Parent Specific Depression Education and Motivation

NCT ID: NCT01453790

Last Updated: 2017-05-30

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

Clinical Phase

NA

Total Enrollment

104 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-04-30

Study Completion Date

2012-01-31

Brief Summary

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This project is an investigator-initiated, randomized-controlled trial of the effectiveness of written and verbal parent-specific depression education and motivational advice in increasing participants self-disclosed intention to seek follow-up care for possible depression symptoms. The control condition is written and verbal general depression education and advice. Hypothesis: the office-based experimental intervention of written and verbal parent-specific depression and emotional health education and motivational advice increases intention to seek follow-up services for emotional health or depression, when compared to written and verbal general depression education and advice.

Detailed Description

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Maternal depression is a common problem, debilitating for mothers and affecting parenting practices with negative effects on the behavior, development, and physical health of children. The value of identifying and treating maternal depression for child development and well-being is well documented. Unfortunately, there are multiple barriers to the recognition and treatment of maternal depression. This is particularly problematic in younger women, as they are less often seen for health care. The overall objective of this project is to test whether the uptake of follow-up recommendations for potential depression by mothers identified by screening in clinical settings is improved by parent-specific targetting of depression education and motivational advice.

Conditions

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Depressive Symptoms

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Parent-Specific Depression Education-Motivation

Mothers receive depression education (verbal and written) with messages targeted to parent status which are drawn from previous research. They also receive motivational messages at 2 days via telephone.

Group Type EXPERIMENTAL

Parent-Specific Depression Education and Motivation

Intervention Type BEHAVIORAL

Parent-specific written and verbal depression messages garnered from previous research were consolidated into a pamphlet and script, respectively. These are dispensed after randomization in the pediatric office. At two days, mothers in the experimental group receive a motivational telephone call.

General Depression Education

Mothers receive general depression education (verbal and written) which are drawn from previous research. They also receive attention control telephone calls at 2 days.

Group Type ACTIVE_COMPARATOR

General Depression Education-Motivation

Intervention Type BEHAVIORAL

General depression education messages were compiled and are delivered verbally (scripted) and written (JAMA Depression Patient Page) after randomization in the pediatric office. At 2 days, mothers in the comparison group receive an attention control telephone call.

Interventions

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Parent-Specific Depression Education and Motivation

Parent-specific written and verbal depression messages garnered from previous research were consolidated into a pamphlet and script, respectively. These are dispensed after randomization in the pediatric office. At two days, mothers in the experimental group receive a motivational telephone call.

Intervention Type BEHAVIORAL

General Depression Education-Motivation

General depression education messages were compiled and are delivered verbally (scripted) and written (JAMA Depression Patient Page) after randomization in the pediatric office. At 2 days, mothers in the comparison group receive an attention control telephone call.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Parent of a child between the ages of 2 days and 12 years who is a patient of the UC Davis Pediatric Clinic.
* Primary, female caregiver
* Feeling down, depressed, or hopeless or little interest or pleasure in doing things.
* Not currently receiving care from a mental health practitioner.
* Comfortable speaking English without an interpreter.

Exclusion Criteria

* Parent of a child younger than 2 days or older than 12 years.
* Dad, Foster parent, or other short term guardian.
* Currently in treatment with a mental health practitioner.
* Limited English Proficiency
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Children's Miracle Network

OTHER

Sponsor Role collaborator

University of California, Davis

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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UC Davis Medical Center, General Pediatrics

Sacramento, California, United States

Site Status

Countries

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United States

References

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Fernandez y Garcia E, Joseph J, Wilson MD, Hinton L, Simon G, Ludman E, Scott F, Kravitz RL. Pediatric-based intervention to motivate mothers to seek follow-up for depression screens: The Motivating Our Mothers (MOM) trial. Acad Pediatr. 2015 May-Jun;15(3):311-8. doi: 10.1016/j.acap.2014.11.008.

Reference Type DERIVED
PMID: 25906700 (View on PubMed)

Other Identifiers

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214808-7

Identifier Type: OTHER

Identifier Source: secondary_id

214808

Identifier Type: -

Identifier Source: org_study_id

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