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Treating Subthreshold Depression in Primary Care: A Randomized Controlled Trial of Behavioral Activation With Mindfulness.

Annals of family medicine
March 1, 2018
Samuel Y S Wong et al. (11 authors)
Journal ArticleMulticenter StudyRandomized Controlled TrialResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to assess the efficacy of group-based behavioral activation with mindfulness (BAM) for treating subthreshold depression in primary care patients.

Results Summary

BAM patients showed a slightly more favorable change in depressive symptoms compared to usual care, with a statistically significant but modest effect size (Cohen’s d=0.35). The intervention also reduced the incidence of major depressive disorder at 12 months.

Population

Adult patients aged 18+ with subthreshold depression in Hong Kong primary care clinics.

Effective Dosage

Eight 2-hour weekly BAM sessions.

Duration

8 weeks (intervention), with follow-up at 12 months.

Interactions

None mentioned

Extracted Claims (2)
InterventionDirectionEndpointPopulationDosageImpactClaim #
group-based behavioral activation with mindfulness (BAM)
decrease
depressive symptoms on the Beck Depression Inventory-II
patients with subthreshold depression in primary care
between-group mean difference in score = -3.85; 95% CI, -6.36 to -1.34; Cohen d = 0.45
had a slightly more favorable change in levels of
#1
group-based behavioral activation with mindfulness (BAM)
decrease
major depression
patients with subthreshold depression in primary care
-
reducing the incidence of
#2
Abstract

PURPOSE: We undertook a randomized controlled trial to assess the efficacy of group-based behavioral activation with mindfulness (BAM) for treating subthreshold depression in primary care in Hong Kong. METHODS: We recruited adult patients aged 18 years or older with subthreshold depression from public primary care clinics and randomly assigned them to a BAM intervention group or a usual care group. The BAM group was provided with eight 2-hour weekly BAM sessions by trained allied health care workers. Patients in the usual care group received usual medical care with no additional psychological interventions. The primary outcome was depressive symptoms measured by the Beck Depression Inventory-II at 12 months. Secondary outcomes included incidence of major depressive disorder at 12 months. We assessed quality of life, activity and circumstances change, functional impairment, and anxiety at baseline, end of intervention, 5 months, and 12 months. RESULTS: We randomly allocated 115 patients to the BAM intervention and 116 patients to usual care. At 12 months, compared with usual care peers, BAM patients had a slightly more favorable change in levels of depressive symptoms on the Beck Depression Inventory-II (between-group mean difference in score = -3.85; 95% CI, -6.36 to -1.34; Cohen CONCLUSIONS: Group BAM appears to be efficacious for decreasing depressive symptoms and reducing the incidence of major depression among patients with subthreshold depression in primary care, although generalizability of our findings may be limited.

Medical Subject Headings (MeSH)
AdultAgedCost-Benefit AnalysisDepressionDepressive Disorder, MajorFemaleHong KongHumansLogistic ModelsMaleMiddle AgedMindfulnessPrimary Health CarePsychiatric Status Rating ScalesQuality of Life
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality85/10
Citation Metrics
Total Citations23
Citations/Year3.3
Relative Citation Ratio1.61
NIH Percentile67.5%
Research Impact Scores
APT Score0.50
Weight Score2.23
Normalized Score0.67
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