跳至主要内容
临床试验/NCT00879320
NCT00879320已完成不适用

Healthy Lifestyle in Adults With ADHD

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 253 人开始时间: 2009年2月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
253
试验地点
1
主要终点
Comparison of ADHD and control subject health habits will be assessed by subject-rated questionnaires and health measures, such as vital signs and blood draw results.

研究概览

简要总结

The purpose of this study is to understand the relationship between ADHD and the overall health of someone with ADHD. People who have ADHD have trouble paying attention, concentrating, organizing, and planning. They may have trouble in school, at work, and at home. The investigators are interested in finding out whether these difficulties have had any influence in the past, current, or future health problems of someone with ADHD. About 100 people with ADHD and 100 people without ADHD will take part in this research study, all through Massachusetts General Hospital (MGH).

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • ADHD Subjects
  • Signed written informed consent to participate in the study.
  • Age: 18 - 60 (inclusive).
  • Current diagnosis of DSM-IV ADHD by structured interview. Late age of onset acceptable for participation provided ADHD symptoms meet full criteria currently.
  • Control Subjects
  • Signed written informed consent to participate in the study.
  • Age: 18 - 60 (inclusive).
  • Subjects must have <3 symptoms in each domain (Inattention and Hyperactive/Impulsive) and <5 total symptoms in both domains on the DSM-IVADHD module of the structured interview.

排除标准

  • Diagnosis of any psychotic disorder or Autism.
  • Mental impairment as evidenced by a Full Scale I.Q. less than
  • Major sensorimotor handicaps such as deafness or blindness.
  • Subject currently taking antipsychotic medication or mood stabilizers.
  • Inadequate command of the English language.

结局指标

主要结局

Comparison of ADHD and control subject health habits will be assessed by subject-rated questionnaires and health measures, such as vital signs and blood draw results.

时间窗: 1 time

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Thomas J. Spencer, MD

Associate Chief, Clinical and Research Program, Pediatric Psychopharmacology

Massachusetts General Hospital

研究点 (1)

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