Screening Protocol to Evaluate Volunteers for NIA Approved Studies

Completed

• Conditions: Volunteers

• Registration Number: NCT02091271
• Lead Sponsor: National Institute on Aging (NIA)

Brief Summary

The National Institute on Aging (NIA) Intramural Research Program (IRP) has a number ofiRB approved research studies involving human subjects, both normal volunteers and patients. As a means of identifying interested volunteers and other participants in the research process, this screening mechanism is established to identif'y potential eligible participants for NlA protocols.

To participate, volunteers/patients must meet the specific requirements of at least one of the available NlA research studies; this protocol serves as a first step for admitting volunteers/patients to an appropriate approved protocol and creating a contact database for approved NlA studies.

This protocol will facilitate their recruitment into NIA approved studies and provide NlA staff the opportunity to examine subjects where diagnostic observations can be documented and evaluated for research potential.

Detailed Description

The screening protocol is designed to evaluate volunteers/patients for participation in IRB approved clinical studies of the National Institute on Aging (NIA). An additional purpose of this protocol is to develop a registry of individuals who have been evaluated through the NIA Clinical Research Unit screening clinic. To participate, volunteers/patients must meet the specific requirements of at least one of the available NIA research studies. This protocol serves as a first step for admitting volunteers/patients to an appropriate approved protocol, and it is used to develop a registry of individuals who meet eligibility criteria for existing research projects.

Study Timeline

• Study Start: 2003-02-28
• Study First Submitted: 2013-09-20
• Study First Submitted QC: 2014-03-14
• Study First Posted: 2014-03-19
• Status Verified: 2020-03
• Primary Completion: 2020-03-11
• Study Completion: 2020-03-11
• Last Update Submitted: 2020-03-13
• Last Update Posted: 2020-03-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 5000

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Evaluate volunteers/patients for participation in IRB approved clinicalstudies at NIA	ongoing
Develop a registry of individuals who meet eligibility criteria forexisting research projects	ongoing

Trial Locations

Locations (1)

National Institute of Aging, Clinical Research Unit; 🇺🇸 Baltimore, Maryland, United States