Obesity, Overweight
Conditions
Keywords
Behavioral weight loss
Brief summary
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.
Interventions
BEHAVIORALAffective and Cognitive Skills Training
24-week, weekly, group behavioral weight loss treatment with affective and cognitive skills training
Sponsors
The Miriam Hospital
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
21 Years to 70 Years
Healthy volunteers
No
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body Mass Index | 6 months |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Attendance data | 6 months | — |
| Internal disinhibition as measured by the Eating Inventory | 6 months | The internal disinhibition subscale of the Eating Inventory ranges from 0 to 8, with high values indicating more disinhibition. |
| Treatment acceptability based on qualitative feedback | 6 months | — |
Countries
United States
Outcome results
None listed