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Mindfulness-Based Cognitive Therapy Effect on Depression and C-Reactive Protein Levels After 8 Weeks of Treatment

Mindfulness-Based Cognitive Therapy Depression Efficacy and Effects on Inflammatory Biomarker Levels

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02385786
Enrollment
43
Registered
2015-03-11
Start date
2011-11-30
Completion date
2012-08-31
Last updated
2022-03-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depressive Disorder

Keywords

mindfulness-based cognitive therapy, depression, treatment, mindfulness meditation, psychotherapy

Brief summary

This study will investigate the efficacy of an 8-week course in Mindfulness-Based Cognitive Therapy (MBCT) for adults with major depressive disorder (MDD) by ;measuring change from baseline to completion of treatment at 8 weeks in terms of depression severity using the Hamilton Depression Ratings Scale. We will measure change in C-Reactive Protein, a measure of inflammation, over the same time period.

Detailed description

This study will investigate the effectiveness of MBCT as a primary treatment for MDD. Twelve unmedicated subjects with MDD were enrolled in the study. All subjects with MDD underwent depression severity assessment at baseline and after the 8-week intervention was complete to measure change. In addition, the subjects underwent blood sampling at the same time points to measure C-Reactive Protein change over the 8 weeks. The primary goal of this pilot study is to determine the efficacy of MBCT as a primary treatment for adults with MDD. We will also measure change in the inflammatory biomarker C-Reactive Protein for an examination of the effects of depression treatment on this measure.

Interventions

BEHAVIORALMindfulness-Based Cognitive Therapy

Eight week course in mindfulness meditation training with elements of cognitive behavioral therapy

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* English speaking * Able to give informed consent * DSM-IV (SCID) Diagnosis of Major Depression * HAM-D17 score ≥ 17 * Good general medical health; no active significant uncontrolled medical illness * Free of antidepressant medication for a minimum of 6 weeks before study entry * Not needle phobic by self report

Exclusion criteria

* Axis I and II disorders including: Bipolar, Obsessive Compulsive Disorder, Psychosis, or Antisocial or Borderline Personality Disorder with suicidal risk * Major Depression with Psychotic Features * Actively suicidal * Recent (6 month) history of substance or alcohol dependence (DSM-IV criteria) * Meditation practice once or more per week * Yoga practice more than twice per week at study entry * Mini Mental Status Exam score \< 25or history of neurologic illness

Design outcomes

Primary

MeasureTime frameDescription
Hamilton Depression Rating Scale Change with MBCT treatmentWeek 0, 817-item clinician-rated measure of depression severity.

Secondary

MeasureTime frameDescription
C-Reactive Protein (Blood) Change with MBCT treatmentWeek 0-8An inflammatory biomarker that varies with levels of inflammation in the body

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026