search
Back to results

Sleep and Emotional Memory in Peripubertal Anxiety

Primary Purpose

Anxiety

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Sleep with Sound Cues
Sleep with Sham Cues
Sponsored by
Florida International University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Anxiety

Eligibility Criteria

10 Years - 13 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 10-13 years old
  • Able to understand and communicate in English and have a parent who is able to understand and communicate in English or Spanish
  • included across any range of symptoms of anxiety, and may meet full diagnostic criteria for Social Phobia, Generalized Anxiety and Separation Anxiety.
  • be right-handed.

Exclusion Criteria:

  • For youth to be excluded from participation, they must:

    1. meet diagnostic criteria for Psychotic Disorders, Major Depressive Disorder, Pervasive Developmental Disorders (including autism spectrum disorders), Obsessive Compulsive Disorder, Conduct Disorder, Bipolar Disorder, Tic disorder, Impulse Control Disorders, or Intellectual Disability.
    2. take medications that affect central nervous system function
    3. show high likelihood and/or serious intent of hurting themselves or others.
    4. have not been living with a primary caregiver for at least 6 months who is legally able to give consent for the child's participation.
    5. be a victim of previously undisclosed abuse requiring investigation or ongoing supervision by the Department of Children and Families.
    6. have a serious vision problem that is not corrected with prescription lenses, or have prescription glasses outside of the range of -5.00 to +3.00 (contact lenses are ok).
    7. have a physical disability that interferes with their ability to lie in scanner and/or click a mouse button rapidly.
    8. have a serious hearing problem.
    9. have a history of neurological or other major medical conditions affecting brain function.
    10. current sleep apnea, and circadian rhythm disturbances (i.e., advanced or delayed sleep-phase)
    11. self-reported average sleep duration < 6 hours or > 11 hours across weekday and weekend nights, or normal bedtime later than 1:00 am.
    12. Are not suitable to undergo MRI scanning due to claustrophobia, certain implanted devices/metal (e.g., cardiac pacemaker, neurostimulator, some artificial joints, metal pins, surgical/aneurysm clips, heart valves, cochlear implants, pregnant, retinal implants, shrapnel in eye, nonremovable body piercing or other non-MRI compatible metal/device, need prescription glasses that are outside of range .

Sites / Locations

  • Center for Children and Families, Florida International UniversityRecruiting
  • Nicklaus Children's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Sleep with Sound Cues

Sleep with Sham Cues

Arm Description

Sounds played at time of memory encoding will be replayed during sleep to cue memory processing.

Sounds that were not played at time of memory encoding will be played during sleep as a sham comparison

Outcomes

Primary Outcome Measures

Object Completion Memory Task (behavioral and fMRI)
Reporting "old" versus "new" in response to a picture set that includes old, new and similar pictures to those learned at baseline in order to capture metrics of memory generalization (pattern completion).

Secondary Outcome Measures

Object Completion Memory Task (behavioral and fMRI)
Reporting "old" versus "new" in response to a picture set that includes old, new and similar pictures to those learned at baseline in order to capture metrics of memory generalization (pattern completion).

Full Information

First Posted
July 19, 2018
Last Updated
March 29, 2023
Sponsor
Florida International University
search

