Actively Recruiting

Phase Not Applicable
Age: 13Years - 15Years
All Genders
Healthy Volunteers
ID07040449

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

Age: 13Years - 15Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Baseline Assessment

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)

10-Month Follow-up Assessment

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)

20-Month Follow-up Assessment

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

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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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