Role of Friends in Adolescent Interpersonal Relations
(BFFs Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to understand how friendships affect adolescents who have faced maltreatment (abuse or neglect) compared to those who haven't. Researchers seek to determine how these friendships influence stress management and potential mental health challenges. Participants will either discuss their stress experience with a friend or sit quietly, while researchers measure their stress responses. A debrief session will follow to discuss the experience. Teens aged 13 to 17, with or without a history of maltreatment, who can bring a best friend to the study, might be a good fit for this trial. As an unphased trial, this study offers a unique opportunity to contribute to understanding adolescent friendships and mental health.
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 prior data suggests that this protocol is safe for adolescents?
Research shows that spending time with friends can help teenagers manage stress. One study found that friendships can lower stress levels, especially for those who have had tough childhoods. This suggests that talking with friends might be an effective way to handle stress.
In this trial, the treatment involves discussing issues with a friend. No physical risks have been associated with this activity. The focus is on understanding emotional and social support, which is generally safe. Studies on similar friendship interactions have not reported any negative effects.12345Why are researchers excited about this trial?
Researchers are excited about this trial because it explores how social support from friends can impact stress recovery in adolescents. Unlike typical stress management techniques that focus on individual coping strategies or medication, this approach investigates interpersonal interactions as a potential tool for improving emotional well-being. By using real-time psychophysiological monitoring and analyzing friend interactions, the trial aims to uncover the specific behaviors that might help reduce stress responses, potentially offering a new, accessible way to support adolescents' mental health.
What evidence suggests that this trial's debriefing treatment could be effective for stress regulation in adolescents?
Research has shown that friendships help young people manage stress more effectively. One study found a link between having good friends and better mental health, with less stress in the brain. Another study showed that supportive friends can reduce feelings of anxiety and depression. Evidence also suggests that friends can lower the body's stress reactions, potentially preventing future mental health problems. In this trial, participants in one arm will debrief with a friend after a stressful event, which may help them manage stress and improve their well-being in the future.678910
Are You a Good Fit for This Trial?
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 for a Trial Participant
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.
What Are the Treatments Tested in This Trial?
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