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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02717247
Other study ID # 2015-A00028-41
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date February 2016
Est. completion date May 2, 2019

Study information

Verified date January 2020
Source Hôpital le Vinatier
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Obesity is worldwide a public health problem. According to World Health Organization (WHO), overweight and obesity are the fifth death risk factor worldwide. At least 2.8 million adults die each year. Food addiction is one of the causes of obesity that may benefit from new therapeutic options.


Description:

Transcranial random noise stimulation is a noninvasive brain stimulation technic. The modulation of the electrical activity of the right and left dorsolateral prefrontal cortex (DLPFC) by tRNS is able to act on the phenomenon of craving in other addictions. This allows us to make the assumption that tRNS stimulation could constitute a treatment for food addiction especially in obesity.


Recruitment information / eligibility

Status Terminated
Enrollment 13
Est. completion date May 2, 2019
Est. primary completion date April 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Female or male between 18 and 65 years old

- Patients suffering from obesity, with a BMI = 30.

- Food dependence score at the Yale Food addiction Scale = 3

Exclusion Criteria:

- Presence of a an other psychiatric diagnosis of Axis I (DSM IV);

- Presence of addictive comorbidity other than food addiction

- Psychotropic treatment;

- Pregnancy or lactation;

- Contraindication to fMRI .

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Active tRNS
The intervention consists in active tRNS stimulation with cathode above the left dorsolateral prefrontal cortex (DLPFC) which corresponds to the F3 location given by the 10-20 system. Anode is above the right dorsolateral prefrontal cortex (F4). 100Hz-650Hz, 2mA, 30min, twice daily, 5 days
Sham tRNS
The intervention consists in placebo or sham tRNS stimulation electrode are above F3 and F4. Voltage will be ramped at the begin and end of a stimulation for 30 seconds. Placebo stimulation will consist of just applying the ramps at the begin and end of the stimulation.

Locations

Country Name City State
France Centre Hospitalier Le Vinatier Bron Cedex

Sponsors (1)

Lead Sponsor Collaborator
Hôpital le Vinatier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Effects on craving frequencies by questionnaires scores and declarative number of food Change from baseline after 3 months
Secondary change in body weight Change from baseline after 3 months
Secondary change in waist circumference Change from baseline after 3 months
Secondary change in body mass index Change from baseline after 3 months
Secondary change in biological markers such as lipid profile, ghrelin, leptin, prolactin Change from baseline after 3 months
See also
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