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A Preliminary Study: Efficacy of Mindfulness-Based Cognitive Therapy versus Sertraline as First-line Treatments for Major Depressive Disorder.

Stuart J. Eisendrath, Erin P Gillung, Kevin L. Delucchi, Daniel H. Mathalon, Tony T. Yang, Derek D Satre, Rebecca Rosser, Walter E B Sipe, Owen M Wolkowitz

Mindfulness June 1, 2015 DOI: 10.1007/s12671-014-0280-8 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Open-label, nonrandomized controlled trial (pilot study) Peer reviewed
Sample size 43
Population Patients with acute major depressive disorder
Interventions Mindfulness-Based Cognitive Therapy (MBCT) sertraline
Duration 8 weeks
Measures 17-item clinician-rated Hamilton Depression Severity Rating Scale (HAMD-17), 16-item Quick Inventory of Depressive Symptomatology-Self-Report (QIDS-SR16)
Topics Depression Meditation
Keywords Antidepressants Cognitive therapy Sertraline
Key findings Both MBCT and sertraline monotherapy produced significant improvement in depression over 8 weeks, with no difference between groups on the clinician-rated HAMD-17. The MBCT group showed greater improvement on the self-rated QIDS-SR16, which the authors suggest may reflect additional subjective benefit from enhanced self-efficacy skills.

Abstract

Major depressive disorder (MDD) is the leading cause of disability in the developed world, yet broadly effective treatments remain elusive. The primary aim of this pilot study was to investigate the efficacy of Mindfulness-Based Cognitive Therapy (MBCT) monotherapy, compared to sertraline monotherapy, for patients with acute MDD. This open-label, nonrandomized controlled trial examined a MBCT cohort (N=23) recruited to match the gender, age, and depression severity of a depressed control group (N=20) that completed 8 weeks of monotherapy with the antidepressant sertraline. The 17-item clinician-rated Hamilton Depression Severity Rating Scale (HAMD-17) was the primary outcome measure of depression to assess overall change after 8 weeks and rates of response and remission. The 16-item Quick Inventory of Depressive Symptomatology-Self-Report (QIDS-SR16) was the secondary outcome measure to further assess depression severity. Both cohorts were demographically similar and showed significant improvement in depression ratings. No difference was found in the degree of change in HAMD-17 scores (t(34) = 1.42, p = .165) between groups. Secondary analysis showed statistically significant differences in mean scores of the QIDS-SR16 (t (32) = 4.39, p < 0.0001), with the MCBT group showing greater mean improvement. This study was limited by the small sample size and non-randomized, non-blinded design. Preliminary findings suggest that an 8-week course of MBCT monotherapy may be effective in treating MDD and a viable alternative to antidepressant medication. Greater changes in the self-rated QIDS-SR16 for the MBCT cohort raise the possibility that patients derive additional subjective benefit from enhanced self-efficacy skills.

Comparable studies

Other non-randomized and open-label trials on depression, most cited first.

Study Year Design Participants
Psilocybin with psychological support for treatment-resistant depression: an open-label feasibility study. Patients with moderate-to-severe, unipolar, treatment-resistant major depression 2016 Open-label feasibility trial n = 12
Psilocybin with psychological support for treatment-resistant depression: six-month follow-up. Patients with severe, unipolar, treatment-resistant major depression 2017 Open-label trial n = 20
Quality of Acute Psychedelic Experience Predicts Therapeutic Efficacy of Psilocybin for Treatment-Resistant Depression Patients with treatment-resistant depression 2018 Clinical trial n = 20
Rapid Resolution of Suicidal Ideation After a Single Infusion of anN-Methyl-D-Aspartate Antagonist in Patients With Treatment-Resistant Major Depressive Disorder Subjects with DSM-IV-diagnosed treatment-resistant major depressive disorder 2010 Open-label trial n = 33
Antidepressant Effects of a Single Dose of Ayahuasca in Patients With Recurrent Depression Patients with recurrent depression 2015 Open-label trial n = 17

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