Family Study of Affective and Anxiety Spectrum Disorders

StatusCompleted
PhaseNot specified
Started

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Record History

The 50 most recent of 339 record versions are accounted for below. See every version on ClinicalTrials.gov ↗

  1. Re-verified, no change to tracked fields
  2. Re-verified, no change to tracked fields
  3. New version filed on ClinicalTrials.gov
  4. 18 versions Re-verified since Nov 8, 2025, no change to tracked fieldsv319-v336
  5. Minor Trial status: Recruiting to Completed
    • Enrollment target: estimated 3975 to confirmed 1944
    v318
  6. 28 versions Re-verified since Oct 6, 2024, no change to tracked fieldsv290-v317
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This study will examine how depression, anxiety, and migraine run in families. It will help in defining the risk factors for physical, mental, and health problems-as well as define ways that those problems may be prevented and treated. A broad range of ages among family members will be included to evaluate the patterns of how these disorders are expressed throughout people's lives. Children of all ages will be included, and those ages 8 to 17 will be interviewed directly. Assessments will be collected through criteria of the Diagnostic and Statistical Manual of Mental Disorders IV as well as the spectrum, or range, of mood disorders and co-existing conditions. A member of the study team will visit the participants at home or will do an interview by telephone. Participation will take approximately 3 to 4 hours. Children will complete questionnaires given by the research team as well as questionnaires that they will do by themselves. The questions will pertain to the children's health, including physical and mental health and medical history, social relationships, problems, skills, and ways of dealing with important or stressful issues in their lives. These questionnaires will take up to 1 hour to complete. Health history gathered from adult participants will pertain to height, weight, exercise, and general function. Women will be asked about the use of oral contraceptives, estrogen, and progesterone. In addition, there will be questionnaires on personality and temperamental traits, that is, behavior and impulsiveness. Questions will also involve social intuition, family and other environmental factors, general functioning, and basic demographics such as ethnicity, race, socioeconomic status, marital status, education level, and employment history. Families enrolled in this phase of the research will be invited to participate in the next phase. There would be follow-up to evaluate the development of mood disorders, subtypes, and syndromes across the lifespan. ...
Trial Details
NCT Number NCT00071786
Lead Sponsor National Institute of Mental Health (NIMH)
Conditions
(from sponsor)
Mood Disorders, Sleep Disorders, Migraine
Related terms Migraine Disorders, Mood Disorders, Sleep Wake Disorders
Enrollment 1,944 participants
Start Date
Updated on ClinicalTrials.gov