A randomized, controlled clinical trial: the effect of mindfulness-based cognitive therapy on generalized anxiety disorder among Chinese community patients: protocol for a randomized trial.
Study Goal
The researchers aimed to compare the clinical effectiveness of an eight-week Mindfulness-Based Cognitive Therapy (MBCT) program with a psycho-education program and usual care in reducing anxiety symptoms in individuals with generalized anxiety disorder.
Results Summary
The study proposed a randomized controlled trial to evaluate MBCT's effectiveness, with primary endpoints focusing on changes in anxiety and worry scores. Findings are expected to advance knowledge on managing generalized anxiety disorder and inform future research, but specific results are not yet reported in the abstract.
Population
Adults with generalized anxiety disorder recruited from community-based clinics, screened using the Structured Clinical Interview for DSM-IV (SCID).
Effective Dosage
Not specified (eight-week MBCT program, but exact session details not provided).
Duration
Eight weeks, with a 9-month post-treatment follow-up.
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
Mindfulness-Based Cognitive Therapy (MBCT) program | decrease | generalized anxiety disorders | - | - | may be effective in the treatment | #1 |
MBCT program plus usual care | decrease | anxiety symptoms | people suffering from generalized anxiety disorder | - | compare the clinical effectiveness | #2 |
psycho-education programme plus usual care | decrease | anxiety symptoms | people suffering from generalized anxiety disorder | - | compare the clinical effectiveness | #3 |
usual care | decrease | anxiety symptoms | people suffering from generalized anxiety disorder | - | compare the clinical effectiveness | #4 |
BACKGROUND: Research suggests that an eight-week Mindfulness-Based Cognitive Therapy (MBCT) program may be effective in the treatment of generalized anxiety disorders. Our objective is to compare the clinical effectiveness of the MBCT program with a psycho-education programme and usual care in reducing anxiety symptoms in people suffering from generalized anxiety disorder. METHODS: A three armed randomized, controlled clinical trial including 9-month post-treatment follow-up is proposed. Participants screened positive using the Structure Clinical Interview for DSM-IV (SCID) for general anxiety disorder will be recruited from community-based clinics. 228 participants will be randomly allocated to the MBCT program plus usual care, psycho-education program plus usual care or the usual care group. Validated Chinese version of instruments measuring anxiety and worry symptoms, depression, quality of life and health service utilization will be used. Our primary end point is the change of anxiety and worry score (Beck Anxiety Inventory and Penn State Worry Scale) from baseline to the end of intervention. For primary analyses, treatment outcomes will be assessed by ANCOVA, with change in anxiety score as the baseline variable, while the baseline anxiety score and other baseline characteristics that significantly differ between groups will serve as covariates. CONCLUSIONS: This is a first randomized controlled trial that compare the effectiveness of MBCT with an active control, findings will advance current knowledge in the management of GAD and the way that group intervention can be delivered and inform future research. Unique Trail Number (assigned by Centre for Clinical Trails, Clinical Trials registry, The Chinese University of Hong Kong): CUHK_CCT00267.