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Effect of Self Regulation With Mindfulness Training on Body Mass Index and Cardiovascular Risk Markers in Obese Adults

Enhancing Self Regulation With Mindfulness Training and Its Effect on Body Mass Index and Cardiovascular Risk Markers in Obese Adults: A Randomized Pilot Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01375504
Enrollment
36
Registered
2011-06-17
Start date
2011-07-31
Completion date
2012-04-30
Last updated
2012-04-19

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

Conditions

Obesity

Keywords

Obesity, Body Mass Index, Mindfulness Training, Attention and Interpretation Therapy

Brief summary

This study is designed to assess the effect of a mindfulness training program with special focus on diet and nutrition vs. dietary counseling in 40 obese adults (BMI range 30-40) and their partner/spouses (irrespective of their BMI), in a 6-month pilot randomized controlled trial.

Detailed description

Obesity is associated with deficits in self regulation. Approaches that foster increased non-judgmental present moment awareness and increased acceptance have been demonstrated to enhance self regulation. One commonly used approach that synthesizes these concepts is mindfulness training. This study is designed to assess the effect of a mindfulness training program with special focus on diet and nutrition, on body mass index, cardiovascular risk markers, peripheral blood telomere length and telomerase levels in obese adults. The mindfulness training program is adapted from the Attention and Interpretation Therapy developed by study investigators at Mayo Clinic. The study is designed as a 6-month pilot randomized controlled trial involving 40 obese adults and their partners/spouses with standard dietary counseling as the control intervention. Promising feasibility and efficacy data from the study will prompt us to pursue a larger, multi-center trial to more definitively test this program as well as apply this intervention in clinical practice.

Interventions

BEHAVIORALDietary Counseling

The control group will receive two sessions of dietary counseling (with instruction to follow a weight loss program) provided by a clinical dietician, consistent with current routine care for adults with obesity.

The mindfulness program will be administered over three 90-minute sessions by a physician and clinical dietician with expertise in mind-body medicine and nutrition.

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

PRIMARY PARTICIPANT Inclusion Criteria: * Obese adults (BMI ≥ 30) * Currently working at Mayo Clinic Rochester * Able to provide informed consent * Stable weight (within + 10 pounds) during the three months prior to enrolling in the study

Exclusion criteria

* Currently (in the past six months) attending a weight loss program * Underlying genetic or endocrine cause for weight gain * Current cancer * Medications known to affect weight (corticosteroids, antidepressants, anti psychotics, mood stabilizers, and anti-epileptic medications) * Musculoskeletal conditions affecting the ability to adequately perform general physical activity * Active smoking * Substance abuse * Quitting smoking within 6 months of enrolling in the study * Have clinically significant acute unstable neurological, psychiatric, hepatic, renal, cardiovascular or respiratory disease that will prevent participation in the study * Have an established practice of meditation for three or more months * Not willing to complete study outcome measures. PARTNER/SPOUSE Inclusion Criteria: * Able to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline to a healthier lifestyle.6 MonthsImprovement in general health.

Secondary

MeasureTime frameDescription
Change from baseline in vital signs.6 MonthsBody mass index (BMI) and absolute and percentage weight loss will be compared.
Change from baseline in laboratory values.6 MonthsPeripheral blood telomere length and telomerase levels, and cardiovascular risk markers will be compared.
Change from baseline in stress management.6 MonthsStress, anxiety, and quality of life will be measured on various study questionnaires.
Change in baseline on different aspects of eating.6 MonthsMindful eating, self efficacy and self regulation in eating will be compared.

Countries

United States

Outcome results

None listed

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