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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00592254
Other study ID # 2002-P-001856
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date December 2002
Est. completion date December 2023

Study information

Verified date January 2022
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective of this protocol is to establish a comprehensive screening process to evaluate the eligibility of potential adult subjects for appropriate ADHD clinical research studies


Description:

To address the needs of the large number of adults who contact the Adult ADHD Program at Massachusetts General Hospital annually, we have sought approval for several research studies aimed at evaluating critical components of the needs of this population. Potential participants for those studies present with a widely varied set of complaints not always discernable in a telephone screening interview. This state of affairs often makes it difficult to ask subjects to sign a specific protocol's consent form without obtaining additional clinical information. Because of this, we have potential subjects consent to undergo an in-depth clinical assessment that will allow them to be screened by a clinician for eligibility to a diverse clinical research program available to them.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 3000
Est. completion date December 2023
Est. primary completion date December 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: 1. Males and females ages 18-55 2. Subjects must have a DSM-IV or DSM-V diagnosis of ADHD, as determined by a clinical evaluation based on DSM-IV or DSM-V criteria Exclusion Criteria: 1. History of head trauma with loss of consciousness, organic brain disorders, seizures, or neurosurgical intervention. 2. Any significant medical condition, in the judgment of the investigator 3. Mental retardation 4. Pregnancy of lactation 5. Subjects with a known recent history (within the past 6 months) of illicit drug or alcohol dependence 6. Sensory difficulties such as deafness or blindness

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Screening Protocol This study is a prescreening for possible entry into other studies Sreening
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