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Clinical Trials/NCT04420650
NCT04420650CompletedNot Applicable

Improving Insulin Sensitivity by Non-invasive Brain Stimulation

University Hospital Tuebingen1 site in 1 country44 target enrollmentStarted: May 26, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
44
Locations
1
Primary Endpoint
Peripheral insulin sensitivity

Study Overview

Brief Summary

Efforts in curing and preventing obesity and type 2 diabetes (T2D) have been elusive thus far. One reason for that is the lack of understanding of the role of the brain in the development and treatment of the disease. In recent studies, the hypothalamus was identified as part of a brain network including higher cognitive regions that is particularly vulnerable to insulin resistance. Furthermore, the central insulin response in this network predicted food craving and hunger. In this project, transcranial direct current stimulation (tDCS) is implemented as a tool to stimulate brain networks. The investigators hypothesize that stimulating the hypothalamus-cognitive network will enhance insulin sensitivity and reduce food intake, food craving and hunger. Furthermore, the project will provide the unique opportunity to investigate novel mechanisms of insulin resistance in participants who have been extensively metabolically characterized.

Detailed Description

Objectives The overarching aim of the study is to stimulate the hypothalamus-cognitive brain network to improve insulin sensitivity and eating behavior.

Specific Objectives

  1. Implement tDCS stimulation compared to sham stimulation in overweight and obese adults to assess the impact on eating behavior, cognition and metabolism.
  2. Evaluate whether 3-day non-invasive brain stimulation of the hypothalamus-cognitive network has a causal effect on metabolism.
  3. Evaluate whether 3-day non-invasive brain stimulation has a significant effect on brain functional connectivity and diffusion parameters.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
20 Years to 66 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Body mass index (BMI) between 25.5 and 39.5 kg/m2
  • •Age between 20 to 66 years of age
  • •Waist circumference ≥ 80 cm for women, ≥ 94 cm for men

Exclusion Criteria

  • •Insufficient knowledge of the German language
  • •Persons who cannot legally give consent
  • •Pregnancy or lactation
  • •History of severe mental or somatic disorders including neurological diseases (incl. epileptic seizures)
  • •Taking psychotropic drugs
  • •Previous bariatric surgery
  • •Acute infection within the last 4 weeks
  • •Hemoglobin values less than 12g/dl for women, less than 14 g/dl for men
  • •Current participation in a lifestyle intervention study or a pharmaceutical study
  • •Contradictions to a MRI measurement (e.g. metal implants)

Arms & Interventions

Cathodal tDCS

Active Comparator

Cathodal tDCS of the hypothalamus-cognitive network

Intervention: transcranial direct current stimulation (Device)

Anodal tDCS

Active Comparator

Anodal tDCS of the hypothalamus-cognitive network

Intervention: transcranial direct current stimulation (Device)

Sham Stimulation

Sham Comparator

Double blind sham stimulation (ramp-up ramp-down stimulation will be applied in order to simulate the active condition without any further continuous administration of current)

Intervention: transcranial direct current stimulation (Device)

Outcomes

Primary Outcomes

Peripheral insulin sensitivity

Time Frame: 1 day after last intervention tDCS day

Oral glucose tolerance derived insulin sensitivity based on the Matsuda index

Caloric intake (kcal)

Time Frame: 1 hour directly after tDCS stimulation

Free-choice, ad libitum food intake from a standardized breakfast buffet. The caloric intake from fat, carbohydrates and protein will be documented.

Change in subjective feeling of hunger and food craving

Time Frame: 5 minutes before tDCS stimulation, 5 minutes after tDCS stimulation and 5 minutes after buffet

On a visual analogue scale, subjective feeling of hunger and food craving will be assessed using a questionnaire.

Secondary Outcomes

  • Performance during stop-signal task(task is performed during 25-minutes tDCS stimulation)
  • Food choice(task is performed immediatly after buffet)
  • Functional connectivity(10 minutes functional MRI measurement performed before and after three day tDCS stimulation)
  • Tastiness and healthiness rating of food stimuli(task is performed immediatly after buffet)
  • Diffusion-weighted imaging(15 minutes MRI measurement performed before and after three day tDCS stimulation)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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