Addressing Emotional and Cognitive Factors in Behavioral Weight Loss Treatment

National Institutes of Health (NIH)

Status

Completed

Conditions

Overweight

Obesity

Treatments

Behavioral: Affective and Cognitive Skills Training

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT00533052

K23 DK73536 (completed)

K23DK073536 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Behavioral weight loss, the current treatment of choice for moderate obesity, achieves impressive short term results, however, weight regain following treatment is a major problem. Over 50% of participants in behavioral weight loss programs report difficulty with internal antecedents to unhealthy weight control behaviors and this difficulty is associated with weight regain following treatment. Current treatment approaches do not adequately address these antecedents. The aim of this series of studies is to develop, implement, and evaluate a behavioral weight loss program modified to provide participants with skills to deal effectively with affective and cognitive difficulties. The study targets men and women with BMI of 27-40 who self-report difficulty with emotional and/or cognitive antecedents to unhealthy weight control behaviors. The study is an uncontrolled pilot study in 20 participants to initially assess acceptability and efficacy of the innovative treatment. The long-term goal of this research is to improve the weight loss maintenance outcomes of behavioral weight loss programs by addressing affective and cognitive antecedents to unhealthy weight control behaviors.

Enrollment

21 patients

Sex

All

Ages

21 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age between 21 and 70 years
Body mass index between 27 and 40
Score 5 or above on the internal disinhibition scale of the Eating Inventory

Exclusion criteria

Are currently participating in a weight loss program and/or are taking a weight loss medication or lost greater than or equal to 5% of body weight during the past six months
Are pregnant, lactating, less than 6 months postpartum or plan to become pregnant during the time frame of the investigation
Report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire (PAR-Q). Individuals endorsing joint problems, prescription medication usage, or other medical conditions that could limit exercise will be required to obtain written physician consent to participate.