Biological Basis of Individual Variation in Social Cooperation

NCT01566539 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 707

Last updated 2017-09-25

Study results available
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Summary

The project has three overall objectives. The first is to determine whether and how administration of intranasal oxytocin (OT) and intranasal vasopressin (AVP) influence cooperative decision-making and neural responses to cooperative and un-cooperative social interactions. The second is to determine whether and how intranasal vasopressin influences subjective evaluations of and neural responses to same and opposite-sex face stimuli and to determine if any of these effects persist beyond the period of AVP exposure. The third objective is to determine if intranasal OT influences empathy-related behavior and associated brain activity.

Conditions

  • Healthy

Interventions

DRUG

Intranasal Oxytocin (OT) 24 IU

Participants will self-administer a single dose of 24 international units (IU) oxytocin. Five puffs per nostril, each with 2.4 IU oxytocin. Ten puffs total.

DRUG

Intranasal Vasopressin (AVP)

Participants will self-administer a 1 ml solution containing 20 units of AVP. Five puffs per nostril, each with 2 International Units (IU) AVP. Ten puffs total).

DRUG

Intranasal Placebo

Participants will receive placebo sprays that are pH adjusted to comparable levels of the drugs given. Five puffs per nostril; ten puffs total.

DRUG

Intranasal Vasopressin (AVP) 40 IU

Participants will self-administer a 0.5 ml solution containing 40 international units (IU) of AVP. 5 puffs in total, each with 4 International Units (IU) AVP.

DRUG

Lorazepam

Subjects will take 1.0 mg of lorazepam orally 60 minutes prior to fMRI scan.

Sponsors & Collaborators

  • National Institute of Mental Health (NIMH)

    collaborator NIH
  • John Templeton Foundation

    collaborator OTHER
  • Emory University

    lead OTHER

Principal Investigators

  • James K Rilling, Ph.D. · Emory University

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Max Age
30 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-04-30
Primary Completion
2016-11-30
Completion
2016-11-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01566539 on ClinicalTrials.gov