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Genetic and Neural Predictors of Adolescent Depression

Mass General Brigham logo

Mass General Brigham

Status

Unknown

Conditions

Major Depressive Disorder

Study type

Observational

Funder types

Other

Identifiers

NCT01743716
2012P002351

Details and patient eligibility

About

This study aims to examine the relationship between mood and brain activity in adolescent girls in order to better understand the genetic and neural predictors of adolescent depression. The participants in this study will be healthy female adolescents aged 12-14 and their mothers. They will participate for a total of six months. Adolescent participants will have three study sessions at McLean Hospital, and during two of them, their mothers will also have assessments. Adolescent assessments will include interviews, questionnaires, computer tasks, and collection of a saliva sample for genetic analyses. Their second study visit will include an fMRI scan. Parent assessments will include an interview, questionnaires, and a computer task.

Enrollment

100 estimated patients

Sex

Female

Ages

12+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Adult Cohort

A. MDD Mothers Cohort Inclusion Criteria:

  • Current or past Major Depressive Disorder
  • English as first language or English fluency
  • Biological daughter who meets inclusion/exclusion criteria for High Risk Female Adolescent

B. Healthy Control Mothers Cohort Inclusion Criteria:

  • No history of psychopathology
  • English as first language or English fluency
  • Biological daughter who meets inclusion/exclusion criteria for Healthy Female Adolescent

Adolescent Cohort

General Inclusion Criteria for Adolescent Cohorts:

  • Female
  • Ages 12-14
  • English as first language or English fluency
  • Right handed

General Exclusion Criteria for Adolescent Cohorts:

  • Past or present diagnosis of Major Depressive Disorder

  • Past or present diagnosis of any anxiety disorder

  • Past or present diagnosis of Bipolar Disorder

  • Past or present diagnosis of ADHD

  • Presence of medical or neurological illness (head injury, loss of consciousness greater than 5 minutes, seizure)

  • Current use of psychotropic medication

  • Presence of any contraindication for MRI:

    • Cardiac pacemakers
    • Metal clips on blood vessels (also called stents)
    • Artificial heart valve, artificial arms, hands, legs, etc.
    • Brain stimulator devices
    • Implanted drug pumps
    • Ear or eye implants
    • Known metal fragments in eyes
    • Exposure to metal filings or shrapnel (sheet metal workers, welders, and others)
    • Other metallic surgical hardware in vital area
    • Certain tattoos with metallic ink
    • Certain IUDs containing metal
    • Certain transdermal (skin) patches such as:
  • NicoDerm (nicotine for tobacco dependence)

  • Transderm Scop (scopolamine for motion sickness)

  • Ortho Evra (birth control)

    • Positive urine pregnancy test

C. High Risk Female Adolescent Additional Inclusion Criterion:

• Biological daughter of participant in the MDD Mothers cohort

D. Healthy Female Adolescent Additional Inclusion Criterion:

• Biological daughter of participant in the Healthy Control Mothers cohort

Trial design

100 participants in 4 patient groups

MDD Mothers
Description:
Adult women with a history of major depressive disorder (MDD) and a healthy adolescent daughter between the ages of 12-14
Healthy Control Mothers
Description:
Adult women with no history of psychopathology and an adolescent daughter between the ages of 12-14
High Risk Female Adolescents
Description:
Healthy female adolescents aged 12-14 with a mother in the MDD Mothers cohort
Healthy Female Adolescents
Description:
Healthy female adolescents aged 12-14 with a mother in the Healthy Control Mothers cohort.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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