Evidence map›Paper›PMID 27094721›Full record

Trial reportContemporary clinical trials2016

Examining the efficacy of d-cycloserine to augment therapeutic learning in depression.

Michael W Otto, Josephine Lee, Stefan G Hofmann, Bridget A Hearon, Jasper A J Smits, David Rosenfield, Maurizio Fava, Jesse H Wright

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

Trial report in Contemporary clinical trials, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02376257 (Improving Therapeutic Learning in Depression), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 28% 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.

NCT02376257 phase2completednot on this map

Improving Therapeutic Learning in Depression: Proof of Concept

TypeinterventionalSponsorBoston University Charles River CampusRan2014 to 2017Enrolled36ConditionsMajor Depressive DisorderArms250 mg DCS, 100 mg Modafinil, Placebo
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. 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

8 authors at 5 institutions in 1 country.

Michael W OttoDepartment of Psychological and Brain Sciences, Boston University, United States. Electronic address: mwotto@bu.edu.
Josephine LeeDepartment of Psychological and Brain Sciences, Boston University, United States.
Stefan G HofmannDepartment of Psychological and Brain Sciences, Boston University, United States.
Bridget A HearonDepartment of Psychological and Brain Sciences, Boston University, United States.
Jasper A J SmitsInstitute for Mental Health Research and Department of Psychology, University of Texas at Austin, United States.
David RosenfieldDepartment of Psychology, Southern Methodist University, United States.
Maurizio FavaDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, United States.
Jesse H WrightDepartment of Psychiatry and Behavioral Sciences, University of Louisville School of Medicine, United States.
Boston University · USHarvard University · USSouthern Methodist University · USTexas Research Institute · USUniversity of Louisville · US

Funding

2/3-Dose Timing of D-cycloserine to Augment CBT for Social Anxiety DisorderR34MH099311 · NIMH · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI HOFMANN, STEFAN G. · 2014 to 2016
$737k
Improving Therapeutic Learning in Depression: Proof of ConceptR21MH102646 · NIMH · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI OTTO, MICHAEL W. · 2014 to 2015
$452k
AHRQ HHS R18 HS024047NIMH NIH HHS R21 MH102646NIMH NIH HHS R34 MH099311
6 · The paper itself

Abstract

Despite advances in individual and combined treatments for major depression, issues with non-response and partial-response remain relatively common, motivating the search for new treatment strategies. This study aims to develop one such novel treatment. In this proof-of-concept study, we are investigating whether the treatment enhancing effects of d-cycloserine (DCS) administration can be extended outside the extinction-learning paradigms where they have been primarily examined. Using uniform delivery of cognitive behavioral therapy (CBT) content via computer-administered interventions for depression, we are assessing the value of pre-session administrations of DCS for retention of therapeutic learning. Recall of this information is evaluated in conjunction with performance on standardized tests of memory recall with both emotional and non-emotional stimuli. Specifically, in a randomized, double-blind trial we will compare the benefits of two pre-session administrations of DCS augmentation to those achieved by similar administrations of modafinil or placebo. Because modafinil is associated with a number of discriminable effects in addition to cognitive enhancement (e.g., feelings of vigor, alertness, positive mood); whereas these effects would not be expected with DCS, we will assess drug context effects in relation to memory augmentation effects.

Indexed as

LearningAntimetabolitesBenzhydryl CompoundsCognitive Behavioral TherapyCombined Modality TherapyCycloserineDepressive DisorderDouble-Blind MethodHumansMajor Depressive DisorderModafinilNeuropsychological TestsWakefulness-Promoting AgentsAntimetabolitesBenzhydryl CompoundsCycloserineModafinilWakefulness-Promoting AgentsCognitive behavioral therapyd-cycloserineDeclarative memoryDepressionModafinil

Identifiers

PMID27094721
PMCPMC10999219
OpenAlexW2340115664

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.