Role of Friends in Adolescent Interpersonal Relations
(BFFs Trial)
Trial Summary
What is the purpose of this trial?
The goal of this clinical trial is to investigate how the friendship experiences of maltreated (i.e., abused and/or neglected) and non-maltreated adolescents differentially influence their risk for adverse outcomes. The main questions it aims to answer are: 1. How do the friendships of maltreated adolescents differ from those of non-maltreated adolescents? 2. Which friendship experiences influence the associations between maltreatment and ability to regulate stress, as well as future mental health difficulties and revictimization? Participants will: * Attend the initial study visit on the campus of the University of South Carolina with their primary caregiver and a best friend during which they will: * Complete study questionnaires * Be connected to a device that records their physical ability to manage stress * Complete a task during which they will be audio and video recorded and complete a brief assessment rating how they are feeling at different times during task completion * Depending on which research group they are placed in, be assigned to discuss their experience doing this task with their friend (intervention group) or sit quietly in a room for 5 minutes (comparison group) * The follow-up study visit will involve completion of study questionnaires online or via mail 6 months later Additionally, the participant's caregiver and friend will complete study questionnaires. Researchers will compare the intervention group (debriefs with a friend) and comparison group (sits quietly for 5 minutes) to see if the presence of and discussion with the friend influences their physical ability to regulate stress and future outcomes.
Do I need to stop taking my current medications to join the trial?
The trial protocol does not specify whether you need to stop taking your current medications. It seems unlikely that you would need to stop, as the study focuses on friendships and stress regulation, not medication use.
What data supports the idea that Role of Friends in Adolescent Interpersonal Relations (also known as: Debrief) is an effective treatment?
The available research shows that friendships play a crucial role in adolescent development, helping with personal adjustment and social skills. For example, studies indicate that the quality of friendships, such as trust and communication, is linked to better coping mechanisms and social skills. Additionally, having a stable friendship network is associated with greater social satisfaction and school belonging. These findings suggest that focusing on friendships, as in the Role of Friends in Adolescent Interpersonal Relations treatment, can be beneficial for adolescents' social and emotional development.12345
What safety data exists for the treatment 'Role of Friends in Adolescent Interpersonal Relations'?
The provided research does not directly address safety data for the treatment 'Role of Friends in Adolescent Interpersonal Relations' or 'Debrief.' The studies focus on the influence of friendship networks on adolescent risk behaviors, peer influence on sexual risk behavior, and social influences on alcohol use. They highlight the importance of understanding peer relationships and social networks in shaping adolescent behaviors, which could inform the development of interventions. However, specific safety data or evaluations of the treatment itself are not mentioned in the research provided.678910
Is the treatment in the trial 'Role of Friends in Adolescent Interpersonal Relations' a promising treatment?
Yes, the treatment is promising because friendships play a crucial role in adolescent development. They help with emotional support, problem-solving, and building social skills. Friendships can also be used as a therapeutic tool to help troubled adolescents improve their mental health and social interactions.12111213
Eligibility Criteria
This trial is for adolescents aged 13-17 who have experienced maltreatment or not, with a non-offending caregiver and a best friend (not sibling/romantic partner) to participate. They must all be fluent in English. It excludes those without a non-offending caregiver, no best friend available, or not fluent in English.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Initial Study Visit
Participants attend an initial study visit with their caregiver and friend, complete questionnaires, undergo stress management assessment, and participate in a task with either a debrief or quiet sitting period.
Follow-up
Participants are monitored for changes in friendship, psychopathology, and revictimization experiences through questionnaires completed online or via mail.
Treatment Details
Interventions
- Debrief
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of South Carolina
Lead Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborator