- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01939639
The Influence of Oxytocin on the Processing of Social Contact
September 5, 2013 updated by: Rene Hurlemann, University Hospital, Bonn
Social touch can convey the most potent and salient of socio-emotional signals.
While the hypothalamic peptide oxytocin (OXT) has been identified as a key neurochemical mediator of grooming in some other social species, its modulatory influence on human interpersonal touch is unknown.
The investigators expect that OXT augments the hedonic value of touch and that this behavioral effect is paralleled at the neural level by an increased response in brain areas mediating rewarding aspects of social touch.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
40
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
North Rhine-Westphalia
-
Bonn, North Rhine-Westphalia, Germany, 53105
- Department of Psychiatry, University of Bonn
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
Healthy male volunteers
Exclusion Criteria:
Current or past psychiatric disease Current or past physical illness Psychoactive medication Tobacco smokers
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Oxytocin
24 IU Oxytocin, intranasal application 30 min prior to the experiment
|
24 IU Oxytocin, intranasal application 45 min prior to the experiment
Other Names:
|
Placebo Comparator: Placebo
intranasal application, sodium chloride solution, 3 puffs per nostril
|
intranasal application, sodium chloride solution, 3 puffs per nostril
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pleasantness ratings of social touch
Time Frame: 30 minutes after the nasal spray administration
|
After each trial, subjects are asked to use a visual analog scale to rate the pleasantness of the administered touch.
|
30 minutes after the nasal spray administration
|
Blood-oxygen-level dependent signal in response to social touch
Time Frame: 30 minutes after the nasal spray administration
|
By using functional magnetic resonance imaging we want to examine oxytocin's effects on the neural correlates (BOLD signal) of social touch.
|
30 minutes after the nasal spray administration
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Questionnaire measurement of mood (PANAS) and anxiety (STAI).
Time Frame: 15 minutes before the nasal spray administration and (on average) 10 minutes after the fMRI experiment
|
15 minutes before the nasal spray administration and (on average) 10 minutes after the fMRI experiment
|
Other Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Saliva oxytocin concentrations
Time Frame: 15 minutes before the nasal spray administration and (on average) 10 minutes after the fMRI experiment
|
15 minutes before the nasal spray administration and (on average) 10 minutes after the fMRI experiment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2013
Primary Completion (Actual)
June 1, 2013
Study Completion (Actual)
August 1, 2013
Study Registration Dates
First Submitted
August 27, 2013
First Submitted That Met QC Criteria
September 5, 2013
First Posted (Estimate)
September 11, 2013
Study Record Updates
Last Update Posted (Estimate)
September 11, 2013
Last Update Submitted That Met QC Criteria
September 5, 2013
Last Verified
September 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- OXT_PS_2013
- PS_2013 (Other Grant/Funding Number: University of Bonn)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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