Clinical Trials Directory

Trials / Completed

CompletedNCT04312945

Affective Social Buffering

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
202 (actual)
Sponsor
University of Minnesota · Academic / Other
Sex
All
Age
11 Years – 14 Years
Healthy volunteers
Accepted

Summary

The purpose of this experiment is to determine the mechanisms through which parental buffering of stress physiology during affective stimulus presentation diminishes with pubertal development and whether this diminution of effectiveness extends to social buffering by peers (best friends), in comparison to a lack of social partners.

Detailed description

On visit one, the participant will complete questionnaires, including ones on pubertal development, screening for MRI safety, and quality of relations with parents and friends. Within 2 weeks the participant will return to the University where they will undergo the following protocol. Participants will be randomly assigned to one of 3 conditions that differ by who is with them in the scanner room: Primary Parent, Close Friend, No Social Partner. (N=50 per condition, 25 male, 25 female). Once at the Center for Magnetic Resonance Research, participants and the individual who will be with the participant in the scanning room will undergo an MRI safety screening (the repeat of what was completed over the phone). Females will be shown to a changing room where the investigators will privately question them about any possibility of pregnancy. The participant will also have a chance to experience a simulated MRI in order to determine whether they will be comfortable in an actual MRI. Participants will be shown into the scanning control room and one more safety check will be performed before they enter the scanner room and the scanner. If they are in one of the social buffering conditions, the social buffering partner will also enter the scanning room and will sit to the side of the scanner. The scanning bed will then be moved into the barrel of the MRI machine. The participant will be wearing head phones to protect his/her hearing and to receive instructions from the control room. The participant will then complete two emotionally evocative paradigms. The investigators will use a 3T Siemens Prisma scanner with a standard 32-channel phased array head coil.

Conditions

Interventions

TypeNameDescription
OTHERQuestionnairesThe participant will complete questionnaires, including ones on pubertal development and quality of relations with parents and friends.
OTHERMRIWithin 2 weeks of the first study visit, the participant will return to the University where they will undergo MRI.

Timeline

Start date
2023-07-17
Primary completion
2025-02-17
Completion
2025-02-17
First posted
2020-03-18
Last updated
2026-01-23
Results posted
2026-01-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04312945. Inclusion in this directory is not an endorsement.