Evidence map›Paper›PMID 24935082›Full record

Trial reportThe American journal of psychiatry2014

Sequential treatment with fluoxetine and relapse--prevention CBT to improve outcomes in pediatric depression.

Betsy D Kennard, Graham J Emslie, Taryn L Mayes, Paul A Nakonezny, Jessica M Jones, Aleksandra A Foxwell, Jessica King

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

Trial report in The American journal of psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00612313 (Pediatric MDD), which is not on this map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
8.6field-weighted citation impact, top 2% 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.

NCT00612313 nacompletednot on this map

Pediatric MDD: Sequential Treatment With Fluoxetine and Relapse Prevention

TypeinterventionalSponsorUniversity of Texas Southwestern Medical CenterRan2008 to 2014Enrolled144ConditionsDepressionArmsFluoxetine, Relapse prevention cognitive behavioral therapy (CBT)
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 134 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Well-Being Therapy for Depression.Advances in experimental medicine and biology · 2024
    Review
  14. [The German S3 guideline for depressive disorders in childhood and adolescence: new developments].Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2023
    Review
  15. Article
  16. Article
  17. Review
  18. Neurocognitive and functional heterogeneity in depressed youth.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Article
  19. Well-being Therapy in Depressive Disorders.Advances in experimental medicine and biology · 2021
    Review
  20. The pursuit of euthymia.World psychiatry : official journal of the World Psychiatric Association (WPA) · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Betsy D Kennard
Graham J Emslie
Taryn L Mayes
Paul A Nakonezny
Jessica M Jones
Aleksandra A Foxwell
Jessica King
Children's Medical Center · USClinical Research Management · USThe University of Texas Southwestern Medical Center · US

Funding

Pediatric MDD: Sequential Treatment with Fluoxetine and Relapse Prevention CBTR01MH039188 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI EMSLIE, GRAHAM J., KENNARD, BETH D · 1986 to 2012
$4.7M
NIMH NIH HHS R01 MH039188NIMH NIH HHS R01 MH39188
6 · The paper itself

Abstract

objectiveThe authors evaluated a sequential treatment strategy of fluoxetine and relapse-prevention cognitive-behavioral therapy (CBT) to determine effects on remission and relapse in youths with major depressive disorder.

methodYouths 8-17 years of age with major depression were treated openly with fluoxetine for 6 weeks. Those with an adequate response (defined as a reduction of 50% or more on the Children's Depression Rating Scale-Revised [CDRS-R]) were randomly assigned to receive continued medication management alone or continued medication management plus CBT for an additional 6 months. The CBT was modified to address residual symptoms and was supplemented by well-being therapy. Primary outcome measures were time to remission (with remission defined as a CDRS-R score of 28 or less) and rate of relapse (with relapse defined as either a CDRS-R score of 40 or more with a history of 2 weeks of symptom worsening, or clinical deterioration).

resultsOf the 200 participants enrolled in acute-phase treatment, 144 were assigned to continuation treatment with medication management alone (N=69) or medication management plus CBT (N=75). During the 30-week continuation treatment period, time to remission did not differ significantly between treatment groups (hazard ratio=1.26, 95% CI=0.87, 1.82). However, the medication management plus CBT group had a significantly lower risk of relapse than the medication management only group (hazard ratio=0.31, 95% CI=0.13, 0.75). The estimated probability of relapse by week 30 was lower with medication management plus CBT than with medication management only (9% compared with 26.5%).

conclusionsContinuation-phase relapse-prevention CBT was effective in reducing the risk of relapse but not in accelerating time to remission in children and adolescents with major depressive disorder.

Indexed as

Cognitive Behavioral TherapyAdolescentChildCombined Modality TherapyFemaleFluoxetineHumansMajor Depressive DisorderMaleRecurrenceRemission InductionTime FactorsFluoxetine

Identifiers

PMID24935082
PMCPMC4182111
OpenAlexW2050645823

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.