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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03227406
Other study ID # 2016P000222
Secondary ID R01MH048832
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2016
Est. completion date January 31, 2023

Study information

Verified date February 2023
Source Beth Israel Deaconess Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To further understanding of the relationship between sleep and memory the investigators will address and attempt to answer three questions, (1) how memories evolve across wake and sleep, (2) how different aspects of this memory evolution are reflected both behaviorally and in the EEG signal, and (3) what stages and features of sleep affect memory evolution. Together, these studies will provide a greater breadth and depth of knowledge concerning sleep's role in memory consolidation. Such knowledge would be of practical importance for educational practices, whether in schools, on the job, or in the military, and would also provide valuable information to the fields of sleep medicine and psychiatry, where interactions between sleep disorders and cognitive functioning are of great importance.


Description:

Goal 1: How do memories evolve across wake and sleep? The investigators are interested in how specific memories are selected for change across periods of wake and sleep, and in characterizing the manner in which those memories change. There has been research into broad areas of memory, such as procedural and declarative memory, but other forms of memory, such as semantic memory, remain unexplored, as well as different subtypes of memory within these broad areas. Additionally, it is presently unknown how memories are selected for subsequent processing during sleep and wake. The investigators aim to characterize which memories change, how they are selected, and how they change differently over periods that include sleep versus periods during which participants remain awake. Goal 2: How are these changes reflected behaviorally and in the EEG signal? The investigators will employ and develop specific behavioral and electrophysiological tasks and measures that allow one to probe the state of a particular type of memory and determine how it changes over periods of wake and sleep. EEG signals may be informative about the status of a memory during behavioral performance as well as during both waking and sleeping offline states. Goal 3: What stages and features of sleep affect memory evolution? In the cases in which sleep in particular is found or suspected to influence memories in a unique way, the investigators will assess which stages and features of sleep are involved in that evolution. Generally, this will be accomplished by correlating measures such as time spent in a sleep stage, prominence of particular brain oscillations, or density of spindles with changes in behavior or in other EEG metrics


Recruitment information / eligibility

Status Completed
Enrollment 276
Est. completion date January 31, 2023
Est. primary completion date January 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - willing and able to follow the protocol - willing to refrain from alcohol and recreational drugs for the duration of the protocol - in some cases, English as a first language, normal hearing, and/or normal or corrected to normal vision is required Exclusion Criteria: - self-reported sleep disturbances - a history of mental illness - the use of any drugs that could affect either sleep or cognitive functioning (e.g., sleeping pills or antidepressants)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Sleep deprivation
Subjects are kept awake all night.
Nap
Participants are given a 90-minute nap opportunity in the early afternoon.

Locations

Country Name City State
United States Robert Stickgold Boston Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Beth Israel Deaconess Medical Center National Institute of Mental Health (NIMH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Motor sequence task improvement The increase in the number of correct sequences typed, from the last three training trials to the first three delayed-test trials, is calculated as a percent improvement. 4-24 hrs
Primary Psychomotor vigilance task lapse rate The absolute number of trials in a 5-min test period on which the participant fails to responds with 500ms is calculated as the lapse rate. 4-24 hrs
Primary Serial reaction time test improvement At two time points, separated by a period of wake or sleep, the average reaction time to stimuli in repeated sequence blocks is subtracted from the average reaction time in random blocks. The percent increase in this difference, from the final blocks in the first test to the first blocks in the second test, is calculated as a percent improvement. 4-24 hrs
Primary Visual discrimination task improvement At two time points, separated by a period of wake or sleep, the interpolated stimulus-mask ISI corresponding to 80% accuracy on the texture discrimination task is determined, and task improvement is calculated as the difference between these thresholds, in ms. 4-24 hrs
Secondary Sleep architecture (absolute times) Sleep is recorded with standard polysomnography and the amount of time spent in each wake and sleep stage calculated. 4-24 hrs
Secondary Sleep architecture (percent times) The percent of total sleep time spent in each sleep stage is calculated. 4-24 hrs
Secondary Spindle The density of sleep spindles per minute of N2 sleep is calculated. 4-24 hrs
Secondary Sleep microstructure The EEG spectral power is calculated for N2 and N3 sleep. 4-24 hrs
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