow

Participants were recruited at Emory University in Atlanta, Georgia, USA. Participant enrollment began March 3, 2023 and the final study visit occurred May 17, 2023. The study was terminated in February 2025. The study was terminated prior to enrolling participants into the behavioral-based task study arm.

Participant flow — Overall Study
MilestoneRepetitive Transcranial Magnetic Stimulation (rTMS) During Computer-based TaskRepetitive Transcranial Magnetic Stimulation (rTMS) During Behavioral-based Task
Started110
Completed110
Not completed00

Outcome measures

PrimaryAccuracy During Visually-guided Navigation Computer-based Task

To assess performance during the visually-guided navigation computer-based task, rTMS is applied to to the control vertex site, which is not implicated in visually-guided navigation, as well as the occipital place area (OPA) site. While participants are shown simple visual stimuli of places (e.g., bedrooms, kitchens, and living rooms) they are asked to perform simple computer-based tasks (e.g., imagine they are walking through the room, and respond via button press whether they can leave through a door on the left, center, or right wall, as indicated by a continuous path on the floor). Performance is measured in task accuracy (the percentage of tasks performed correctly). A decrease in performance on the visually-guided navigation task only after rTMS is applied to OPA (but not vertex) indicates causal involvement of OPA in visually-guided navigation.

Time frame:
During rTMS of control site and during rTMS of OPA, on Day 1
Reported as:
Mean · percent of task accuracy
Accuracy During Visually-guided Navigation Computer-based Task
percent of task accuracyRepetitive Transcranial Magnetic Stimulation (rTMS) During Computer-based Task
rTMS Control Site80.24 ± 14.62
rTMS Occipital Place Area (OPA)82.44 ± 14.42
PrimaryReaction Time During Visually-guided Navigation Computer-based Task

To assess performance during the visually-guided navigation computer-based task, rTMS is applied to to the control vertex site, which is not implicated in visually-guided navigation, as well as the occipital place area (OPA) site. While participants are shown simple visual stimuli of places (e.g., bedrooms, kitchens, and living rooms) they are asked to perform simple computer-based tasks (e.g., imagine they are walking through the room, and respond via button press whether they can leave through a door on the left, center, or right wall, as indicated by a continuous path on the floor). Performance is measured in the time (in milliseconds) that it takes to complete the task correctly. A decrease in performance on the visually-guided navigation task only after rTMS is applied to OPA (but not vertex) indicates causal involvement of OPA in visually-guided navigation.

Time frame:
During rTMS of control site and during rTMS of OPA, on Day 1
Reported as:
Mean · milliseconds (ms)
Reaction Time During Visually-guided Navigation Computer-based Task
milliseconds (ms)Repetitive Transcranial Magnetic Stimulation (rTMS) During Computer-based Task
rTMS Control Site644.23 ± 120.99
rTMS Occipital Place Area (OPA)660.08 ± 109.22
PrimaryAccuracy During Visually-guided Navigation Behavioral-based Task

To assess performance during the visually-guided navigation behavior-based task, rTMS is applied to to the control vertex site, which is not implicated in visually-guided navigation, as well as the occipital place area (OPA) site. Participants are asked to complete simple behavioral-based tasks (e.g., actually walk around a small room and search for hidden objects). Performance is measured in task accuracy (the percentage of tasks performed correctly). A decrease in performance on the visually-guided navigation task only after rTMS is applied to OPA (but not vertex) indicates causal involvement of OPA in visually-guided navigation.

Time frame:
During rTMS of control site and during rTMS of OPA, on Day 1

No measurements were reported for this outcome.

PrimaryReaction Time During Visually-guided Navigation Behavioral-based Task

To assess performance during the visually-guided navigation behavioral-based task, rTMS is applied to to the control vertex site, which is not implicated in visually-guided navigation, as well as the occipital place area (OPA) site. Participants are asked to complete simple behavioral tasks (e.g., actually walk around a small room and search for hidden objects). Performance is measured as the time (in milliseconds) that it takes to complete the task correctly. A decrease in performance on the visually-guided navigation task only after rTMS is applied to OPA (but not vertex) indicates causal involvement of OPA in visually-guided navigation.

Time frame:
During rTMS of control site and during rTMS of OPA, on Day 1

No measurements were reported for this outcome.

Adverse events

Collected over Information on adverse events was collected during the single study visit (Day 1).. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Repetitive Transcranial Magnetic Stimulation (rTMS) During Computer-based Task0/11 (0%)0/11 (0%)0/11 (0%)

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Repetitive Transcranial Magnetic Stimulation (rTMS) During Computer-based Task
<=18 years0
Between 18 and 65 years11
>=65 years0
Sex: Female, Male
Sex: Female, Male(Participants)Repetitive Transcranial Magnetic Stimulation (rTMS) During Computer-based Task
Female8
Male3
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Repetitive Transcranial Magnetic Stimulation (rTMS) During Computer-based Task
Hispanic or Latino2
Not Hispanic or Latino8
Unknown or Not Reported1
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Repetitive Transcranial Magnetic Stimulation (rTMS) During Computer-based Task
American Indian or Alaska Native0
Asian3
Native Hawaiian or Other Pacific Islander0
Black or African American0
White5
More than one race2
Unknown or Not Reported1
Region of Enrollment
Region of Enrollment(Participants)Repetitive Transcranial Magnetic Stimulation (rTMS) During Computer-based Task
United States11
08

Study locations

1 site
  • Emory University
    Atlanta, Georgia 30322, United States
09

References and documents

Study documents

  • Protocol and statistical analysis plan · Apr 11, 2021
  • Informed consent form · Jun 4, 2024

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 24, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT04961645
Lead sponsor
Emory University
Collaborators
National Eye Institute (NEI)
Responsible party
Daniel Dilks (Associate Professor, Emory University) — Principal investigator
First posted
Jul 14, 2021
Start date
Mar 3, 2023
Primary completion
May 17, 2023
Completion
May 17, 2023
Results posted
Apr 24, 2025
Last update
Apr 24, 2025

Study contacts

Daniel Dilks, PhD
principal investigator · Emory University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion