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Modulatory effects of instructions on extinction efficacy in appetitive and aversive learning

Modulatory effects of instructions on extinction efficacy in appetitive and aversive learning - InfExt

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00032460
Enrollment
150
Registered
2023-08-11
Start date
2023-08-14
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Heathy volunteers

Interventions

Group 1: The general procedure of the behavioral experiment consists of an acquisition training, extinction training, and reinstatement phase of a classical conditioning paradigm. We will combine geom

Sponsors

Universitätsklinikum Essen (AöR)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: - normal or corrected-to-normal vision with contact lenses - right-handedness

Exclusion criteria

Exclusion criteria: No fluency in German, BMI 30, chronic pain, severe diseases, or mental disorders, skin diseases, or skin damage, pregnancy or nursing, anisocoria, contraindication to MRI scans, allergic responses to cayenne pepper, previous participation in a fear conditioning study, and participation in any study investigating drug effects within the last three months, acute infection, pain at the study dates, engagement in professional sports at the study dates, consumption of psychoactive substances within 3h, or acute pain medication within 24 h before participation.

Design outcomes

Primary

MeasureTime frame
Development of expectancy ratings of CS-US-associations over the acquisition training, extinction training, and reinstatement test using a visual analogue scale with the anchors most probably cooling (-100), no change (0) and most probably heating (100).

Secondary

MeasureTime frame
Contingency ratings of CS-US coupling after each acquisition and extinction training, and reinstatement test, CS valence ratings before and after each phase, pain intensity and (un)pleasantness ratings of the US (temperature stimuli), electrodermal activity (skin conductance response) to CS and US, pupillometry to CS and US, resting state neural connectivity (rsfMRI).

Countries

Germany

Contacts

Public ContactKatharina Schmidt

Universitätsklinikum Essen

katharina.schmidt@uk-essen.de+492017232446

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 1, 2026