Die Dynamik des repräsentativen Wandels, der dem Abruf zugrunde liegt
Die Dynamik repräsentationalen Wandels als Grundlage des Erinnerns
The goal of this clinical trial is to examine how repeated memory retrieval changes visual representations in the brain in healthy adult participants. Specifically, the study aims to determine whether repeated recall strengthens or transforms neural representations in visual cortex compared to a time-matched control condition. The main questions it aims to answer are: 1) Does repeated retrieval produce cumulative changes in visual cortical representations compared to a control condition matched for elapsed time? 2) Do these representational changes differ for simple spatial stimuli and complex natural images?
Researchers will compare neural activity patterns during repeated retrieval to those during a control retrieval condition to determine whether repeated recall leads to systematic changes in representational structure beyond those attributable to the passage of time. Participants will: 1) complete two fMRI sessions. 2) Undergo a localizer session including anatomical imaging, population receptive field (pRF) mapping, and a visual category localizer task. 3) Study cue-stimulus pairs consisting of either simple spatial patterns or natural images. 4) Recall previously studied stimuli multiple times during repeated and control retrieval conditions while undergoing fMRI scanning. Brain activity patterns during study and recall will be compared to assess how repeated retrieval influences the structure and tuning of visual representations.
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Detaillierte Beschreibung
Two fMRI sessions will be conducted per subject. In the localizer session, the investigators will collect anatomical images and fMRI data necessary to define visual areas in each individual's native brain space. In addition to two high-resolution anatomical images, two short functional tasks will be acquired from every participant: 1) population receptive field (pRF) mapping; 2) visual category localizer. The pRF mapping task will be several runs of a bar aperture drifting across the central 8 degrees of the visual field. This will allow us to estimate the retinotopic sensitivity of individual voxels in visual cortex and draw boundaries between different retinotopic field maps. The visual category localizer will be a block design with different image categories. This will allow us to define higher-level category-selective brain areas.
In the experimental session, the investigators will collect fMRI data while subjects are undergoing perception and recall of the same stimuli. In order to assess whether our findings generalize across simple and complex visual stimuli, two classes of stimuli will be used: simple patterns in discrete spatial locations, following previous work, and natural images. In study blocks, subjects will study cue-stimulus pairs. Colored fixation dots will be used as cues. Stimuli will be from one of the aforementioned classes. In recall blocks, participants will be asked to recall the stimulus given the cue. Recall will happen under one of two conditions: repeated and control. The repeated condition allows us to examine how memory representations evolve with repeated retrieval, while the control condition will provide a matched baseline to assess changes over the same true time interval. For pairs in the repeated condition, participants will recall each stimulus 5 times, interleaved with recalls from other pairs. For pairs in the control condition, participants will recall each stimulus 2 times. Critically, recalls from this condition will be spaced such that they are matched to recalls 1 and 5 from the repeated condition, providing a control for elapsed time. Study and recall blocks will be performed in interleaved order.
Analyses will compare BOLD activity patterns from repeated retrieval, control retrieval, and study conditions. Data from study trials will be averaged to form a single pattern for each stimulus. Retrieval data will be analyzed separately for each stimulus and retrieval attempt in both conditions. For both spatial stimuli and natural images, the investigators will focus on comparing representational changes between repeated and control conditions. Although the specific models used to characterize brain representations differ by stimulus type, the analyses will otherwise follow parallel procedures. For spatial stimuli, the investigators will use a previously published approach that combines pRF estimates with task-based BOLD data to quantify spatial tuning in visual areas. This method assesses the amplitude of the task-evoked BOLD response in each voxel as a function of the distance between the voxel's pRF and the spatial location of the stimulus. The investigators will compare spatial tuning across repeated and control retrieval conditions, as well as with the study condition, to determine whether changes in spatial tuning accumulate over repeated retrieval. For natural images, the investigators will compare the representational structure of BOLD activity patterns to that of a convolutional neural network (CNN) model. Using representational similarity analysis (RSA), the investigators will assess the similarity between CNN-derived embeddings and BOLD activity patterns during both study and recall. Higher correlations with early CNN layers suggest that low-level visual features are represented, while higher correlations with deeper layers indicate the representation of higher-level visual features. The investigators will use this approach to compare correlations from the repeated and control conditions, testing whether representational changes strengthen with repeated retrieval.
Studientyp
Studientyp
Einschreibung (Tatsächlich)
Einschreibung
Phase
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
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-
Rhode Island
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Providence, Rhode Island, Vereinigte Staaten, 02906
- Brown University Magnetic MRI Research Facility
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-
Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Exclusion Criteria:
- Under the age of 18 or over the age of 40
- Does not live in the United States or is not a native speaker of English
- Diagnosis of a neurological disorders, a history of head trauma, or diagnosis of psychiatric disorder
- Imperfect and uncorrected visual acuity, color blindness, or imperfect hearing
- Magnetically or mechanically activated implants or other untested metal implants
- Claustrophobia
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Grundlegende Wissenschaft
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
|---|---|
|
Experimental: Experimental Memory Retrieval Task
All participants will complete a visual memory encoding and retrieval task during fMRI scanning. The study uses a within-subject design in which each participant completes both a repeated retrieval condition and a time-matched control retrieval condition. This design allows comparison of neural representational changes associated with repeated retrieval while controlling for elapsed time. |
Participants will study cue-stimulus associations and subsequently retrieve the associated stimuli while undergoing fMRI scanning. Retrieval will occur under two conditions: (1) repeated retrieval, in which stimuli are recalled five times, and (2) control retrieval, in which stimuli are recalled twice with timing matched to the repeated condition. Neural activity patterns during study and recall will be measured using BOLD fMRI. |
Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Representational Change in Visual Cortex
Zeitfenster: 1 hour
|
Difference in multivoxel BOLD activity patterns in visual cortex between repeated and control retrieval conditions during fMRI. |
1 hour
|
Mitarbeiter und Ermittler
Sponsor
Sponsor
Mitarbeiter
Mitarbeiter
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Studienbeginn
Primärer Abschluss (Tatsächlich)
Primärer Abschluss
Studienabschluss (Tatsächlich)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- STUDY00000849
- 5P30GM149405 (US NIH Stipendium/Vertrag)
Plan für individuelle Teilnehmerdaten (IPD)
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Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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