Transmission of Mother-Infant Stress Communication

NCT ID: NCT02013401

Last Updated: 2018-10-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

56 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-10-31

Study Completion Date

2016-07-14

Brief Summary

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The central aim of this study is to assess mother-infant communication via behavioral, physiological, and affective indices under conditions where distal stressors may not be directly detectable by the infant.

Detailed Description

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This investigation examines a distal maternal stressor on the quality of interaction in mother-infant dyadic communication. Assessments include behavioral, physiological, and affective indices under conditions where distal stressors may not be directly detectable by the infant. The present research examines mother-infant interactions to test the hypothesis of whether maternal stress may be transduced to their infants via multiple pathways. The secondary aim is to explore effective emotion regulation strategies for the mother as potential buffers to stress and additionally reducing early life stress effects on the infant's regulatory development.

While the emotion regulation literature posits that reappraisal may be associated with decreased in physiological and psychological stress, this type of regulation strategy may be ineffective when interfacing with discrimination. The regulation strategy needs to be titrated to the stressor in order to be effective. These findings will have notable social, clinical, and psychological significance,

Conditions

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Stress

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

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Inclusion Criteria

* Healthy volunteers

Exclusion Criteria

* No presence of heart murmur or wear a pacemaker
* No medication for hypertensive or cardiovascular disease
* Not using beta blockers
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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University of Massachusetts, Boston

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Kymberlee O'Brien, PhD

Role: PRINCIPAL_INVESTIGATOR

Postdoctoral Research Fellow

Celia L Moore, PhD

Role: STUDY_DIRECTOR

Director of DSRC and Horizon Center

Edward Tronick, PhD

Role: STUDY_DIRECTOR

Director Child Development Unit

Locations

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University of Mass. Boston

Boston, Massachusetts, United States

Site Status

University of Massachusetts, Boston, Child Development Unit

Boston, Massachusetts, United States

Site Status

Countries

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United States

Other Identifiers

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2013173

Identifier Type: -

Identifier Source: org_study_id

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