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Transcranial Direct Current Stimulation for Impulsivity and Food-related Impulsivity in Obesity

Effect of Transcranial Direct Current Stimulation (tDCS) Applied Over the Orbitofrontal Cortex on Impulsivity and Decision Making in Obese Subjects

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04218383
Acronym
tDCS
Enrollment
30
Registered
2020-01-06
Start date
2020-02-03
Completion date
2022-11-01
Last updated
2021-01-15

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

Conditions

Impulsive Behavior

Brief summary

In this study the investigators aim to assess whether transcranial direct current stimulation (tDCS; a safe non-invasive method for modulating the activity of specific brain regions) when applied over the orbitofrontal cortex (OFC) is able to modulate impulsivity in obese participants.

Detailed description

In this single-blind, sham controlled study, the investigators will assess whether transcranial direct current stimulation (tDCS; a safe non-invasive method for modulating the activity of specific brain regions) when applied over the orbitofrontal cortex (OFC) is able to modulate impulsivity in obese volunteers. The investigators hypothesize that tDCS applied to the OFC, in comparison to sham tDCS, will significantly reduce impulsivity and enhance decision making as measured by computerized neurocognitive tasks. For this study the investigators will enroll 30 obese individuals aged 18-65 years. Participants will be assessed with a battery of computerized tasks as well as self-reported questionnaires on eating, impulsivity, mood and anxiety. Assessments will be carried out before, during, and after a single 20-minute 2mA tDCS session.

Interventions

DEVICETranscranial Direct Current Stimulation

Anode placed over the OFC and cathode placed over the right primary motor cortex.

Sponsors

University of Calgary
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Men or Women aged 18 to 65 * have body mass index of 35 or above * have had no recent change in medications in the 2 weeks prior participating in the study * able to fast for 4 hours prior participating in the study

Exclusion criteria

* Active Substance use disorder * Active Suicidal ideation * Psychoactive Medication * Past or current Gambling disorder * Past or current Anorexia * Past or current Bulimia Nervosa * Past or current Psychosis * Visual impairments preventing performance of the neuropsychological tasks * Epilepsy * Traumatic Brain Injury * Stroke * Neurological disorder affecting motor functions (Parkinsons, Huntington's, etc) * Previous participation in tDCS research/treatment

Design outcomes

Primary

MeasureTime frameDescription
Probabilistic Decision MakingBefore and after a 20-minute tDCS sessionNet score of the Iowa Gambling Task The net score ranges from -20 to 30. Higher values represent a better outcome (i.e., enhanced decision-making)

Secondary

MeasureTime frameDescription
Cognitive ControlBefore and after a 20-minute tDCS sessionInterference index in the Stroop Color-word Task. Interference index is the reaction time computed between the presentation of the stimulus and the response of the participant. It typically ranges from 0 to 300 millisecond, with smaller values of reaction time indicate better outcome (i.e., better cognitive control).
Food-specific cognitive controlBefore and after a 20-minute tDCS sessionThe interference index in the Food-Stroop Color-Word test. Interference index is the reaction time computed between the presentation of the stimulus and the response of the participant. It typically ranges from 0 to 300 millisecond, with smaller values of reaction time indicate better outcome (i.e., better Food-specific cognitive control).
Delayed discountingBefore and after a 20-minute tDCS sessionThe discount rate for delayed monetary rewards. This rate is quantified by the hyperbolic discounting function using the following equation: V = A/(1+kD), where A presents the value of the delayed reward A at delay D, and k is a free parameter that determines the discount rate, with higher values of k indicate worse outcome (i.e., greater discounting of rewards as a function of time).
Motor impulsivityBefore and after a 20-minute tDCS session.The stop-signal reaction time in the Stop-Signal Task. The stop signal reaction time ranges from 50 to 250, where greater values represent worse outcome (i.e, increased motor impulsivity).
Moderation of effect by self-reported measures of impulsivity and dysregulated eatingBefore and after a 20-minute tDCS session.Individuals with high levels of impulsivity, impulsive eating, binge eating, self-reported food addiction will show greater moderation by tDCS on our primary and secondary outcomes. Barrat's impulsiveness scale-11 with a range of scores from 0 to 120, with higher scores indicating greater impulsivity. Reward-based eating drive scale-13 with a range of scores from 0 to 54, with higher scores indicating greater uncontrolled eating. Binge eating scale with a range of scores from 0 to 46: minimal binge eating ( \>17), moderate binge eating (18-26), and severe binge eating (\<27)). Yale Food Addiction Scale with a range of symptom severity from 0 to 7: mild (2-3 symptoms), moderate (4-5 symptoms), severe (6 or more symptoms)).

Countries

Canada

Outcome results

None listed

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