- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02227979
Effects of PURPLE Cry Intervention
April 7, 2016 updated by: James K. Rilling, PhD, Emory University
Biological Bases of Individual Variation in Paternal Nurturance
The proposed study is designed to investigate whether the PURPLE Crying program attains efficacy by optimizing the neural response in the anterior insula, and augmenting activity in regions of the brain known to be important for emotion regulation.
The aim is to determine the effects of the PURPLE Cry Intervention by investigating the following:
- independent variables that may affect a father's neural response to infant cries
- effects of the PURPLE cry intervention, compared to a control intervention, on fathers' reported aversiveness and empathy in response to cry stimuli
- effects of the PURPLE cry intervention, compared to a control intervention, on fathers' neural response to unknown infant cries compared to a tone control
- effects of the PURPLE cry intervention, compared to a control intervention, on fathers' neural responses to own infant cries compared to unknown infant cries
The investigators hypothesize:
- prior to the PURPLE material, fathers' neural responses to infant cry stimuli will be modulated by the following variables: subjective self-reported emotional reaction to cry stimuli, hormone levels, sleep quality and quantity, sex of the infant, infant temperament, life stressors, parental expectations, personality (neuroticism), and father's own childhood experience
- fathers who receive the PURPLE material compared to those that receive the control intervention will report a larger decrease in aversiveness and a larger increase in empathy in response to cry stimuli
- fathers who receive the PURPLE material compared to those that receive the control intervention will show a larger decrease in activity in the anterior insula and amygdala in response to cry stimuli
- fathers who receive the PURPLE material compared to those that receive the control intervention will show a larger increase in activity in regions of the brain important for emotion regulation, such as the dorsolateral prefrontal cortex (PFC) and orbitofrontal PFC
- fathers' neural activity in the amygdala in response to their own infant's cry stimuli will be positively correlated with both their own and infant testosterone levels
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
40 biological fathers of children age 2 months or younger who are currently cohabitating with the child's mother will be scanned on two separate occasions.
The optional second visit will occur after 2 months have passed since the first scan.
In the first visit, fathers will receive two MRI scans, one before and one after completing one of the two interventions.
Prior to the MRI scan, a blood sample will be collected for measurement of hormone levels.
Fathers will be positioned in the MRI scanner where they will receive structural and functional MRI scans of their brain while they listen to auditory stimuli: unknown cries, own cries, and tone controls.
Blood sample collection and intervention will not be conducted during the second visit.
Study Type
Interventional
Enrollment (Actual)
42
Phase
- Not Applicable
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
-
-
Georgia
-
Atlanta, Georgia, United States, 30322
- Emory University
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- biological fathers of children age 2 months or younger who are currently cohabitating with the child's mother
- fathers with normal or corrected-to-normal (with contact lenses) vision
Exclusion Criteria:
- history of head trauma, seizures or other neurological disorder
- psychiatric illness
- alcoholism or any other substance abuse
- serious medical illness
- claustrophobia
- ferrous metal in any part of body
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: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group I
The PURPLE Cry Intervention group will get an 11-page booklet and 12-minute DVD to review.
|
This intervention consists of an 11-page booklet and 12-minute DVD produced by the National Center on Shaken Infant Syndrome.
|
|
Active Comparator: Group II
The control intervention group will get 1 brochure and a DVD on infant safety to review.
|
This intervention consist of 1 brochure and a DVD on infant safety excerpted from the Safe Start video on infant safety.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in neural responses to infant cry stimuli
Time Frame: within one visit, pre and post PURPLE intervention, approximately 30 minutes apart
|
The effects of the intervention will be assessed by determining changes in neural responses between PURPLE Cry and Brochures treatments from functional magnetic resonance imaging (fMRI)
|
within one visit, pre and post PURPLE intervention, approximately 30 minutes apart
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in aversiveness and in empathy
Time Frame: within one visit, pre and post PURPLE intervention, approximately 30 minutes apart
|
The effects of the intervention will be assessed by determining changes in aversiveness and in empathy between PURPLE Cry and Brochures treatments by using Davis's Interpersonal Reactivity Index (IRI) and Beck Depression Inventory.
|
within one visit, pre and post PURPLE intervention, approximately 30 minutes apart
|
|
Change in neural activity in the anterior insula and amygdala during unknown infant cry
Time Frame: within one visit, pre and post PURPLE intervention, approximately 30 minutes apart
|
The effects of the intervention will be assessed by determining changes in activity in the anterior insula and amygdala between PURPLE Cry and Brochures treatments from functional magnetic resonance imaging (fMRI)
|
within one visit, pre and post PURPLE intervention, approximately 30 minutes apart
|
|
Change in neural activity in the dorsolateral prefrontal cortex (PFC) and orbitofrontal PFC
Time Frame: within one visit, pre and post PURPLE intervention, approximately 30 minutes apart
|
The effects of the intervention will be assessed by determining changes in activity in regions of the brain important for emotion regulation between PURPLE Cry and Brochures treatments from functional magnetic resonance imaging (fMRI)
|
within one visit, pre and post PURPLE intervention, approximately 30 minutes apart
|
|
Change in neural activity in the amygdala in response to their own infant's cry stimuli
Time Frame: within one visit, pre and post PURPLE intervention, approximately 30 minutes apart
|
The effects of the intervention will be assessed by determining changes in neural activity in the amygdala from functional magnetic resonance imaging (fMRI)
|
within one visit, pre and post PURPLE intervention, approximately 30 minutes apart
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: James K Rilling, Ph.D., Emory University
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
September 1, 2013
Primary Completion (Actual)
February 1, 2016
Study Completion (Actual)
February 1, 2016
Study Registration Dates
First Submitted
August 26, 2014
First Submitted That Met QC Criteria
August 26, 2014
First Posted (Estimate)
August 28, 2014
Study Record Updates
Last Update Posted (Estimate)
April 8, 2016
Last Update Submitted That Met QC Criteria
April 7, 2016
Last Verified
April 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB00044782a
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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