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Feasibility study of mindfulness-based cognitive therapy for anxiety disorders in a Japanese setting.

BMC research notes
January 1, 1970
Mitsuhiro Sado et al. (7 authors)
Clinical TrialJournal ArticleHuman StudyClinical
Study Details

Study Goal

The researchers aimed to evaluate the effectiveness of Mindfulness-Based Cognitive Therapy (MBCT) for anxiety disorders in a context of high pharmacotherapy rates.

Results Summary

The study found statistically significant improvements in both state and trait anxiety (measured by STAI) from early stages of the intervention, with additional improvements in some secondary outcomes.

Population

Patients aged 20-74 with any diagnosis of anxiety disorders (71.4% female, mean age 45.0).

Effective Dosage

8 weekly 2-hour sessions followed by 2 monthly booster sessions.

Duration

8 weeks (plus 2 monthly boosters).

Interactions

None mentioned

Extracted Claims (3)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Mindfulness-based cognitive therapy (MBCT)
decrease
The State-Trait Anxiety Inventory (STAI)-state
patients with any diagnosis of anxiety disorders, between the ages of 20 and 74
-
showed statistically significant improvement
#1
Mindfulness-based cognitive therapy (MBCT)
decrease
The STAI-trait
patients with any diagnosis of anxiety disorders, between the ages of 20 and 74
-
showed improvement at a high significance level
#2
Mindfulness-based cognitive therapy (MBCT)
decrease
some other secondary outcomes
patients with any diagnosis of anxiety disorders, between the ages of 20 and 74
-
showed significant improvement
#3
Abstract

OBJECTIVE: Mindfulness-based cognitive therapy (MBCT) could be a treatment option for anxiety disorders. Although its effectiveness under conditions of low pharmacotherapy rates has been demonstrated, its effectiveness under condition of high pharmacotherapy rate is still unknown. The aim of the study was to evaluate effectiveness of MBCT under the context of high pharmacotherapy rates. RESULTS: A single arm with pre-post comparison design was adopted. Those who had any diagnosis of anxiety disorders, between the ages of 20 and 74, were included. Participants attended 8 weekly 2-hour-long sessions followed by 2 monthly boosters. Evaluation was conducted at baseline, in the middle, at end of the intervention, and at follow-up. The State-Trait Anxiety Inventory (STAI)-state was set as the primary outcome. Pre-post analyses with mixed-effect models repeated measures were conducted. Fourteen patients were involved. The mean age was 45.0, and 71.4% were female. The mean change in the STAI-state at every point showed statistically significant improvement. The STAI-trait also showed improvement at a high significance level from the very early stages. The participants showed significant improvement at least one point in some other secondary outcomes. Trial registration Retrospectively registered at the University Hospital Medical Information Network on 1st August 2013 (ID: UMIN000011347).

Medical Subject Headings (MeSH)
AdultAgedAnxietyAnxiety DisordersCognitive Behavioral TherapyFeasibility StudiesFemaleHumansMiddle AgedMindfulnessRetrospective StudiesTreatment OutcomeYoung Adult
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality60/10
Citation Metrics
Total Citations6
Citations/Year0.9
Relative Citation Ratio0.45
NIH Percentile24.5%
Research Impact Scores
APT Score0.50
Weight Score1.35
Normalized Score0.62
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