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Modulating Amygdala and dACC activity during reward volatility in affective decision-making v2

Modulating Amygdala and dACC activity during reward volatility in affective decision-making v2 - Modulating activity in affective decision making 2.0

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON61248
Enrollment
43
Registered
2026-03-03
Start date
2026-06-29
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Normal brain function Normal brain function

Interventions

Sponsors

Radboud Universiteit Nijmegen
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Between 18-40 years of age;Have the ability and agreement to provide informed consent in sound body and mind, and the ability to fulfil the study’s requirements.

Exclusion criteria

Exclusion criteria: You may not participate if any of the following points apply to you:Current or planned pregnancy; A history of serious head trauma or brain surgery;Having a cardiac pacemaker or intracardiac lines;Having an implanted neuro-stimulator;Having a cochlear implant;Having an implanted medication infusion device;Implanted metal devices or large ferromagnetic fragments in the head or upper body (excluding dental wire), or jewellery/piercing that cannot be removed;Use of a medical plaster that cannot or may not be taken off (e.g., nicotine plaster);Any current episodes of psychiatric or neurological disorders;Claustrophobia;Hearing problems or ringing in the ears;Suffer from epilepsy;Predisposition for fainting spells (syncope); Use of (prescription) medication interacting with neuromodulation;Skin disease or sensitivity at intended stimulation sites;Meet a minimum performance level on the task;Large calcifications in the acoustic focus or beam path. Further, it is important that you:Do not use recreational drugs in the 48 hours prior to participation;Do not consume more than four alcoholic units in the 24 hours prior to participation or any alcoholic units 6 hours prior to participation;Do not consume more than your typical intake of caffeine and nicotine.

Design outcomes

Primary

MeasureTime frame
During the task, participants' responses will control a joystick whosemovements will be recorded. These behavioural responses will be categorisedbased on in-session conditions and between-session stimulation conditions. Thisallows us to compare the difference in behavioural responses between each condition.

Secondary

MeasureTime frame
Cortical changes in oxygen usage will be mapped using fMRI during task performance. With this, we can map oxygen usage in brain areas including the ones that were shown to be involved by previous studies such as the Amygdala, dACC. This activity can then be related to between-session stimulation conditions and within-session task conditions.In addition to this, we will also use measures of autonomic arousal during the sessions such as respiratory activity, heart rate and electrodermal activity.

Countries

Netherlands

Contacts

Public ContactK.T. Zee

Radboud Universiteit Nijmegen

admin@fcdonders.ru.nl024-3610750

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jul 23, 2026