NCT06160050 · University of Vermont
PRESERVE & CONNECT: Impact Study of the BPC
((BPC))
What this study is about
The PRESERVE \& CONNECT project is a multi-site randomly assigned control trial of the Breakthrough Parenting Curriculum: Navigating Trauma Across Generations (BPC) in rural and racially and ethnically diverse communities in Vermont and Connecticut.
View original scientific description
The PRESERVE \& CONNECT project is a multi-site randomized control trial of the Breakthrough Parenting Curriculum: Navigating Trauma Across Generations (BPC) in rural and racially and ethnically diverse communities in Vermont and Connecticut.
Interventions
BEHAVIORAL
Breakthrough Parenting Curriculum: Transforming trauma across generations
The BPC (Breakthrough Parent Curriculum): Navigating Trauma Across Generations is a 10 module course adapted from the NCTSN training called Caring for Children Who Have Experienced Trauma: A Workshop for Resource Parents (RPC). The BPC is specifically designed for parents who have been involved with (or are at risk for being involved with)the child welfare system. The course provides information about the impact of trauma on the development, attachment, emotions and behaviors of children while holding space for parents to learn together about concrete strategies for managing daily and ongoing challenges and enhancing their relationships with their children. All while acknowledging the challenges of parenting a child who has experienced trauma, while having experienced your own trauma.
Primary outcome measures
Child Safety
Time frame: up to 6 months
substantiated reports of child maltreatment as per administrative records
Child Permanency
Time frame: up to 6 months
out of family placements and placement disruptions as per administrative records. Total amount of each type of placement.
Child Well-being
Time frame: 10 weeks
behavioral and emotional functioning of their children (Strength and Difficulties Questionnaire).
Parenting Self-Efficacy Scale
Time frame: 10 weeks
Scores range from 0-160. Higher scores indicate more self efficacy
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- \- Parents involved in, or at risk of involvement in, the child welfare system.
Exclusion criteria
- active psychosis without medication stabilization
- ongoing major depressive episodes
- active suicidal ideation
- active homicidal ideation
Where
- Hartford, Connecticut
- Burlington, Vermont
Collaborators
University of Connecticut
Related conditions & keywords
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Apr 17, 2025 · Source of record for eligibility and locations