Transcranial Magnetic Stimulation, Embodied Cognition and Bulimic Craving
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 30
- Locations
- 2
- Primary Endpoint
- Motor response time
Study Overview
Brief Summary
Bulimic patients suffering from binge eating or "craving" a pressing need to eat, with a sense of unease and anxiety, relieved by food intake. The phenomenon of craving bulimia may be considered appropriately by using paradigms developed in the framework of embodied cognition theories.
In bulimic, a study with 20 bulimic patients proved an automatic attraction (unconscious) for food in these patients, as measured by reaction time.
Moreover, a therapeutic explored in bulimia (particularly on reducing craving), is repeated transcranial magnetic stimulation (rTMS). Studies have shown that a single session of rTMS to the dorsolateral prefrontal cortex left (DLPFC) reduces significantly the food craving among bulimics, 24 hours after stimulation. But the therapeutic efficacy of TMS on bulimia to more than 24 hours has not yet been demonstrated, and the psycho-cognitive underlying mechanisms have not yet been explored.
Detailed Description
The exams / treatments of the study include:
- a 20 minute session of rTMS at a frequency of 10 Hz.
- cognitive testing and attention, which will be made on the computer before and 24 hours after the session of rTMS.
Cognitive test consist in , on a computer screen:
- Is first displayed, food and non-food words. The patient must pull a lever to it if the letter A is present in the word and push the lever if the letter A is missing the word.
- Then presents a series of food and non-food words. The patient must pull a lever to it if it deems that the word has a positive meaning and push the lever if it determines that the word has a negative meaning
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Masking
- Single (Participant)
Eligibility Criteria
- Ages
- 18 Years to 40 Years (Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •right-handed patient
- •Patients without psychotropic treatment or treatment with a stable and unchanged for over a month.
- •Normal BMI
Exclusion Criteria
- •Previous history of seizures or epilepsy.
- •Participants with a somatic problem restricted movement or an uncorrected visual acuity problem.
- •History of head trauma, neurological disease or unstabilized serious physical illness.
- •Major Depressive Episode at the time of the study
Outcomes
Primary Outcomes
Motor response time
Time Frame: 24h after rTMS session
time taken to pull or push the lever in cognitive tests (composite measure)
Secondary Outcomes
No secondary outcomes reported