NCT06082661

Brief Summary

The objective of this biospecimen collection protocol is the acquisition of blood from adult volunteers. These biospecimens will be transferred to the College of Medicine (COM)/Burnett School of Biomedical Sciences (BSBS) research scientists and their research teams for testing according to their separate IRB-approved/exempted protocols. These separate IRBapproved protocols cannot be for genetic testing.

Trial Health

77
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
13mo left

Started Jun 2022

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress78%
Jun 2022Jun 2027

Study Start

First participant enrolled

June 23, 2022

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

October 3, 2023

Completed
10 days until next milestone

First Posted

Study publicly available on registry

October 13, 2023

Completed
3.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2027

Last Updated

December 6, 2024

Status Verified

December 1, 2024

Enrollment Period

4.9 years

First QC Date

October 3, 2023

Last Update Submit

December 3, 2024

Conditions

Keywords

BloodHealthy

Outcome Measures

Primary Outcomes (1)

  • Acquisition of blood samples for testing

    This is a non-clinical, biospecimen collection study.

    5 years

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

This study does not specifically target a particular vulnerable population.

You may qualify if:

  • Male or female adults
  • years old or older
  • weigh over 110 pounds
  • able to provide informed consent

You may not qualify if:

  • pregnant/suspect to be pregnant
  • prisoners
  • have donated blood anywhere in the preceding 16 weeks

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Central Florida

Orlando, Florida, 32816, United States

RECRUITING

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 3, 2023

First Posted

October 13, 2023

Study Start

June 23, 2022

Primary Completion (Estimated)

June 1, 2027

Study Completion (Estimated)

June 1, 2027

Last Updated

December 6, 2024

Record last verified: 2024-12

Data Sharing

IPD Sharing
Will not share

Locations