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The Effect of Brain Stimulation (tDCS) in Food Cravings Control in Overweight/Obese Women

Primary Purpose

Obesity

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
tDCS
Sham brain stimulation
Go-No GO task
Sponsored by
University of California, Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring food cravings, neuromodulation, brain, cognitive control, tDCS, prefrontal cortex, MRI, food addiction

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

BMI between 28 and 40 kg/m2 high scores in the Yale-Food Addiction-Scale right-handed

Exclusion Criteria:

  • History of anorexia nervosa or bulimia or binge eating disorder
  • Any contraindication to undergo MRI
  • Use of psychotropic medications and/or opiate pain medications.
  • Current or past alcohol or drug abuse problem or smoking
  • Pregnancy
  • Current use of weight loss medication or currently participating in a weight loss program.
  • History of seizures, epilepsy or factors/medications associated with lowered seizure threshold.
  • History of brain disease or major neurological disorder or mental disorder
  • History of brain surgery or history of loss of consciousness >15 min
  • History of major gastrointestinal surgery including weight loss surgery
  • History of endocrine imbalances including diabetes, thyroid disease, Cushing's disease, metabolic syndrome and polycystic ovary.

Sites / Locations

  • University of California

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

tDCS and Go-No Go task

Sham brain stimulation and Go-No Go task

Arm Description

Certain randomly assigned participants will receive tDCS to the DLPFC for 8 daily 20-minute sessions, with a TDCS amplitude of 2 mAmps. During the tDCS session, individuals will perform a 10-min computerized Go-No Go task

Certain randomly assigned participants will receive Sham Stimulation to the DLPFC for 8 daily 20-min sessions. The Sham stimulation is an inactive form of stimulation. During the sham brain stimulation session, individuals will perform a 10-min computerized Go-No Go task

Outcomes

Primary Outcome Measures

Change in Yale Food Addiction Scale scores
Yale Food Addiction Scale (YFAS26) that is a 25-item measure developed to measure food addiction. Score range: 0 to 7. Higher scores in the scale mean more symptoms resembling food addiction (worse).
Change in Three-Factor Eating Questionnaire scores
Three-Factor Eating Questionnaire is a validated scale that is designed to measure 3 dimensions of human eating behavior: cognitive restraint of eating (Factor I), disinhibition (Factor II), and hunger (Factor III). The minimum score for factors I-II-III is therefore 0-0-0, and maximum possible score is 20-16-15. Higher scores in the respective scales are indicative of greater cognitive restraint (better), uncontrolled (worse), or emotional eating (worse).

Secondary Outcome Measures

Change in brain neural activity by functional Magnetic Resonance Imaging ( fMRI)
Significant change in brain activity of the prefrontal cortex (area involved in the inhibitory control of food intake) measured by modification of BOLD (Blood-Oxygen-Level-Dependent) signal in fMRI evoked responses to visual food-cues
Change in Brain metabolites concentrations by Magnetic Resonance Spectroscopy (MRS)
Significant change in brain metabolites concentration at the prefrontal cortex (area involved in the inhibitory control of food intake) measured with Magnetic Resonance spectroscopy

Full Information

First Posted
April 21, 2017
Last Updated
June 3, 2020
Sponsor
University of California, Los Angeles
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1. Study Identification

Unique Protocol Identification Number
NCT04420767
Brief Title
The Effect of Brain Stimulation (tDCS) in Food Cravings Control in Overweight/Obese Women
Official Title
The Effect of Brain Neuromodulation on Food Cravings, Cognitive Control and Food Addiction Scales in Overweight/Obese Women Using tDCS
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 4, 2017 (Actual)
Primary Completion Date
May 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is a randomized clinical trial to test the effect of a type of non-invasive brain stimulation on the response to a behavioral intervention designed to enhance cognitive control over food cravings in obese and overweight women. The brain stimulation is called transcranial Direct Current Stimulation (tDCS). All eligible participants will engage in a behavioral intervention known to enhance control over food cravings and will be randomly assigned to receive either tDCS or sham stimulation to the prefrontal cortex of the brain.
Detailed Description
This study is a randomized clinical trial to test the effect of a type of non-invasive brain stimulation on the response to a behavioral intervention designed to enhance cognitive control over food cravings in obese and overweight women. The brain stimulation is called transcranial Direct Current Stimulation (tDCS) which is a form of stimulation that delivers a low amplitude electrical current to the brain via the scalp (i.e. trans-cranial) to modify brain activity. All eligible participants will engage in a behavioral intervention (Go-No Go task), known to enhance control over food cravings, and will be randomly assigned to receive either tDCS or sham stimulation to the right prefrontal cortex of the brain during 8 20-min daily sessions. Primary outcome: score changes in eating behaviors scales (YFAS and TFEQ), scales will be applied at baseline and at the end of the 8 brain stimulation sessions. Secondary outcomes: changes in diet, brain function (brain MRI/MRS) Other outcomes: food cravings scales and impulse control scales and cognitive function.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
food cravings, neuromodulation, brain, cognitive control, tDCS, prefrontal cortex, MRI, food addiction

