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Efficacy of a Mindfulness Meditation Program for Social Anxiety Disorder

Efficacy of an Enhanced Mindfulness-based Intervention for Social Anxiety Disorder: A Pilot Feasibility Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01914874
Enrollment
39
Registered
2013-08-02
Start date
2013-07-31
Completion date
2015-01-31
Last updated
2015-07-01

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

Conditions

Social Anxiety Disorder

Keywords

Community Sample

Brief summary

The aim of this study is to evaluate the feasibility and initial efficacy of an enhanced mindfulness-based program that includes mindful exposure to reduce anxiety and avoidance of social situations, and the Buddhist practice of self-compassion aimed at reducing harsh judgment and self-criticism that is characteristic of people with social anxiety disorder.

Detailed description

The purpose of this pilot study is to evaluate the feasibility and initial efficacy of an enhanced mindfulness-based intervention for SAD (MIND-SAD) that incorporates the following components: training in classical mindfulness, including concentration and insight (vipassana) meditation; training in self-compassion; and mindful exposure. An exploratory aim of the study is to evaluate the effects of the mindfulness intervention on biological markers of stress reactivity, including salivary cortisoland salivary alpha-amylase. The study is a two-arm, parallel design, prospective study comparing 12 weekly sessions of MIND-SAD delivered in a group format versus a wait-list control (WLC).

Interventions

BEHAVIORALMindfulness Meditation

Sponsors

Hopital Montfort
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Primary diagnosis of Social Anxiety Disorder; Baseline score of 30 or higher on the Liebowitz Social Anxiety Scale; Baseline score of 4 or higher on the Clinical Global Impression of Severity

Exclusion criteria

* Lifetime history of psychosis or bipolar disorder; substance abuse in the past 12 months; diagnosis of borderline or antisocial personality disorder; serious suicide risk; currently in psychotherapy; regular meditation or yoga practice in the past 12 months

Design outcomes

Primary

MeasureTime frame
Social Phobia Inventorychange from baseline at weeks 6, 12 and 3 months follow-up
Clinician-rated Liebowitz Social Phobia Scalechange from baseline at weeks 6, 12 and 3 months follow-up

Secondary

MeasureTime frame
Social Adjustment Scale-Self-Reportchange from baseline at weeks 6 and 12 and 3 months follow-up
CGI-Severity of Illnesschange from baseline at weeks 6, 12 and 3 months follow-up
Beck Depression Inventorychange from baseline at weeks 6, 12 and 3 months follow-up
Self-Compassion Scalechange from baseline at weeks 6, 12 and 3-months follow-up
Five Facet Mindfulness Questionnairechange from baseline at weeks 6, 12 and 3 months follow-up

Other

MeasureTime frame
Salivary cortisolchange from baseline at week 12
Study compliance: attendance and homeworkcompliance will be assessed at each week during the 12-week mndfulness meditation program
Salivary alpha-amylasechange from baseline at week 12

Countries

Canada

Outcome results

None listed

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