- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00879320
Healthy Lifestyle in Adults With Attention Deficit Hyperactivity Disorder
October 21, 2013 updated by: Thomas J. Spencer, MD, Massachusetts General Hospital
Healthy Lifestyle in Adults With ADHD
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).
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
253
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Massachusetts
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Cambridge, Massachusetts, United States, 02138
- Massachusetts General Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Adults ages 18-55 who have ADHD (for ADHD group) Healthy adult volunteers ages 18-55 who do not have ADHD (control group)
Description
Inclusion Criteria:
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.
Exclusion Criteria:
- Diagnosis of any psychotic disorder or Autism.
- Mental impairment as evidenced by a Full Scale I.Q. less than 80.
- Major sensorimotor handicaps such as deafness or blindness.
- Subject currently taking antipsychotic medication or mood stabilizers.
- Inadequate command of the English language.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
|---|
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1
Adults with ADHD
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2
Healthy adults without ADHD
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
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.
Time Frame: 1 time
|
1 time
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2009
Primary Completion (Actual)
May 1, 2012
Study Completion (Actual)
May 1, 2012
Study Registration Dates
First Submitted
April 9, 2009
First Submitted That Met QC Criteria
April 9, 2009
First Posted (Estimate)
April 10, 2009
Study Record Updates
Last Update Posted (Estimate)
October 22, 2013
Last Update Submitted That Met QC Criteria
October 21, 2013
Last Verified
October 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2008-P-002056
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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