1. Study Identification

Unique Protocol Identification Number
NCT03643848
Brief Title
Sleep and Emotional Memory in Peripubertal Anxiety
Official Title
Sleep-dependent Negative Overgeneralization in Peri-pubertal Anxiety
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 1, 2018 (Actual)
Primary Completion Date
February 28, 2024 (Anticipated)
Study Completion Date
February 28, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Florida International University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The current study aims to deepen understanding of the symptom dimension of negative overgeneralization in anxiety. Specifically, the study examines the malleability of memory processes that are known to occur during sleep that may underlie negative overgeneralization.
Detailed Description
Up to 50% of peripubertal youth with anxiety have unmet clinical needs, leaving these youth at high risk for suicide, depression and substance abuse across adolescence. In accord with the NIMH strategic plan, the proposal aims to deepen mechanistic understanding of anxiety during the sensitive period of peripuberty to inform novel treatments and reduce health risks. The focus is on negative overgeneralization, which is a core dimension of anxiety that is poorly understood, and refers to the tendency to generalize aversive responses from one context (house fire) to other contexts (camp-fire) that share features. Amygdala activity, induced by heightened emotional arousal, enhances plasticity in associative learning mechanisms, facilitating the binding of contextual features in memory that are only loosely related. The proposal posits that sleep plays a critical role in negative overgeneralization. Specifically, the proposal draws from basic neuroscience to posit a model by which heightened amygdala reactivity during wakefulness, induced by increased emotional arousal, facilitates replay of negative memories during sleep. This facilitated replay leads to the stabilization and integration (consolidation) of negative memories into long-term memory networks via slow wave oscillatory events during NREM sleep. The proposal further posits that facilitated replay of negative memories during sleep promotes generalization by influencing underlying neurocomputational mechanisms (i.e., pattern completion - a computational process that makes neural representations similar). Finally, the proposal posits that sleep-dependent consolidation is malleable, such that Targeted Memory Reactivation (TMR) of positive memories during sleep can competitively displace consolidation of negative memories. This model is tested using a novel multi-method approach combining neuroimaging, polysomnography, and a memory task that captures behavioral generalization and its underlying neural mechanisms (i.e. pattern completion). Aims 1 and 2 do not involve a clinical trial. Aim 1 examines 200 peripubertal youth (ages 10-13 years) across a full continuum of anxious symptoms in a randomized sleep (n=140) versus wake (n=60) design to demonstrate sleep-dependent effects on behavioral and neural mechanisms of negative overgeneralization. Aim 2 focuses on the 140 youth in the sleep condition to evaluate amygdala reactivity at encoding and sleep neurophysiology during post-encoding sleep as mediators between anxiety and negative overgeneralization. Aim 3 is the clinical trial to which this registration refers. In Aim 3, the same design as the sleep condition (above) is used, but a new sample of youth with elevated anxiety (n=60) is recruited to enroll in a randomized trial in which positive memories are cued during sleep (TMR, n=30), or sham cues are presented during sleep (n=30), to examine malleability of sleep-dependent mechanisms of negative overgeneralization. This project will set the stage for the long-term goal of developing novel interventions that manipulate sleep (e.g. via TMR) not only to improve existing symptoms, but also to positively shape neurodevelopment and reduce risk in the sensitive period of peripuberty.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Per NIMH policy at the time of funding, the current trial is considered a clinical trial due to prospective, randomized assignment to an "intervention" to observe effects on behavioral or health related outcomes. The "intervention" for Aim 3 (n=60) includes randomized assignment to sham sounds (sounds unrelated to the memory task) or target sounds (sounds that were played during the time of the memory task) that are played during sleep to cue memory processing.
Masking
ParticipantOutcomes Assessor
Masking Description
Double blind (participant, outcome assessor) for Aim 3 (sham versus target sounds)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sleep with Sound Cues
Arm Type
Experimental
Arm Description
Sounds played at time of memory encoding will be replayed during sleep to cue memory processing.
Arm Title
Sleep with Sham Cues
Arm Type
Sham Comparator
Arm Description
Sounds that were not played at time of memory encoding will be played during sleep as a sham comparison
Intervention Type
Behavioral
Intervention Name(s)
Sleep with Sound Cues
Intervention Description
Experimental manipulation to observe effects on memory for learned material.
Intervention Type
Behavioral
Intervention Name(s)
Sleep with Sham Cues
Intervention Description
Sham manipulation
Primary Outcome Measure Information:
Title
Object Completion Memory Task (behavioral and fMRI)
Description
Reporting "old" versus "new" in response to a picture set that includes old, new and similar pictures to those learned at baseline in order to capture metrics of memory generalization (pattern completion).
Time Frame
Delayed recall, 1 week
Secondary Outcome Measure Information:
Title
Object Completion Memory Task (behavioral and fMRI)
Description
Reporting "old" versus "new" in response to a picture set that includes old, new and similar pictures to those learned at baseline in order to capture metrics of memory generalization (pattern completion).
Time Frame
Recall, 12 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 10-13 years old Able to understand and communicate in English and have a parent who is able to understand and communicate in English or Spanish included across any range of symptoms of anxiety, and may meet full diagnostic criteria for Social Phobia, Generalized Anxiety and Separation Anxiety. be right-handed. Exclusion Criteria: For youth to be excluded from participation, they must: meet diagnostic criteria for Psychotic Disorders, Major Depressive Disorder, Pervasive Developmental Disorders (including autism spectrum disorders), Obsessive Compulsive Disorder, Conduct Disorder, Bipolar Disorder, Tic disorder, Impulse Control Disorders, or Intellectual Disability. take medications that affect central nervous system function show high likelihood and/or serious intent of hurting themselves or others. have not been living with a primary caregiver for at least 6 months who is legally able to give consent for the child's participation. be a victim of previously undisclosed abuse requiring investigation or ongoing supervision by the Department of Children and Families. have a serious vision problem that is not corrected with prescription lenses, or have prescription glasses outside of the range of -5.00 to +3.00 (contact lenses are ok). have a physical disability that interferes with their ability to lie in scanner and/or click a mouse button rapidly. have a serious hearing problem. have a history of neurological or other major medical conditions affecting brain function. current sleep apnea, and circadian rhythm disturbances (i.e., advanced or delayed sleep-phase) self-reported average sleep duration < 6 hours or > 11 hours across weekday and weekend nights, or normal bedtime later than 1:00 am. Are not suitable to undergo MRI scanning due to claustrophobia, certain implanted devices/metal (e.g., cardiac pacemaker, neurostimulator, some artificial joints, metal pins, surgical/aneurysm clips, heart valves, cochlear implants, pregnant, retinal implants, shrapnel in eye, nonremovable body piercing or other non-MRI compatible metal/device, need prescription glasses that are outside of range .
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Project Coordinator
Phone
305-348-5384
Email
remedy@fiu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dana McMakin, PhD
Organizational Affiliation
Florida International University and Nicklaus Children's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Aaron Mattfeld, PhD
Organizational Affiliation
Florida International University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Center for Children and Families, Florida International University
City
Miami
State/Province
Florida
ZIP/Postal Code
33199
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Project Coordinator
Phone
305-348-5384
Email
dmcmakin@fiu.edu
First Name & Middle Initial & Last Name & Degree
Dana McMakin, PhD
First Name & Middle Initial & Last Name & Degree
Aaron Mattfeld, PhD
Facility Name
Nicklaus Children's Hospital
City
Miami
State/Province
Florida
ZIP/Postal Code
33199
Country
United States
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
yes, data are shared via NIH NDA and include behavioral, imaging, polysomnography and clinical data.

Learn more about this trial

Sleep and Emotional Memory in Peripubertal Anxiety

We'll reach out to this number within 24 hrs