Screening Protocol for the Evaluation of Research Participants
Evaluation of Potential Research Subjects - Screening Protocol for Clinical Studies
2 other identifiers
observational
55,000
1 country
1
Brief Summary
Background: \- The National Institute on Drug Abuse (NIDA) uses a standardized set of procedures to develop a pool of potential participants for research studies. Because some of the data collected during screening are used later for research, the screening itself is considered a study. An applicant to any NIDA study is considered a participant in NIDA screening. Objectives: \- To identify, recruit, and screen participants for NIDA research protocols. Eligibility: \- Individuals 18 years of age and older who are able to provide informed consent. Design:
- Individuals who are eligible for screening will undergo two interviews: a telephone interview and an in-person interview. The phone interview will determine eligibility for the in-person interview.
- The in-person interview may require up to five visits to NIDA. The in-person visit will involve any or all of the following procedures: (1) full physical examination and medical history; (2) psychiatric interview; (3) psychological testing; (4) electrocardiogram; (5) samples of blood, urine, and hair; and (6) other minimally invasive procedures as directed by the research staff.
- During screening, a photograph will be taken for confirmation of identity during subsequent visits for other studies.
- No clinical care will be provided as part of screening.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2006
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
Study Start
First participant enrolled
May 17, 2006
CompletedFirst Submitted
Initial submission to the registry
December 18, 2009
CompletedFirst Posted
Study publicly available on registry
December 21, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
June 17, 2010
CompletedJuly 2, 2017
June 17, 2010
December 18, 2009
June 30, 2017
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- Adults (at least age 18)
- Ability to understand and answer the questions as posed.
You may not qualify if:
- \. Inability to provide valid informed consent.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Institute on Drug Abuse, Biomedical Research Center (BRC)
Baltimore, Maryland, 21224, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- NIH
Study Record Dates
First Submitted
December 18, 2009
First Posted
December 21, 2009
Study Start
May 17, 2006
Study Completion
June 17, 2010
Last Updated
July 2, 2017
Record last verified: 2010-06-17