Evidence map›Paper›PMID 30340182›Full record

Trial reportPsychiatry research2018

Effects of post-exposure naps on exposure therapy for social anxiety.

Edward F Pace-Schott, Ryan M Bottary, Se-Yun Kim, Peter L Rosencrans, Shilpa Vijayakumar, Scott P Orr, Natasha B Lasko, Elizabeth M Goetter, Amanda W Baker, Matt T Bianchi and 4 more

3 registry-linked trialsAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Psychiatry research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.7field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02325128 nacompletednot on this map

Augmentation of Exposure Therapy for High Levels of Social Anxiety Using Post-exposure Naps

TypeinterventionalSponsorMassachusetts General HospitalRan2015 to 2016Enrolled35ConditionsSocial Anxiety Disorder, Sleep LaboratoryArmsSleep-enhancement of extinction memory
NCT05663151 narecruitingnot on this mapstarted 2024, after this paper: background citation

Mechanisms Underlying the Efficacy of Prolonged Exposure

TypeinterventionalSponsorVA Boston Healthcare SystemRan2024 to 2027Enrolled50ConditionsPosttraumatic Stress DisorderArmsProlonged Exposure Therapy for Posttraumatic Stress Disorder
NCT05788302 narecruitingnot on this mapstarted 2023, after this paper: background citation

Mechanisms Underlying Efficacy of Prolonged Exposure

TypeinterventionalSponsorMassachusetts General HospitalRan2023 to 2027Enrolled50ConditionsPost Traumatic Stress DisorderArmsProlonged Exposure
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 42 citations in OpenAlex.

  1. Trial
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  3. Trial
  4. Review
  5. Article
  6. Article
  7. Comparison of autonomic reactivity to trauma and nightmare imagery: A Pilot Study.Sleep advances : a journal of the Sleep Research Society · 2024
    Article
  8. Neurocognitive Model of Schema-Congruent and -Incongruent Learning in Clinical Disorders: Application to Social Anxiety and Beyond.Perspectives on psychological science : a journal of the Association for Psychological Science · 2023
    Article
  9. The Impact of Sleep on Fear Extinction.Current topics in behavioral neurosciences · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. The role of sleep in fear learning and memory.Current opinion in psychology · 2020
    Review
  17. Article
  18. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 1 country.

Edward F Pace-SchottDepartment of Psychology, University of Washington, Seattle, WA, USA. Electronic address: epace-schott@mgh.harvard.edu.
Ryan M BottaryDepartment of Psychology, University of Washington, Seattle, WA, USA; Department of Psychology, Boston College, Chestnut Hill, MA, USA.
Se-Yun KimDepartment of Psychology, University of Washington, Seattle, WA, USA.
Peter L RosencransDepartment of Psychology, University of Washington, Seattle, WA, USA.
Shilpa VijayakumarDepartment of Psychology, University of Washington, Seattle, WA, USA.
Scott P OrrDepartment of Psychology, University of Washington, Seattle, WA, USA.
Natasha B LaskoDepartment of Psychology, University of Washington, Seattle, WA, USA.
Elizabeth M GoetterDepartment of Psychology, University of Washington, Seattle, WA, USA.
Amanda W BakerDepartment of Psychology, University of Washington, Seattle, WA, USA.
Matt T BianchiDepartment of Neurology, Harvard Medical School, Massachusetts General Hospital, Boston, MA, USA.
Karen GannonDepartment of Neurology, Harvard Medical School, Massachusetts General Hospital, Boston, MA, USA.
Susanne S HoeppnerDepartment of Psychology, University of Washington, Seattle, WA, USA.
Stefan G HofmannDepartment of Psychological and Brain Sciences, Boston University, Boston, MA, USA.
Naomi M SimonDepartment of Psychology, University of Washington, Seattle, WA, USA; Department of Psychiatry, NYU School of Medicine, New York, NY, USA.
University of Washington · USHarvard University · USBoston College · USBoston University · US

Funding

Augmentation of exposure therapy for high levels of social anxiety using post-exposure napsR21MH103484 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI PACE-SCHOTT, EDWARD F. · 2014 to 2015
$479k
NIMH NIH HHS R21 MH103484
6 · The paper itself

Abstract

Exposure therapy for social anxiety disorder (SAD) utilizes fear extinction, a memory process enhanced by sleep. We investigated whether naps following exposure sessions might improve symptoms and biomarkers in response to social stress in adults undergoing 5-week exposure-based group SAD therapy. Thirty-two participants aged 18-39 (18 females) with SAD were randomized. Before and after treatment, participants completed the Liebowitz Social Anxiety Scale (LSAS) and underwent a Trier Social Stress Test with psychophysiological monitoring (mpTSST) that included skin conductance (SCL), electromyographic (EMG) and electrocardiographic recording, and an auditory startle procedure while anticipating the social stressor. At sessions 3 and 4, exposure was followed by either a 120-min polysomnographically monitored sleep opportunity (Nap, N = 17) or wakefulness (Wake, N = 15). Primary hypotheses about SAD symptom change (LSAS) and EMG blink-startle response failed to differ with naps, despite significant symptom improvement (LSAS) with therapy. Some secondary biomarkers, however, provided preliminary support for enhanced extinction learning with naps, with trend-level Time (pre-, post-treatment) × Arm interactions and significant reduction from pre- to post treatment in the Nap arm alone for mpTSST SCL and salivary cortisol rise. Because of the small sample size and limited sleep duration, additional well-powered studies with more robust sleep interventions are indicated.

Indexed as

AdolescentAdultFemaleHumansHydrocortisoneImplosive TherapyMaleMiddle AgedPhobia, SocialPolysomnographyPsychotherapy, GroupSalivaSleepTreatment OutcomeWakefulnessYoung AdultHydrocortisoneCortisolExposure therapyExtinctionPsychophysiologySleepSocial anxiety disorder

Identifiers

PMID30340182
PMCPMC6292728
OpenAlexW2896820795

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.