Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2006 Jul;63(7):749-55.
doi: 10.1001/archpsyc.63.7.749.

Cognitive reactivity to sad mood provocation and the prediction of depressive relapse

Affiliations
Randomized Controlled Trial

Cognitive reactivity to sad mood provocation and the prediction of depressive relapse

Zindel V Segal et al. Arch Gen Psychiatry. 2006 Jul.

Erratum in

  • Errors in Text and Table.
    [No authors listed] [No authors listed] JAMA Psychiatry. 2023 Jan 1;80(1):96. doi: 10.1001/jamapsychiatry.2022.3972. JAMA Psychiatry. 2023. PMID: 36416854 Free PMC article. No abstract available.

Abstract

Context: Episode remission in unipolar major depression, while distinguished by minimal symptom burden, can also be a period of marked sensitivity to emotional stress as well as an increased risk of relapse.

Objective: To examine whether mood-linked changes in dysfunctional thinking predict relapse in recovered patients who were depressed.

Design: In phase 1 of this study, patients with major depressive disorder were randomly assigned to receive either antidepressant medication or cognitive behavior therapy. In phase 2, patients who achieved clinical remission underwent sad mood provocation and were then observed with regular clinical assessments for 18 months.

Setting: Outpatient psychiatric clinics at the Centre for Addiction and Mental Health, Toronto, Ontario.

Participants: A total of 301 outpatients with major depressive disorder, aged 18 to 65 years, participated in phase 1 of this study and 99 outpatients with major depressive disorder in remission, aged 18 to 65 years, participated in phase 2.

Main outcome measure: Occurrence of a relapse meeting DSM-IV criteria for a major depressive episode as assessed by the longitudinal interval follow-up evaluation and a Hamilton Depression Rating Scale score of 16 or greater.

Results: Patients who recovered through antidepressant medication showed greater cognitive reactivity following the mood provocation than those who received cognitive behavior therapy. Regardless of type of prior treatment, the magnitude of mood-linked cognitive reactivity was a significant predictor of relapse over the subsequent 18 months. Patients whose mood-linked endorsement of dysfunctional attitudes increased by a minimum of 8 points had a significantly shorter time to relapse than those whose scores were not as elevated.

Conclusions: The vulnerability of remitted depressed patients for illness relapse may be related to the (re)activation of depressive thinking styles triggered by temporary dysphoric states. This is the first study to link such differences to prognosis following successful treatment for depression. Further understanding of factors predisposing to relapse/recurrence in recovered patients may help to shorten the potentially lifelong course of depression.

PubMed Disclaimer

Comment in

Similar articles

Cited by

Publication types

MeSH terms

Substances