Boulimia nervosa and Binge eating disorder
Conditions
Interventions
Participants are randomly divided into three groups. The first (experimental)
group will be receiving a treatment with behavioral regulation-IIs focused
directly on the binge itself. The second (exp
they
only form goal intentions. In each group there are three individual weekly
treatment sessions, during three weeks.
Sponsors
Universiteit Maastricht
Eligibility
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: - Boulimia Nervosa or Binge Eating Disorder diagnosed according to the DSM-V criteria. - age: 18 years or older
Exclusion criteria
Exclusion criteria: - Anorexia Nervosa diagnosed according to the DSM-V criteria. - BMI
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The ultimate goal is to reduce the number of binges. This is measured by (1) the foodintake diary, which specifically requests binge eating, (2) the Eating Disorder Examination Questionnaire (EDE-Q; Fairburn & Beglin, 1994) and (3) the Eating Disorder Inventory-II (EDI II ; Garner & Van Strien, 2002). | — |
Secondary
| Measure | Time frame |
|---|---|
| A secundary study parameter is negative affect. This will be measured by the Positive and Negative Affect Schedule (PANAS; Watson, Clark & Tellegen, 1988). | — |
Countries
Netherlands
Outcome results
None listed