- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02517060
Neural Mechanisms of Tactile Priming on Social Perceptions - Pilot Study
Study Overview
Status
Conditions
Detailed Description
Brain responses of healthy participants were recorded with functional magnetic resonance imaging (fMRI). While being scanned participants were asked to recommend punishments similar to judges or juries for perpetrators across different scenarios. In addition, participants were primed before reading the scenario by using different materials. Based on recent theories about "embodied cognition" and extralegal factors investigators hypothesize that those primes may influence the harshness of punishments recommended by the participants. If those processes engage sensorimotor cortices, the results would strongly support theories of embodied cognition.
The results would help the investigators to understand the neural correlates of priming processes. These unconscious complex processes of perception may be important for hospital patients. Thus, beneficial haptic experiences during the hospital stay may contribute to successful recovery.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Berlin, Germany, 12247
- Medical School Berlin
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Berlin, Germany, 10117
- Department of Psychiatry und Psychotherapy, CCM, Charité - University Medicine Berlin
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Berlin, Germany, 13353
- Department of Anesthesiology and Intensvie Care Medicine CVK/CCM, Charité - University Medicine Berlin
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- male or female healthy participants
- age 18 - 40 years
Exclusion Criteria:
- cardiac pacemaker
- metallic implants
- ferromagnetic parts in / at the body
- tatoos
- vessel surgery
- tinnitus
- epilepsia
- claustrophobia
- pregnancy
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Healthy participants
Male or female healthy participants
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Sensorimotor brain activation
Time Frame: The participantes will be followed up for the duration of fMRI-scan, an exspected average of 1 hour
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The primary objective of this study is to examine neural correlates for embodied cognitions.
We use an fMRI-approach to test if healthy participants are prone to non-conscious tactile priming effects during evaluation processes.
Investigators measure the outcome by examining BOLD Response in the sensorimotor cortices (Maximum Peak in Primary somatosensory Cortex, SI).
BOLD Responses will be analyzed using the Software SPM 8.
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The participantes will be followed up for the duration of fMRI-scan, an exspected average of 1 hour
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Systematic changes for evaluation processes
Time Frame: The participants will be followed up for the duration of fMRI-scan, an exspected average of 1 hour
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1. We examine if tactile priming leads to systematic behavioral changes for evaluation processes.
During the fMRI participants were asked to read scenarios and subsequently perform evaluation processes on a likert scale 0 to 5 (0 = mild punishment; 5 = hard punishment) .
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The participants will be followed up for the duration of fMRI-scan, an exspected average of 1 hour
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Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- SozPrime
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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