NCT02091271

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
5,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Feb 2003

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

February 28, 2003

Completed
10.6 years until next milestone

First Submitted

Initial submission to the registry

September 20, 2013

Completed
6 months until next milestone

First Posted

Study publicly available on registry

March 19, 2014

Completed
6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 11, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 11, 2020

Completed
Last Updated

March 16, 2020

Status Verified

March 1, 2020

Enrollment Period

17 years

First QC Date

September 20, 2013

Last Update Submit

March 13, 2020

Conditions

Volunteers

Keywords

EvaluationResearchHealthy Volunteers

Outcome Measures

Primary Outcomes (2)

  • Develop a registry of individuals who meet eligibility criteria forexisting research projects

    ongoing

  • Evaluate volunteers/patients for participation in IRB approved clinicalstudies at NIA

    ongoing

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • All volunteers/patients who meet the criteria of an approved NIA protocol.
  • People with diagnosed or undiagnosed conditions
  • Patients may be eligible if they have rare, unusual, interesting or unknown conditions that require diagnosis

You may not qualify if:

  • Subjects unable to provide informed consent.
  • The volunteer/patient does not meet the criteria of any approved NIA protocol and does not wish to remain in the contact database for future studies.
  • Volunteer/patient has contacted the NIA Clinical Research Protocol Office and notified them that they would like to be removed and no longer contacted for NIA approved studies. They will be removed.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Institute of Aging, Clinical Research Unit

Baltimore, Maryland, 21224, United States

Location

Study Officials

  • Chee W Chia, M.D.

    National Institute on Aging (NIA)

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Time Perspective
OTHER
Sponsor Type
NIH
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 20, 2013

First Posted

March 19, 2014

Study Start

February 28, 2003

Primary Completion

March 11, 2020

Study Completion

March 11, 2020

Last Updated

March 16, 2020

Record last verified: 2020-03

Locations

US(1)