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Pre-therapeutic Validation of the Virtual Reality-based Exposure Scenario for CBT "ReVBED" for the Induction of Food Craving in Patients With Bulimia and Binge Eating Disorder (BED) (RevBED)

C

Centre Hospitalier Universitaire de Saint Etienne

Status

Completed

Conditions

Binge-Eating Disorder
Bulimia Nervosa

Treatments

Behavioral: experimentation of the virtual reality "RevBED"

Study type

Interventional

Funder types

Other

Identifiers

NCT05385653
ANSM (Other Identifier)
21CH086

Details and patient eligibility

About

Food craving is a major therapeutic issue in Eating Disorders with binge eating: the Bulimia Nervosa and the Binge Eating Disorder (BED). Food craving is linked to compulsive eating and its apprehension is currently based on classic Cognitive and Behavioural Therapies (CBT). However, it remains difficult to induce in therapy and a significant number of patients do not respond to classic CBTs. The development of exposure scenarios for CBT in virtual reality (VR) has allowed a gain in efficacy and in particular therapeutic effects lasting longer after treatment. Nevertheless, the stimuli used are often simple food visuals and insufficiently consider the many factors influencing food craving (physical, psychological, socio-environmental...) and VR immersion is still limited by the use of 3D laptops (fixed) rather than wireless headsets.

Full description

Eating Disorders-specialized clinicians from Saint-Etienne University Hospital Center (CHU) and VR-specialized engineers from National School of Engineering of Saint-Etienne (ENISE) therefore collaborated in the creation of ReVBED, a VR-based exposure scenario for CBT for the induction of food craving in eating disorders with binge eating. ReVBED offers successive exposures to multimodal stimuli in a coherent scenario and in an immersive virtual environment via a wireless VR headset.

Our first objective is to validate the effectiveness of our scenario in inducing food craving in patients with bulimia and BED.

Enrollment

60 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients: who meet Diagnostic and Statistical Manual of Mental Disorders (DSM)-5 criteria for Bulimia Nervosa or Binge Eating Disorder
  • Controls: paired to patients on age and level of education

Exclusion criteria

  • Patients and controls:
  • Under legal protection measure (guardianship, curatorship or safeguard of justice)
  • Having a treatment being established and / or not stabilized (declarative) able to alter the physiological data recorded and the answers to the self-questionnaires
  • Having one or more sensory deficit(s) or disorder(s) incompatible with the use of VR equipment (declarative)
  • Patients: who have already benefited from specific care targeting food craving (declarative) Controls: with a score greater than or equal to 88 on the Bulimia Test (BULIT)

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

patients with bulimia or binge eating disorder
Experimental group
Description:
patients with bulimia or binge eating disorder
Treatment:
Behavioral: experimentation of the virtual reality "RevBED"
control
Other group
Description:
paired healthy controls
Treatment:
Behavioral: experimentation of the virtual reality "RevBED"

Trial contacts and locations

1

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Central trial contact

Aurélia GAY, MD; Hélène RAINGARD, CRA

Data sourced from clinicaltrials.gov

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