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Completed Not applicable Interventional

Social Media, Teen Moms and PPD

ClinicalTrials.gov ID: NCT01967394

Public ClinicalTrials.gov record NCT01967394. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

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Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Social Media, Teen Moms, and Postpartum Depression

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Approximately 400,000 live births occur to adolescents in the United States annually. Of the 50% of adolescent mothers who experience depressive symptoms, less than 25% comply with referrals for depression evaluation and treatment due to lack of knowledge of depression symptoms (literacy), negative attitude towards mental health treatment, perception that individuals with depression are stigmatized (subjective norms), lack of understanding of health resources that are available to her and under her control (perceived control), and lack of time. Social media is a promising vehicle to reach and educate adolescent mothers since most adolescent mothers use social media for communication and to search for health information. Based upon the Theory of Planned Behavior, the investigators will target 11 counties in Kentucky with a social media ad campaign that will result in adolescent mothers (n=140) from those counties enrolling in an internet based intervention related to postpartum depression. The previously tested intervention includes vignettes from other adolescent mothers, questions and answers, resources, and an option to enroll in text message service. Before the intervention, after the intervention, and two weeks later the adolescent mothers will complete established questionnaires to determine if the intervention improved attitude and subjective norms towards depression and depression treatment, perceived control and intention related to seeking depression treatment, and the number of adolescent mothers with symptoms of depression who receive depression treatment. Data will be compared to scores on the same instruments from adolescent mothers (n=140) from the control group (18 other counties in Kentucky) that have not been targeted with the social media ad campaign or participated in the intervention. Data from the adolescent mothers in the control group will be collected in partnership with community agencies. The overall purpose of this trial is to test a cost effective and feasible method for reducing the cognitive and emotional barriers to accessing depression treatment in adolescent mothers. The specific aims are to (1) measure the extent to which a social media ad campaign is effective as a recruitment strategy; (2) test the effectiveness of an internet based social marketing intervention on both intention to seek treatment and rates of depression treatment, and (3) examine the dose effect of the intervention.

Study identification

NCT ID
NCT01967394
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
University of Louisville
Other
Enrollment
287 participants

Conditions and interventions

Eligibility (public fields only)

Age range
13 Years to 21 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2013
Primary completion
Nov 30, 2015
Completion
Nov 30, 2015
Last update posted
Dec 28, 2015

2013 – 2015

United States locations

U.S. sites
8
U.S. states
1
U.S. cities
8
Facility City State ZIP Site status
Three Rivers Carrollton Kentucky 41008
Hands Program of Kenton County (Young Families of Children, Inc) Covington Kentucky 41011
Lincoln Trail Health Department Elizabethtown Kentucky 42701
St. Joseph Hospital Lexington Kentucky
University of Louisville Hospital Louisville Kentucky
Hands Program of Boone and Campbell Counties (Every Child Succeeds) Newport Kentucky 41072-0325
Three Rivers Health Department Owensboro Kentucky 42303
Lake Cumberland Health Department Somerset Kentucky 42501

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01967394, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 28, 2015 · Synced Sep 5, 2026

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The complete protocol, eligibility criteria, and contact information for NCT01967394 live on ClinicalTrials.gov.

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