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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03282448
Other study ID # 29987
Secondary ID UL1TR001086
Status Completed
Phase N/A
First received
Last updated
Start date May 26, 2017
Est. completion date June 13, 2018

Study information

Verified date June 2018
Source Dartmouth-Hitchcock Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This pilot study will explore the feasibility and acceptability of implementing a family-based treatment, using HIPAA-compliant video-based communication technology, for adolescents (pregnant and post-delivery) with peripartum depressive symptoms within the context of home visiting.


Description:

The purpose of the pilot study is to partner with two Federal Maternal, Infant and Early Childhood Home Visiting (HV) Program sites to implement a family-based treatment for depression, using HIPAA-compliant video-based communication technology, in adolescent mothers (pregnant and post-delivery). This implementation-effectiveness hybrid trial includes depressed adolescent mothers and their adult family members.

It has three aims:

1. Explore the feasibility of integrating the treatment model into two Federal HV Program sites in New Hampshire.

2. Test the acceptability of the treatment model among depressed adolescent mothers and their families.

3. Explore preliminary impacts of the treatment on maternal depressive symptoms and parenting attitudes, family emotion regulation, and family functioning at two months post-intervention.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date June 13, 2018
Est. primary completion date June 13, 2018
Accepts healthy volunteers No
Gender All
Age group 13 Years to 25 Years
Eligibility Home Visitor Inclusion Criteria:

1. Willingness to participate in the study;

2. Intention to remain in current job for at least 12 months; and

3. Fluency in English: The training, treatment model, implementation meetings, and supervision sessions will be carried out in English.

Family Inclusion Criteria:

1. Adolescent mothers, ages 13-25, in the first trimester of pregnancy through eighteen months postpartum;

2. Adolescent mothers with Edinburgh Postnatal Depression Scale scores of =8;

3. At least one of the adolescent mother's family members ("family member" is defined as a person she is biologically related to, or significant close others/partners with whom she is not biologically related) must be willing and available to participate in eight of the 10 video-based family therapy sessions;

4. Fluency in English: The treatment will be carried out in English; and

5. Consistent internet access (i.e., subscribe to an internet service provider and do not experience weekly disruptions in service) on a cell phone, tablet, or computer equipped with a camera and microphone.

Family Exclusion Criteria:

Adolescent mothers with

1. A current positive screen for problem alcohol use on the CAGE or TWEAK;

2. A current positive screen on the drug abuse items on the home visiting interview;

3. A current positive screen for domestic violence on the Relationship Assessment Tool;

4. Current hallucinations and/or delusions;

5. Current homicidal ideation;

6. Current suicidal ideation;

7. Current severe major depressive episode as measured by the SCID-V Depression Module for those over age 18, or NIMH DISC-Y & DISC-P Mood Module for those under age 18; and/or

8. Current self-injurious behavior (e.g., cutting arms on a weekly basis). Families with

9. Current Child Protection Service involvement;

10. Current family therapy service involvement; and/or

11. Current or previous Dialectical Behavior Therapy (DBT) treatment.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
family therapy
The family-based intervention is informed by Dialectical Behavior Therapy Skills Training for Adolescents (Rathus & Miller, 2014).

Locations

Country Name City State
United States TLC Family Resource Center Claremont New Hampshire
United States The Family Resource Center at Gorham Gorham New Hampshire

Sponsors (3)

Lead Sponsor Collaborator
Fallon P. Cluxton-Keller Dartmouth-Hitchcock Medical Center, National Center for Advancing Translational Science (NCATS)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Maternal depressive symptoms Depressive symptoms will be measured using the Beck Depression Inventory (BDI-II; Beck, Steer, & Brown, 1996) 5 months
Secondary Therapist-family working alliance Clinician rated, and maternal report and family member report. 2.5 months
Secondary Family Satisfaction Maternal report and family member report. 2.5 months
Secondary Parenting attitudes A reliable and valid self-report measure will be completed by mothers. 5 months
Secondary Emotion regulation A reliable and valid self-report measure will be completed by mothers and their family members. 5 months
Secondary Family functioning A reliable and valid self-report measure will be completed by mothers and their family members. 5 months
See also
  Status Clinical Trial Phase
Withdrawn NCT03949465 - rTMS for Peripartum Depression N/A