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Craving and Lifestyle Management Through Mindfulness Pilot Study

Craving and Lifestyle Management Through Mindfulness Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00643344
Acronym
CALMM
Enrollment
15
Registered
2008-03-26
Start date
2008-01-31
Completion date
2008-12-31
Last updated
2014-10-28

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

Conditions

Obesity

Keywords

obesity, mindfulness based stress reduction, diet and exercise, mindful eating, stress

Brief summary

The purpose of this study is to determine whether an innovative program that combines mindfulness-based stress reduction and mindful eating practices with diet and exercise guidelines (CALMM+ intervention) will lead to greater weight loss and more favorable body fat distribution than a conventional weight-loss program(Diet-Ex intervention).

Detailed description

Obesity is an important growing epidemic, with about 65% of Americans overweight (Flegal, Carroll et al. 2002). Psychological stress is widely cited anecdotally as a factor that causes people to engage in overeating, and studies provide strong evidence that stress can promote obesity. Stress induces selective preference of sweet, high-fat food and increases visceral fat depots. Chronic stress has also been shown to impair immune responses, including decreasing immune responses to vaccination. The proposed study will pilot test an innovative program that combines stress reduction and mindful eating practices with diet and exercise, Craving and Lifestyle Management through Mindfulness (CALMM+). This program will be compared with diet and exercise intervention alone (Diet-Ex). Approximately 20 persons will be randomized to the two groups, which will meet weekly for 16 weeks. Key outcome measures are weight, fat distribution (as measured by waist/hip ratio), perceived stress, and mood. These measures will be assessed in visits performed at baseline, 3 months, and 6 months. Data from this study are intended to provide pilot data for use in planning a larger randomized, controlled trial that will compare the effects of the CALMM+ and Diet-Ex interventions on the metabolic and psychological processes assessed in this pilot study.

Interventions

BEHAVIORALCraving and Lifestyle Management through Mindfulness(CALMM+)

MBSR is a program that provides systematic training in mindfulness meditation and gentle yoga as a self-regulation approach to reduce stress and improve medical and psychological symptoms. In this randomized controlled pilot study, we aim to test a 16-week intervention that further integrates diet and exercise into the CALMM program (CALMM+). This novel program, which includes elements drawn from MBSR, will be actively compared with the conventional diet and exercise group(TLC). Both groups will receive about 7 hours of in-class and out-of-class activities per week. The activities includes exercise, keeping dietary records, and stress reduction practices (if they are assigned to the intervention group).

Sponsors

National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
Mount Zion Health Fund
CollaboratorOTHER
Robert Deidrick Fund
CollaboratorUNKNOWN
University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy female * aged 18-50 * BMI range 25-45 * negative urine glucose test * must be able to provide informed consent

Exclusion criteria

* male * age less than 18 or menopausal * clinical diagnosis of eating disorder, diabetes, polycystic ovary syndrome, and coronary artery disease * history of anginal chest pain without adequate evaluation * substance abuse, mental health or medical condition that might interfere with study participation * use of medications containing corticosteroids * breastfeeding * non- English speaker * pregnant or planning to get pregnant in the next 6 months * previous Mindfulness Based Stress Reduction training * initiation of new class of psychiatric medications in past 2 months * currently on a weight loss diet

Design outcomes

Primary

MeasureTime frame
weightbaseline, 3 month, and 6 month assessments

Secondary

MeasureTime frame
fat distributionbaseline, 3 month, and 6 month assessments
perceived stressbaseline, 3 month, and 6 month assessments
moodbaseline, 3 month, and 6 month assessments

Countries

United States

Outcome results

None listed

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