Comparison of Self and Clinician Administered Rating Scales in Patients With ADHD

NCT ID: NCT00711724

Last Updated: 2010-06-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-07-31

Study Completion Date

2009-03-31

Brief Summary

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The primary objective is to establish the concurrent validity of the clinician administered Attention Deficit Hyperactivity Disorder-Rating Scale (ADHD-RS) and the patient administered Attention Deficit Hyperactivity Disorder Self Report Scale (ASRS) v1.1 Symptom Checklist.

Detailed Description

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Conditions

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Attention-Deficit/Hyperactivity Disorder (ADHD)

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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MGH 1

Adolescents with Attention Deficit Hyperactivity Disorder (ADHD)

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of ADHD
* Age 13-65\* \*Parental consent and patient's assent will be obtained for minors participating in this protocol (only adolescents aged 13-18 yrs old will be included in the MGH site)

Exclusion Criteria

* Inability to reliably report ADHD symptoms at the discretion of the investigator
Minimum Eligible Age

13 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Massachusetts General Hospital

OTHER

Sponsor Role lead

Responsible Party

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Massachusetts General Hospital

Principal Investigators

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Paul Hammerness, MD

Role: PRINCIPAL_INVESTIGATOR

Massachusetts General Hospital

Locations

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Massachusetts General Hospital

Cambridge, Massachusetts, United States

Site Status

Countries

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United States

Related Links

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Other Identifiers

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2007-P-000911

Identifier Type: -

Identifier Source: org_study_id

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