Screening Protocol for Research Participants
ScreenProt
Screening Protocol for the Evaluation of Research Participants
3 other identifiers
observational
523
1 country
1
Brief Summary
The Screening Protocol is a system devised to evaluate potential research participants for National Institute on Drug Abuse/Maryland Psychiatric Research Center (NIDA/MPRC) studies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2009
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 8, 2009
CompletedFirst Posted
Study publicly available on registry
November 10, 2009
CompletedStudy Start
First participant enrolled
December 1, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2019
CompletedAugust 19, 2019
August 1, 2019
9.5 years
July 8, 2009
August 15, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Recruitment of participants into NIDA/MPRC protocols.
5 years
Secondary Outcomes (1)
Demographic characterization of drug users, non-users, and individuals with serious mental illnesses contacting NIDA/MPRC about research participation
5 year
Study Arms (1)
Screening
Screening Assessment battery. Specific to study(or studies) the individual is screening for.
Interventions
Possibly blood draws, urine samples, toxicology screens, computer-based and written psychological, psychiatric, and behavioral questionnaires and assessments.
Eligibility Criteria
Population will see an advertisement in the community and call the NIDA call center. If they appear to meet the qualifications for one or more NIDA/MPRC studies, they will be scheduled to be screened.
You may qualify if:
- Age 18 or older
- Ability to read and understand and answer questions posed.
You may not qualify if:
- Inability to provide valid informed consent
- Below Age 18, and above age 64.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Maryland Psychiatric Research Center
Catonsville, Maryland, 21228, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Deanna L Kelly, Pharm.D., BCPP
University of Maryland, College Park
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Deanna L. Kelly, PharmD., BCPP Professor of Psychiatry Director, Treatment Research Program (TRP)
Study Record Dates
First Submitted
July 8, 2009
First Posted
November 10, 2009
Study Start
December 1, 2009
Primary Completion
June 1, 2019
Study Completion
June 1, 2019
Last Updated
August 19, 2019
Record last verified: 2019-08