Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
Healthy Volunteers
NCT07476469

tVNS and Approach-Avoidance Behavior in Anhedonia and Anxiety

Led by Dr. Nils B. Kroemer · Updated on 2026-04-23

104

Participants Needed

1

Research Sites

144 weeks

Total Duration

On this page

Sponsors

D

Dr. Nils B. Kroemer

Lead Sponsor

U

University of Bonn

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study investigates if anhedonia and anxiety symptoms are associated with alterations in reinforcement learning, effort trade-offs for wins vs. punishments, and foraging behavior under threat. Moreover, it will investigate whether these processes can be influenced by a metabolic load and/or transcutaneous vagus nerve stimulation (tVNS). The project consists of (a) an online reinforcement learning study, used to characterize learning, reward sensitivity, and meta-cognition, and (b) a laboratory study in which participants first undergo fMRI while completing an effort-based decision-making task. Second, participants will complete two sessions in VR with randomized active or sham tVNS during a foraging task before and after a caloric load with concurrent physiological recordings.

CONDITIONS

Official Title

tVNS and Approach-Avoidance Behavior in Anhedonia and Anxiety

Who Can Participate

Age: 18Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • BMI between 18.5 and 30.0 kg/m2
  • Age between 18 and 40 years
  • Able and willing to provide informed consent
Not Eligible

You will not qualify if you...

  • High risk of suicide
  • Lifetime diagnosis of severe neurological disorder (including ADHD), schizophrenia, bipolar disorder, severe substance abuse, posttraumatic stress disorder, obsessive-compulsive disorder, diabetes, epilepsy, or coronary heart disease
  • Diagnosis of eating disorder or somatic symptom disorder within the last 12 months
  • Taking medication other than stable psychopharmacological medication for major depressive disorder or anxiety (stable for at least two months before participation)
  • Contraindications for MRI such as metal implants or claustrophobia
  • Pregnant or nursing female individuals
  • Impaired movement ability or hearing
  • Impaired, uncorrected vision (need contact lenses)
  • Contraindications for tVNS such as hearing aids or diseased skin on the right ear

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital Bonn, Bonn, Germany

Bonn, Germany, 53127

Actively Recruiting

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Research Team

D

Dr. Anne Kühnel

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

4

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