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Decision-making and Risk-taking in Bulimia

Identification of Decision Making Processes in Food, Risky and Steal Situations in Bulimia Nervosa

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04041024
Acronym
FaciB
Enrollment
59
Registered
2019-08-01
Start date
2020-10-28
Completion date
2021-06-15
Last updated
2021-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bulimia Nervosa

Keywords

computational psychiatry, decision making, risk, food, monetary, eating disorder

Brief summary

This trial is a set of four independent experiments involving for each of them functional and structural MRI data acquisition. They aim at investigating decision making mechanisms in bulimia nervosa when participants have to make food or monetary choices under specific conditions that mimic binge eating episodes or kleptomania which are two major symptoms of bulimia nervosa. All experiments are cross sectional studies. Each experiment is subdivided into two parts: a first part without any MRI data acquisition and during which all the tasks are performed. This part aims at making sure that a behavioral effect is observed before starting MRI data acquisition. The second part aims at investigating the neural correlates observed in the first part and additionally, at reproducing the behavioral effects observed in the first part. Therefore the first part may be regarded as an independent study as compared to the second part.

Detailed description

Each part of each experiment is built of a main task, a set of secondary tasks and questionnaires. Only the main task changes from one experiment to another. Within each experiment, the only difference between the two parts is that the main task is performed while participants are being scanned in an MRI scanner. Details of the tasks are provided below. Each part of each experiment is performed over one visit only and is a cross sectional study. The visit is dedicated to the tasks. Questionnaires may be filled during the visit or at participant's home within the week following the visit for questionnaires which are not assessing participant's state. Questionnaires assessing participant's state are filled during the visit at appropriate time. The total number of participants mentioned below is the sum of the planned number of participants within each group, i.e. patients and healthy participants, within each part of each experiment.

Interventions

OTHERtasks and questionnaires

Each of the 4 experiments is built of a main task. The first task involves a first phase of subjective valuation of food items. The second phase requires from the participant to make a choice between two out of three food items selected by the computer.

Sponsors

Hôpital le Vinatier
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* men and women aged 18 to 35 years with bulimia nervosa according to DSM 5 criteria for the patient's group * For the control group, men and women with the same age range being concerned by food intake and their body shape but without any history of eating disorder. * All participants must have signed an informed consent form and be affiliated to the French public health insurance. * for MRI scans, all participants must be right handed.

Exclusion criteria

* antisocial personality disorder, * borderline personality disorder * addiction to alcohol or psychoactive agent, ADHD, any psychotic disorder, * obesity of class 1 or 2 * istory of psychiatric disorder for the control group * history of neurological disorder for both groups * intermittent explosive disorder * any counter indication to MRI scans for the parts of experiments which take place in the MRI scanner.

Design outcomes

Primary

MeasureTime frameDescription
oxygen variation in the brain10 daysBrain activity related to task performance collected in the MRI scanner.Blood Oxygen Level Dependent response synchronized with any event of interest during the task. Events of interests are: * Onset time of any visual stimulus * Onset time of any response of the participant.

Secondary

MeasureTime frameDescription
Task related parameters10 daysreaction times computed as the duration in ms between the onset time of the stimulus and the onset time of the participant's answer. Several tasks may be involved in each experiment including in the MRI scan. These rules apply to all tasks.
Skin conductance response related to events in the task performed while the signal is being collected10 daysSkin conductance response in microSiemens synchronized with any event of interest during the task. Events of interests are: * Onset time of any visual stimulus * Onset time of any response of the participant
cardiac frequency in beats per minute related to events in the task performed while the signal is being collected10 dayscardiac frequency is computed from the pulse plethysmogram sensor signal while the participant is performing the task. Task during which this signal is collected may be one of the tasks performed in the scanner as well as tasks performed outside the scanner.
parameters of eye movements extracted from the eye tracking signal is being collected10 daysThe parameters computed are X and Y position of the eye by amplitude of variation of pupil size over a time window synchronized with events in the task
Eating Disorders Examination (EDE-Q)10 daysThe EDE is a semi-structured interview conducted by a trained clinician to assess the psychopathology associated with the diagnosis of an eating disorder. The EDE is rated through the use of four subscales (restraint, eating concern, weight concern, shape concern) and global score.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026