Obesity Clinical Trial
Official title:
Meditation-Based Treatment for Binge Eating Disorder
The purpose of this study is to assess the relative effectiveness of a mindfulness meditation-based intervention for binge eating disorder in comparison to a psycho-educational intervention and a waiting-list control group.
As many as 30% of individuals seeking treatment for obesity meet the Diagnostic and
Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) criteria for binge eating
disorder (BED). BED is marked by recurrent episodes of bingeing, accompanied by feelings of
loss of control, and involves chronic disregulation of physiological, emotional and
behavioral systems. Meditation-based interventions have been used successfully to treat
disorders with similar addictive and disregulatory characteristics, but have not been
applied to treating BED. Data from an uncontrolled pilot study suggests that such an
intervention can have marked immediate impact on decreasing episodes of binge eating and
other associated characteristics in obese women. Therefore, this study incorporates
appropriate comparison conditions to further investigate the efficacy of a mindfulness
meditation-based intervention as a treatment component for treating BED symptoms.
Exploratory aspects include further development of a manual, establishment of effect size
(in comparison to appropriate comparison groups), inclusion of a more diverse population,
and of measures that address: 1) individual differences in treatment response, 2) possible
mechanisms, 3) time course of response, and 3) impact on medical/health variables.
Women from two communities will be randomly assigned to 3 conditions: 1) an 8-week
manualized meditation-based group intervention, 2) a psychoeducational comparison condition,
or 3) a waiting-list control. Primary outcome variables will be changes in binge eating
behaviors, and associated measures of depression, anxiety, self-esteem, and diet; secondary
variables include medical variables sensitive to dietary change (i.e., weight; blood
pressure; lipid profile; blood glucose levels), and process variables related to meditation
practice, such as the Tellegen Absorption Scale, perceived value and use of the meditation
practice, and experiences of increased control and awareness. Participants will be evaluated
pre- and post-treatment, and at 1, 3, and 6 months followup. This data would then support
the further investigation of a meditation-based intervention as part of a more comprehensive
treatment program for BED.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment
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