Direct to Patient Minimal Risk Biospecimen and Data Collection Research (NCT07128966) | Clinical Trial Compass
RecruitingNot Applicable
Direct to Patient Minimal Risk Biospecimen and Data Collection Research
United States100,000 participantsStarted 2025-04-01
Plain-language summary
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.
Who can participate
Age range18 Years – 90 Years
SexALL
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Inclusion Criteria:
* 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).
* Pregnant women may be enrolled in this study in accordance with 45 CFR Part 46 Subpart B.
Exclusion Criteria:
* 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.