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NCT07128966Recruiting

Direct to Patient Minimal Risk Biospecimen and Data Collection Research

Joined Bio - JB-MR-250225, Direct to Patient Minimal Risk Research

Source: ClinicalTrials.gov · Last updated 5 May 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
100000 (estimated)
First submitted
11 Aug 2025
Start date
1 Apr 2025
Primary completion date
1 Sept 2035
Lead sponsor
Joined Bio
NCT number
NCT07128966

What you commit to

  • Study type: Observational
  • Planned participants: 100000
  • From 1 Apr 2025 to the primary completion date, 1 Sept 2035
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • 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.

Who the study is looking for

  • 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.

Age in the registry: 18 years to 90 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Joined Bio
Coordinator of this site? Confirm its status
LexingtonUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.