Actively Recruiting
Stress Trajectories and Anhedonia in Adolescence Research Study
Led by University of North Carolina, Chapel Hill · Updated on 2025-06-27
192
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of North Carolina, Chapel Hill
Lead Sponsor
N
National Institute of Mental Health (NIMH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying how different biological responses in the brain and body relate to anhedonia, or the loss of pleasure, during adolescence. This study focuses on adolescents aged 13 to 15 years and aims to identify distinct patterns of brain and stress system activity that may influence the development and severity of anhedonia over time. The goal is to better understand how these biological factors contribute to emotional changes during adolescent development. Participants will complete evaluations at three timepoints: at the start of the study, at 10 months, and at 20 months. These assessments include psychological surveys completed remotely, cognitive tests conducted in person, brain imaging using functional MRI, and physiological measures such as heart rate variability and hormone levels from saliva samples. Participants will also engage in two behavioral stress tasks, the Montreal Imaging Stress Task and the Trier Social Stress Test for Children, which involve mental arithmetic and storytelling under evaluation. During the study, adolescents will complete various questionnaires and interviews, provide saliva samples, and participate in brain scans and stress tasks at each visit. Parents or legal guardians will also provide information through surveys. Researchers will measure outcomes such as anhedonia levels, brain activity changes, hormone responses, and nervous system function. The total study duration for each participant is 20 months, allowing observation of changes over time and careful monitoring of stress responses and pleasure experiences.
CONDITIONS
Brief Title
Stress Trajectories and Anhedonia in Adolescence Research Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 13-15 years old at study entry
- Ability to understand and sign an assent form
- Meets study hearing and vision requirements
You will not qualify if you...
- Current use of antipsychotic medication
- Current use of medications that would interfere with cardiovascular or endocrine assessments
- Metal in the body or other MRI exclusion
- Central nervous system disorder or brain injury that could confound brain imaging evaluations
- Presence of a medical condition that would interfere with cardiovascular or endocrine assessments
- Impaired intellectual functioning
- Diagnosed with a neurodevelopmental disability
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants complete initial psychological questionnaires remotely, cognitive assessments in-person, brain imaging, physiological measurements, and psychological interviews.
1 visit (combination of in-person and remote tasks)
Duration - 1 day
Participants complete psychological questionnaires remotely and in-person cognitive, brain imaging, physiological assessments, and stress tasks.
1 visit (combination of in-person and remote tasks)
Duration - 1 day
Participants complete psychological questionnaires remotely, cognitive assessments, brain imaging, physiological measurements, and a psychological interview.
1 visit (combination of in-person and remote tasks)
Trial Site Locations
Total: 1 location
1
University of North Carolina at Chapel Hill
Chapel Hill, North Carolina, United States, 27599
Actively Recruiting
Research Team
C
Clinical Research Coordinator
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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