The primary objective of the current study is to investigate whether self-disgust is heightened in patients with AN. If this indeed is the case, this would provide important leads to improve existing treatment options for AN.
ID
Source
Brief title
Condition
- Eating disorders and disturbances
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
By briefly (i.e., 4 x 10 seconds) exposing individuals with and without AN
toward a personalized avatar in Virtual Reality (VR) with overweight, we will
determine in real-time whether indeed self-disgust is characteristic of AN.
Facial electromyography (fEMG) will be used to assess psychophysiological
disgust responses with the levator labii as the classic index of disgust.
Self-reported state levels of disgust will be assessed with visual analogue
scales.
Secondary outcome
• Fear of food intake indexed with the Anxiety about eating subscale of the
Fear of Food Measure
• Food intake expectancy indexed with the Weight gain estimation task
Background summary
Investigating specific factors contributing to the development and maintenance
of anorexia nervosa (AN) is important to inform treatment options, especially
because relapse rates are high in this population. So far, prior interventions
targeting food restriction in AN have focused on the reduction of fear of food
intake. We recently developed a theoretical model incorporating key mechanisms
of existing theories and described how body-related self-disgust can play a
central role in the onset and maintenance of AN. Because treatments currently
do not specifically address self-disgust, this could explain why their
effectiveness is often limited on the long term: residual levels of
self-disgust after treatment could make individuals vulnerable to relapse. To
effectively reduce disgust, habituation via prolonged exposure is considered
critical to weaken the intrinsically revolting nature of disgust-eliciting
objects. However, it is only justifiable to start testing such a new
interventional approach, after the validity of the underlying theoretical model
has been thoroughly investigated.
Study objective
The primary objective of the current study is to investigate whether
self-disgust is heightened in patients with AN. If this indeed is the case,
this would provide important leads to improve existing treatment options for
AN.
Study design
This study will use an observational design (case-control study).
Study burden and risks
In this observational study participants will be asked to fill out seven
questionnaires, engage in a VR free-viewing task during which fEMG responses
are being recorded, and perform two computer tasks. In total, the time
investment will be approximately 105 minutes. The study might elicit negative
affect in the short term in the patient group, due to the brief presentation of
eating disorder relevant stimuli. Because all patients will be in treatment at
the time of the study, any negative effects of the study can be discussed with
their therapists. Since individuals with heightened levels of eating disorder
symptoms are excluded from participation in the comparison group and on basis
of positive experiences with prior studies in which we included adolescent
girls in a comparison group for a study regarding disgust and eating disorder
symptoms, we do not expect that the current study will have any negative effect
on participants in the comparison group, and if so, we expect this to be only
temporary. The study is expected to advance our understanding of the
persistence of food restriction in individuals with AN. Although several
studies so far have linked disgust to AN, it remains entirely unclear what
exactly elicits disgust in individuals with AN. By studying disgust responses
in real-time, the current study will help to get insight into the exact nature
of disgust in AN which will help to determine what might be important targets
for treatment.
Nieuwe Stationsweg 15
Haren 9751 SZ
NL
Nieuwe Stationsweg 15
Haren 9751 SZ
NL
Listed location countries
Age
Inclusion criteria
Inclusion criteria for the patient group:
• In treatment at the Department of Eating Disorders of Accare
• Having a current formal diagnosis of anorexia nervosa according to DSM-5
criteria
• Aged 12 to 19 years old
• Female gender
• Being cognitively able to take part in the study, as judged by their therapist
Inclusion criteria for the comparison group:
• Aged 12 to 19 years old
• Female gender
• Having a healthy weight. The TNO (2010) BMI for age growth curve will be used
to determine an age adjusted BMI range which corresponds with adult BMI
classifications for a healthy weight (i.e., BMI between 18,5 and 24,9).
Exclusion criteria
A potential participant who meets any of the following criteria will be
excluded from participation in this study:
• Aged > 19 years
• Aged < 12 years
• Not being able to speak and read Dutch
• Not being able to do the experiment without glasses
Additional exclusion criteria for the patient group:
• Being medically unstable and/or admitted to the hospital
• Being in an acute crisis (e.g., due to suicidality or substance abuse)
Additional exclusion criteria for the comparison group:
• Having heightened levels of eating disorder symptoms (EDE-Q >= 4; Mond, Hay,
Rogers & Owen, 2006).
• Being underweight (age adjusted BMI below norms for a healthy weight) or
overweight (age adjusted BMI above norms for a healthy weight).
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL84582.042.23 |