Direct to Patient Minimal Risk Biospecimen and Data Collection Research
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorJoined Bio
About this trial
This study aims to help researchers better understand health conditions and develop improved tests, treatments, and cures for diseases. Joined Bio collects health data, lifestyle information, biological samples, and feedback from participants and provides this to qualified research partners.
Eligibility criteria
Qualifiers
Male or female, that are adults [have reached the Age of Majority = aged 18 to 90 in most US states; aged 19-90 in Alabama or Nebraska; aged 21-90 in Mississippi or Puerto Rico].
Have reviewed and signed a consent or e-consent form for this study. If a person with diminished decision-making capacity, their Legally Authorized Representative has reviewed and signed the consent for on their behalf.
Be willing to comply with all study procedures and be available for the duration of the study.
Meets requirements of a current request for research participation (e.g. has previous diagnosis of a medical condition of interest or laboratory results within a specific range).
Disqualifiers
Unable to meet the Inclusion Criteria listed above.
Prisoners or children
Unable to provide the requested biospecimen(s), data or feedback without placing the individual at risk.
Trial design
Treatments tested in this trial
- Observation
Treatment groups
100,000 Participants
are divided into 2 treatment groupsLocations
1Joined Bio02420, LexingtonMassachusetts, United States
Sponsors and collaborators
Joined Bio
Lead sponsor
Source ClinicalTrials.gov