NCT00592254

Unknown

Screening Protocol for Adults With ADHD

Massachusetts General Hospital Source

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Other study identifiers

Sponsor study identifier

2002-P-001856

Study Type

observational

Estimated enrollment

3,000

Locations

1 country

Sites

1

Timeline

Study Start

December 2002

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

December 2023

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Study Completion

December 2023

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Brief 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

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: unknown
Estimated enrollment: 3,000 participants
Study completion date: December 2023
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
December 2002
Date type not reported
This date has not been verified as actual or estimated.
First Submitted
December 28, 2007
Actual (reported)
First Posted
January 14, 2008
Actual (reported)
Primary Completion
December 2023
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.
Study Completion
December 2023
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.

Last Updated: January 18, 2022
Status Verified: January 2022
Last Update Submitted: January 14, 2022

Conditions

ADHD

Keywords

ADHDAdults

Outcome Measures

Primary Outcomes (1)

Screening Protocol
This study is a prescreening for possible entry into other studies
Sreening

Study Arms (1)

A

Eligibility Criteria

Age18 Years - 55 Years

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64)

Sampling MethodNon-Probability Sample

Study Population

Adults with symptoms of ADHD

You may qualify if:

Males and females ages 18-55

Sponsors & Collaborators

Massachusetts General Hospital
Otherlead

Study Sites (1)

Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

MeSH Terms

Conditions

Attention Deficit Disorder with Hyperactivity

Condition Hierarchy (Ancestors)

Attention Deficit and Disruptive Behavior DisordersNeurodevelopmental DisordersMental Disorders

Study Officials

Joseph Biederman, MD
Massachusetts General Hospital
PRINCIPAL INVESTIGATOR

Study Design

Study Type: observational
Observational Model: CASE ONLY
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Chief, Clinical and Research Programs in Pediatric Psychopharmacology and Adult ADHD

Study Record Dates

First Submitted

December 28, 2007

First Posted

January 14, 2008

Study Start

December 2002

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

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Phase 4Completed

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Phase 4Completed

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Phase 4Completed

NCT00585910

Study of Atomoxetine and OROS Methylphenidate to Treat Children and Adolescents Ages 6-17 With ADHD

Phase 4Completed

NCT00586573

Open-Label Pilot Study of Namenda in Adult Subjects With ADHD and ADHD NOS

Phase 4Completed

NCT00879320

Healthy Lifestyle in Adults With Attention Deficit Hyperactivity Disorder

Completed

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

You may not qualify if:

History of head trauma with loss of consciousness, organic brain disorders, seizures, or neurosurgical intervention.
Any significant medical condition, in the judgment of the investigator
Mental retardation
Pregnancy of lactation
Subjects with a known recent history (within the past 6 months) of illicit drug or alcohol dependence
Sensory difficulties such as deafness or blindness

Contact the study team to confirm eligibility.

December 2023

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Study Completion

December 2023

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Last Updated

January 18, 2022

Record last verified: 2022-01

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT00592254
Data provider: ClinicalTrials.gov
Source updated: 2022-01-18
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:35:32 UTC

Locations

US(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Study Arms (1)

A

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Related Links

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations