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.
Full Title of Study: “Effectiveness of Parent Specific Depression Education and Motivation on Intent to Seek Follow-Up Care for Potential Depression Symptoms”
- Study Type: Interventional
- Study Design
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Primary Purpose: Health Services Research
- Masking: Triple (Participant, Investigator, Outcomes Assessor)
- Study Primary Completion Date: October 2011
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.
- Behavioral: 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.
- 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.
Arms, Groups and Cohorts
- Experimental: 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.
- Active Comparator: 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.
Clinical Trial Outcome Measures
- Depression Follow-Up Care Seeking
- Time Frame: at 2 weeks
- Mothers’ self-reported attempts at obtaining follow-up services for emotional health or depression.
- Intention to Seek Depression Follow-Up Care
- Time Frame: at 2 weeks
- Three item scale measure of intention to seek care (any) for follow-up of positive depression screen.
Participating in This Clinical Trial
- 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.
- 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
Gender Eligibility: Female
Minimum Age: 18 Years
Maximum Age: 65 Years
Are Healthy Volunteers Accepted: No
- Lead Sponsor
- University of California, Davis
- Children’s Miracle Network
- Provider of Information About this Clinical Study
Clinical trials entries are delivered from the US National Institutes of Health and are not reviewed separately by this site. Please see the identifier information above for retrieving further details from the government database.