The Effects of Direct Context Reactivation During Sleep on Memory

January 10, 2022 updated by: Eitan Schechtman-Drayman, Northwestern University

The Role of Context in Sleep-related Memory Reactivation in Humans: the Effects of Direct Context Reactivation During Sleep on Memory

The context in which memories are encoded is a major factor influencing how memories are organized. Individual memories are bound to the context (e.g., the location, time and state of mind in which they are encoded) and this context is later reinstated to recall the details related to the memory. Although the role of context has been explored with regard to memory encoding and retrieval, its role during sleep-related memory consolidation has not been explored. Memories are thought to be reactivated during sleep, subsequently benefitting from the process. This study will use encephalography (EEG) in humans to consider several competing hypotheses regarding context's role in sleep reactivation, thereby enhancing the current understanding of how reactivation of memory over sleep relates to models of context and memory. Participants will learn to associate pictures of scenes to different sounds and to smaller images of items and animals, and then learn the spatial locations of these smaller images on a grid. Crucially, for half of these scenes, the sounds themselves will then also be linked directly to some of images during training. The associated sounds will then be unobtrusively presented during sleep, in a manner that has been shown to improve associated memories. The subsequent memory benefits will reveal whether (1) all images associated with the cued scene will benefit from cuing, demonstrating a context-reactivation effect; (2) only the images directly associated with presented sound will benefit from the cuing, demonstrating a item-reactivation effect; or (3) some composite of these two models. Regardless of which hypothesis is correct, the results will expand our current understanding regarding the role context plays in sleep consolidation.

Study Overview

Status

Completed

Conditions

Detailed Description

Each participant will be run in a single afternoon, which includes a 90-minute nap opportunity. Before the nap, participants will go through training and test sessions - and after it they will partake of final memory tests. Neural activity will be continuously monitored and recorded throughout the task using electrophysiological equipment.

This is a within-subjects study. The main manipulation is the unobtrusive presentation of sounds during sleep, a technique called targeted memory reactivation (TMR). All participants will hear these sounds, but the specific sounds each one will hear will be different. The results will then be compared within participant, not between different groups or individuals. Appropriate statistical methods for such analyses include paired t-test and repeated measures analysis of variance. The choice of which sounds will be presented to each participant will be made based on their performance in the pre-sleep test. This will be done in an attempt to balance pre-sleep scores between presented and unpresented stimuli to remove statistical noise. Both the participant and the experimenter will be blind to which sounds will be presented, and the selection will be automatically made by the computer. This technique has been extensively used and has no known risks.

There are two main reasons that using a within-subject design reduces the required sample size. First, the lack of a between-subject independent variable intuitively requires less participants. Second, the level of statistical noise due to individual differences is reduced (i.e., because each participant is compared with their own scores). Previous TMR studies, which have found significant cuing effects, commonly used 20-25 participants. I plan to include at least 30 participants in this study, after omitting participants who could not complete the task and those who were not sufficiently cued during sleep. Having 30 participants will allow the use of more powerful statistical methods (in accordance with the common rule of thumb derived from the central limit theorem, which states that means based on sample sizes of more than 30 participants can be assumed to follow a normal distribution). I expect the context-related TMR effect (see summary) to be smaller in magnitude relative to the common effect size observed in spatial learning TMR studies (Hedge's g = 0.39 based on a recent meta-analysis). This is why I included a higher sample size. It is important to note that even if this benefit will be of a smaller magnitude, as I expect, it will still be indicative of the underlying neurocognitive process and therefore extremely valuable for our mechanistic understanding of the role of context in sleep. Aiming at a sample size of at least 30 participants and assuming an omission rate of 80%, I therefore plan to have 38 participants altogether.

Here is a brief summary of the procedure:

Stimuli: 16 images of spatial scenes (e.g., a beach) will each be arbitrarily associated with a sound and with four smaller images of objects or animals. Half of the scenes will be randomly designated to the context-reactivation (CR) condition and half to the item-reactivation (IR) condition (see below). The 64 images will each have a unique 2D position on a circular grid presented on the screen.

