Evidence map›Paper›PMID 23098672›Full record

Trial reportJournal of psychiatric research2013

Augmentation of exposure therapy with post-session administration of D-cycloserine.

Candyce D Tart, Pamela R Handelsman, Lindsey B Deboer, David Rosenfield, Mark H Pollack, Stefan G Hofmann, Mark B Powers, Michael W Otto, Jasper A J Smits

Registry-linked trialOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of psychiatric research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01102803 (Evaluation of the Effects of Post-Session Administration of D-cycloserine On Exposure Therapy Outcomes), which is not on this map. Cited by 33 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 5 pooled it
11.3field-weighted citation impact, top 1% 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.

NCT01102803 phase3completednot on this map

Evaluation of the Effects of Post-Session Administration of D-cycloserine On Exposure Therapy Outcomes

TypeinterventionalSponsorSouthern Methodist UniversityRan2010 to 2011Enrolled40ConditionsPhobic DisordersArmsIndividual Cognitive Behavioral Therapy (CBT), D-Cycloserine, Placebo
3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 5 syntheses or guidelines pooled it, 75 citations in OpenAlex.

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  15. Extinction-Based Exposure Therapies Using Virtual Reality.Current topics in behavioral neurosciences · 2023
    Review
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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

9 authors at 3 institutions in 1 country.

Candyce D TartDepartment of Psychology, Southern Methodist University, USA. candycetart@gmail.com
Pamela R Handelsman
Lindsey B Deboer
David Rosenfield
Mark H Pollack
Stefan G Hofmann
Mark B Powers
Michael W Otto
Jasper A J Smits
Southern Methodist University · USBoston University · USRush University Medical Center · US

Funding

D-Cycloserine Enhancement of Exposure in Social PhobiaR01MH075889 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI POLLACK, MARK H · 2007 to 2010
$1.8M
NIMH NIH HHS R01 MH075889NIMH NIH HHS R01MH075889
6 · The paper itself

Abstract

backgroundPre-session administration of d-cycloserine (DCS) has been found to augment exposure therapy outcomes in a variety of anxiety disorders. To be able to enhance learning only for successful exposure sessions, it would be beneficial to have the option of administering DCS after rather than before the session, a strategy encouraged by pre-clinical work. We believe the present study is the first published report on the efficacy of post-session administration of DCS in humans.

methodAdults (N = 29) with a DSM-IV diagnosis of acrophobia were randomized to receive two sessions of virtual reality exposure therapy (VRE) in combination with placebo or 50 mg of DCS. Instead of administering the pill prior to each of the sessions, as has been done in extant work, we administered the pill immediately following each session. Measures of acrophobia severity were collected at baseline, at each treatment session, 1-week post-treatment, and at 1-month follow-up.

resultsMixed-effects repeated-measures ANOVAs and GLMMs revealed significant improvement in all outcome measures over time, but no between-group differences were observed. At post-treatment, 63.5% of patients in the placebo condition vs. 60.0% of those in the DCS condition were in remission. At 1-month follow up, 63.4% of those in the placebo condition vs. 66.6% of those in the DCS condition were in remission.

conclusionsThese findings do not support the application of post-session DCS administration for augmenting the efficacy of exposure-based treatments. Possible reasons for these findings are discussed. TRIAL REGISTRY: The Trial is registered at ClinicalTrials.gov (NCT01102803).

Indexed as

AdolescentAdultAgedAnalysis of VarianceAntimetabolitesAvoidance LearningCycloserineFemaleHumansImplosive TherapyMaleMiddle AgedNeuropsychological TestsPhobic DisordersPsychiatric Status Rating ScalesSurveys and QuestionnairesAntimetabolitesCycloserine

Identifiers

PMID23098672
PMCPMC3732105
OpenAlexW2049480064

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.