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
tDCS and Go-No Go task
Arm Type
Experimental
Arm Description
Certain randomly assigned participants will receive tDCS to the DLPFC for 8 daily 20-minute sessions, with a TDCS amplitude of 2 mAmps. During the tDCS session, individuals will perform a 10-min computerized Go-No Go task
Arm Title
Sham brain stimulation and Go-No Go task
Arm Type
Sham Comparator
Arm Description
Certain randomly assigned participants will receive Sham Stimulation to the DLPFC for 8 daily 20-min sessions. The Sham stimulation is an inactive form of stimulation. During the sham brain stimulation session, individuals will perform a 10-min computerized Go-No Go task
Intervention Type
Device
Intervention Name(s)
tDCS
Other Intervention Name(s)
Real brain stimulation
Intervention Description
Individuals undergo 20min daily sessions receiving actual tDCS to the brain (to the right DLPFC: dorsolateral prefrontal cortex)
Intervention Type
Device
Intervention Name(s)
Sham brain stimulation
Intervention Description
Individuals undergo 20min daily sessions receiving sham stimulation to the brain (to the right DLPFC: dorsolateral prefrontal cortex)
Intervention Type
Behavioral
Intervention Name(s)
Go-No GO task
Intervention Description
During the brain stimulation sessions, all individuals will be asked to perform a 10 min-computerized task related to inhibitory control (Go-No Go)
Primary Outcome Measure Information:
Title
Change in Yale Food Addiction Scale scores
Description
Yale Food Addiction Scale (YFAS26) that is a 25-item measure developed to measure food addiction. Score range: 0 to 7. Higher scores in the scale mean more symptoms resembling food addiction (worse).
Time Frame
Scores measured at baseline and at up-to 2 weeks after the intervention
Title
Change in Three-Factor Eating Questionnaire scores
Description
Three-Factor Eating Questionnaire is a validated scale that is designed to measure 3 dimensions of human eating behavior: cognitive restraint of eating (Factor I), disinhibition (Factor II), and hunger (Factor III). The minimum score for factors I-II-III is therefore 0-0-0, and maximum possible score is 20-16-15. Higher scores in the respective scales are indicative of greater cognitive restraint (better), uncontrolled (worse), or emotional eating (worse).
Time Frame
Scores measured at baseline and at up-to 2 weeks after the intervention
Secondary Outcome Measure Information:
Title
Change in brain neural activity by functional Magnetic Resonance Imaging ( fMRI)
Description
Significant change in brain activity of the prefrontal cortex (area involved in the inhibitory control of food intake) measured by modification of BOLD (Blood-Oxygen-Level-Dependent) signal in fMRI evoked responses to visual food-cues
Time Frame
Brain function at baseline and up-to 2 weeks after the intervention
Title
Change in Brain metabolites concentrations by Magnetic Resonance Spectroscopy (MRS)
Description
Significant change in brain metabolites concentration at the prefrontal cortex (area involved in the inhibitory control of food intake) measured with Magnetic Resonance spectroscopy
Time Frame
Brain MRS at baseline and up-to 2 weeks after the intervention
Other Pre-specified Outcome Measures:
Title
Diet (3-day food intake record)
Description
3-day food intake record: individuals will record everything they eat and drink for 3 days. To assess calorie intake and macro nutrients
Time Frame
Values measured at baseline and at up-to 2 weeks after the intervention
Title
Change in Yale Food Addiction Scale scores at 3-months post-intervention
Description
Yale Food Addiction Scale (YFAS26) that is a 25-item measure developed to measure food addiction. Score range: 0 to 7. Higher scores in the scale mean more symptoms resembling food addiction (worse).
Time Frame
At 3-months after intervention
Title
Change in Three-Factor Eating Questionnaire scores at 3-months post-intervention
Description
Three-Factor Eating Questionnaire is a validated scale that is designed to measure 3 dimensions of human eating behavior: cognitive restraint of eating (Factor I), disinhibition (Factor II), and hunger (Factor III). The minimum score for factors I-II-III is therefore 0-0-0, and maximum possible score is 20-16-15. Higher scores in the respective scales are indicative of greater cognitive restraint (better), uncontrolled (worse), or emotional eating (worse).
Time Frame
At 3-months after intervention
Title
Cognitive function assessment
Description
Multiple Abilities Self-Report Questionnaire (MASQ), a self-report measure comprising items from five cognitive domains; language, visuo-perceptual, verbal memory, visual memory, and attention. The maximum score for the whole scale is 190 points. Higher scores correlate with better function.
Time Frame
Measured at baseline and up-to 2 weeks after the intervention

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: BMI between 28 and 40 kg/m2 high scores in the Yale-Food Addiction-Scale right-handed Exclusion Criteria: History of anorexia nervosa or bulimia or binge eating disorder Any contraindication to undergo MRI Use of psychotropic medications and/or opiate pain medications. Current or past alcohol or drug abuse problem or smoking Pregnancy Current use of weight loss medication or currently participating in a weight loss program. History of seizures, epilepsy or factors/medications associated with lowered seizure threshold. History of brain disease or major neurological disorder or mental disorder History of brain surgery or history of loss of consciousness >15 min History of major gastrointestinal surgery including weight loss surgery History of endocrine imbalances including diabetes, thyroid disease, Cushing's disease, metabolic syndrome and polycystic ovary.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claudia P Sanmiguel, MD
Organizational Affiliation
University of California, Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States

12. IPD Sharing Statement

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The Effect of Brain Stimulation (tDCS) in Food Cravings Control in Overweight/Obese Women

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