Training: Participants will first learn to associate each scene with the paired sound up to criterion. Next, they will learn to associate the scene with its four images up to criterion. The last part of training will include two type of learning blocks that will be interspersed. During the spatial-training blocks, in each trial participants will have to place a single image in its correct location. They will then receive feedback to improve. The scene associated with the image will be presented while they learn, but crucially the sound will never be presented for the CR condition scenes. For the IR scenes, the sound will be presented while learning two of the items, but never for the other two.

An alternative design might have divorced the cued items in the CR condition from the scenes altogether; the items could have been associated with novel sounds (i.e., that were not connected to the scene) and not presented along with their scene. However, using such a design would have introduced a confounding factor. The novel sound may have still been associated, to an unknown degree, not only to the item but also to the context to which it belongs. The degree to which this novel sound would be associated with the context would therefore remain uncontrolled and may vary between participants and scenes. Sounds used for item in the IR condition are always additionally associated with the scene. By always having the sounds be associated both with context and - in the IR condition - additionally to items, I substantially reduce any interpretation issues.

During the Sound-scenes blocks, which do not include a spatial component or the smaller images at all, the scenes will be presented with the sounds only for the CR condition scenes (i.e., to balance the number of sound presentations between conditions). These blocks will repeat in an interleaved manner until each participant will reach the pre-set learning criterion on the spatial-task.

Pre-sleep test: After training, participants will be tested on their spatial-memory for all items without exposure to sounds or scenes.

Sleep: During NREM (non-rapid eye movement) sleep, the sounds associated with half of the CR condition scenes and half of the IR condition scenes will be presented unobtrusively. The choice of which sounds to present will be made in a manner that will balance pre-sleep results and therefore enhance the contrast between sleep-related effects for cued and non-cued images.

Post-sleep test: At least 10 minutes after the end of the nap, participants will undergo a test identical to the pre-sleep one. Immediately after, they will be tested on the scene-item and scene-sound associations using both a free-recall and a recognition test. Participants will then be thanked, debriefed, paid and dismissed.

Study Type

Interventional

Enrollment (Actual)

38

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Illinois
      • Evanston, Illinois, United States, 60208
        • Cognitive Neuroscience Lab - Northwestern University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

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Exclusion Criteria:

Participants with a history of neurological disorders or of sleep disorders will be excluded.

Participants who do not believe they would be able to fall asleep in the lab will be excluded.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental group
This is a within-subject study with a single group of participants
I will unobtrusively and repeatedly present learning-related sounds during sleep using speakers. This method was shown to improve memory in various tasks. The sounds will be presented several seconds apart and the volume will be so adjusted as not to disturb the participant's sleep. The sounds will be presented during non-rapid eye movement sleep (sleep stage 2 and slow wave sleep). The sounds presented will be non-congruently related to the scenes in the previous learning task. This manipulation is within-subject - all participants will get it, but different specific sounds will be presented for each individual participant.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in error rates between pre- and post-sleep for the different conditions
Time Frame: Approximately 15 minutes before sleep onset and approximately 15 minutes after sleep offset within the same experimental session
The correct location of an image is compared with the position in which the participant has placed it. Measured in pixels on a computer screen.
Approximately 15 minutes before sleep onset and approximately 15 minutes after sleep offset within the same experimental session
Modulation of EEG spectral power following sound/odor presentation
Time Frame: During sleep within the experimental session, assessed up to 1.5 hours
Power modulations within the sigma (12-16 Hz), theta (4-8 Hz) and delta (0.5-4 Hz) ranges immediately following sound onset. Measured across different EEG channels.
During sleep within the experimental session, assessed up to 1.5 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 15, 2020

Primary Completion (Actual)

November 30, 2021

Study Completion (Actual)

November 30, 2021

Study Registration Dates

First Submitted

January 6, 2021

First Submitted That Met QC Criteria

January 7, 2021

First Posted (Actual)

January 8, 2021

Study Record Updates

Last Update Posted (Actual)

January 12, 2022

Last Update Submitted That Met QC Criteria

January 10, 2022

Last Verified

January 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • STU00213443-A

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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