Skip to content

Spatial and temporal dynamics of emotional memory consolidation

Spatial and temporal dynamics of emotional memory consolidation - Emotional memory

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON40617
Enrollment
96
Registered
2014-04-09
Start date
2014-06-23
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

traumatic memory and pathological fear

Interventions

In study arm 1, half of the subjects will undergo a stress induction protocol involving highly aversive cinematographic material and (threat of) mild electrical stimulation to the fingers. In the

Sponsors

Radboud Universiteit Nijmegen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: •Healthy volunteers between 18 and 45 years of age (balanced for gender) •Predominant right-handedness.

Exclusion criteria

Exclusion criteria: • Abnormal hearing or (uncorrected) vision. • Average use of more than 3 alcoholic beverages daily. • Average use of psychotropic medication or recreational drugs weekly or more. • Habitual smoking, i.e. more than a package of cigarettes per week and a self-reported inability or unease to cease smoking for 24 hours prior to testing. • Use of psychotropic medication, or of recreational drugs over a period of 72 hours prior to each test session, and use of alcohol within the last 24 hours before each measurement. • Regular use of corticosteroids. • Metal objects in or around the body (braces, pacemaker, metal fragments, hearing devices). • History of psychiatric treatment or current psychiatric treatment. • History of neurological treatment or current neurological treatment. • History of endocrine treatment or current endocrine treatment. • History of autonomic failure (e.g., vasovagal reflex syncope). • Current parodontitis (only in study arm 1). • Claustrophobia. • Intense daily physical exercise. • Irregular sleep/wake rhythm (e.g., regular nightshifts or cross timeline travel). • BDI score higher than 13.

Design outcomes

Primary

MeasureTime frame
Functional Magnetic Resonance Imaging (fMRI) Behavioural measures (e.g. memory accuracy and response bias)

Secondary

MeasureTime frame
Salivary levels of cortisol and alpha-amylase Psychophysiological recordings (pupil dilation, respiration, heart rate, skin conductance, blood pressure)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)