Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
Healthy Volunteers
NCT07198100

tVNS, Motivation, and Insulin Sensitivity

Led by University of Bonn · Updated on 2025-12-24

120

Participants Needed

1

Research Sites

111 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Disturbances in energy metabolism significantly increase the risk of developing major depressive disorder (MDD), especially in individuals with type 2 diabetes. Insulin sensitivity may particularly impair reward anticipation and motivational processes, contributing to anhedonia, a core symptom of depression. Preclinical and clinical studies highlight the vagus nerve as a critical pathway mediating metabolic signals between the body and the brain, influencing motivational and affective states. The present study aims to evaluate whether acute transcutaneous auricular vagus nerve stimulation (taVNS) improves motivation and mood and whether individual differences in insulin sensitivity modulate these improvements. The investigators plan to recruit 60 patients with MDD and 60 control participants matched for age, sex, and body mass index (BMI), covering a wide BMI range (up to 40 kg/m²) and insulin sensitivity (including patients with type 2 diabetes). Participants will undergo comprehensive metabolic assessments, behavioral testing of reward anticipation, motivation, consummation, and learning, and ecological momentary assessments (EMA) coupled with continuous glucose monitoring to assess real-world motivational behavior and glucose dynamics. Furthermore, participants will undergo two neuroimaging sessions, involving both task-free and task-based functional MRI, during concurrent taVNS or sham stimulation, implemented in a randomized, single-blinded, crossover design. This study hypothesizes that individuals with lower insulin sensitivity, particularly those with MDD and pronounced anhedonic symptoms, will show greater motivational and neural responsiveness to taVNS. H1A. Individuals with depression (vs. controls) and higher anhedonia show greater deficits in reward-related behavior and lower insulin sensitivity. H1B. Across all participants, reduced reward-related behavior and higher anhedonia are associated with lower insulin sensitivity. H2A. tVNS (vs. sham) increases motivation for rewards, brain responses to rewards, and body-brain interactions across participants. H2B. These tVNS-induced effects are particularly pronounced in individuals with depression and stronger anhedonia who show reductions in these domains. H3A. Greater tVNS-induced effects (behavioral, neural, body-brain) are associated with lower insulin sensitivity.

CONDITIONS

Official Title

tVNS, Motivation, and Insulin Sensitivity

Who Can Participate

Age: 18Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants diagnosed with depression (DSM-5) or without depression (no lifetime DSM-5 diagnosis)
  • Body mass index (BMI) between 18.5 and 40 kg/m²
  • Age between 18 and 60 years
  • Provided legally valid informed consent
Not Eligible

You will not qualify if you...

  • History of brain injury
  • History of schizophrenia
  • History of bipolar disorder
  • History of severe substance use disorder
  • History of coronary heart disease
  • History of stroke
  • History of epilepsy
  • History of chronic inflammatory diseases (e.g., rheumatoid arthritis, Crohn's disease)
  • Diagnosis of type 1 diabetes
  • Diagnosis of obsessive-compulsive disorder within 12 months prior to the study
  • Diagnosis of somatic symptom disorder within 12 months prior to the study
  • Diagnosis of eating disorder within 12 months prior to the study
  • Control participants with history of depression
  • Control participants with history of anxiety disorders (except specific phobias)
  • Contraindications for MRI (e.g., metal implants, claustrophobia)
  • Contraindications for taVNS (e.g., piercings, sore or diseased skin on the outer right ear)
  • Pregnant or breastfeeding women
  • Unclear capacity to consent
  • History of stomach surgeries affecting body weight (e.g., bypass surgeries)

AI-Screening

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Trial Site Locations

Total: 1 location

1

Section of Medical Psychology, Department of Psychiatry & Psychotherapy, Faculty of Medicine, University of Bonn

Bonn, Germany, 53127

Actively Recruiting

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Research Team

N

Nils B Kroemer, Prof. Dr.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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