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Effect of Transcranial Direct Current Stimulation (tDCS) and Probiotic Supplementation in Overweight Adults

Comparing the Effectiveness of Transcranial Direct Stimulation (tDCS) and Probiotic Supplementation on Risky Decision-making, Impulsivity, Self-control, and Food Selection in Overweight Adults

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06035718
Enrollment
60
Registered
2023-09-13
Start date
2023-03-01
Completion date
2024-09-30
Last updated
2023-11-28

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

Conditions

Overweight and Obesity

Keywords

transcranial direct current stimulation, obesity, overweight, impulse control

Brief summary

The aim of the current study is to investigate and compare the effectiveness of probiotic supplementation and tDCS stimulation on risky decision-making related to food choices in overweight people. Considering the relatively established communication and interaction between the gut-brain-microbiome axis, the investigators expect that transcranial direct current stimulation and probiotic supplementation can both improve decision-making (decrease risky and impulsive decisions) and increase self-control in overweight people.

Interventions

By a probiotic blend capsule a specific product is intended which contains the following: Lactobacillus rhamnosus Lactobacillus plantarum Lactobacillus casei Lactobacillus helveticus Lactobacillus acidophilus Lactobacillus bulgaricus Lactobacillus gasseri Bifidobacterium bifidum Bifidobacterium lactis Bifidobacterium breve Bifidobacterium longum Streptococcus thermophile Fructooligosaccharides (FOS).

DEVICEtDCS

Using a tDCS device, a mild direct electric current is going to be non-invasively administered to the brain using rubber electrodes placed over the scalp.

DEVICESham tDCS

Using a tDCS device, a mild direct electric current is going to be non-invasively administered to the brain using rubber electrodes placed over the scalp. At this arm the electric current will be applied for a very short time (30 s) after which the device will turn off, thus providing the initial tingling sensation over the scalp but not interfering with the ongoing brain activity.

Sponsors

University of Messina
CollaboratorOTHER
Tabriz University
CollaboratorOTHER
University of Tehran
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* BMI over 25 * Higher than normal fat level

Exclusion criteria

* Pregnancy * Breastfeeding * Smoking more than 10 cigarettes a day * Excessive consumption of alcohol * Suffering from chronic cardiovascular and kidney diseases * Chronic digestive diseases such as celiac disease, * Chronic inflammatory bowel diseases such as colitis, intestinal surgery, cancer, etc. * Suffering from acute and chronic diarrhea in the last one month * Taking antibiotics in two months before the start of the study, * Continuous use of prebiotic and probiotic products and drugs in one month before the start of the intervention * Frequent use of antibiotics during the last month before the start of the intervention * Taking weight loss medications and following a special slimming diet in the last 3 months before the intervention. * History of epilepsy and seizures, stroke, * Use of pacemaker * Presence of metal implanted in the scalp or brain, * Presence of skin lesions at the tDCS stimulation site, and history of head injury or brain surgery. * Brain disorders and long-term and chronic use of neuropsychiatric drugs.

Design outcomes

Primary

MeasureTime frameDescription
Body analysis testDepending on the experimental group: 10 stimulation days in tDCS groups and 30 days in the probiotic group.This is a technique to determine the percentage of body mass that is fat compared to muscle. It can also indicate where the fat and muscle are carried within the body.
Impulsive Behavior Scale Questionnaire measuring Urgency, Premeditation (lack of), Perseverance (lack of), and Sensation seeking (UPPS)Depending on the experimental group: 10 stimulation days in tDCS groups and 30 days in the probiotic group.This is a self-report tool that assesses five subscales (urgency, premeditation, perseverance, sensation seeking, and positive urgency) that are used to measure five distinct dimensions of impulsive behavior; each scale ranging from 4 to 16); Higher scores represent worse outcome.
Eating attitudes Test (EAT-26)Depending on the experimental group: 10 stimulation days in tDCS groups and 30 days in the probiotic group.This tool is used to identify the presence of eating disorder risk based on attitudes, feelings and behaviours related to eating. The total score (between 0 and 78) provides an overall risk score, where higher scores indicating greater risk of an eating disorder.
Balloon analogue risk task (BART)Depending on the experimental group: 10 stimulation days in tDCS groups and 30 days in the probiotic group.BART is a computerized decision-making task that is used to assess risk-taking behavior. The BART simulates a real-world situation, involving actual risky behavior, where taking a risk up until a certain point yields a reward.
Tangney self-control questionnaire (Form 36)Depending on the experimental group: 10 stimulation days in tDCS groups and 30 days in the probiotic group.This is a self-report measurement to assess individual differences in traits of self-control. Scores range from 0 to 144 with higher scores representing worse outcome.

Countries

Iran

Contacts

Primary ContactAbed Hadipour Lakmehsari, PhD
ahadipourlakmehsari@unime.it3883041384

Outcome results

None listed

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