Can a single platform predict your risk for multiple chronic diseases?
NCT ID NCT07727915
First seen Jul 27, 2026 · Last updated Jul 28, 2026 · Updated 1 time
Summary
This pilot study is testing whether the ADEN platform can accurately identify people at risk for heart disease, respiratory problems, cancer, autoimmune conditions, and frailty. Researchers will compare the platform's risk ratings to those made by doctors. If it works, the platform could become a tool for early detection and prevention.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, the ADEN platform could provide a non-invasive way to detect early risk for multiple chronic diseases, enabling earlier interventions.
- What could go wrong
- This is a small pilot study (120 participants) focused on agreement with clinical assessment, not on health outcomes. The platform may not generalize beyond the Colombian population or meet the predefined success threshold.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2026
An estimate. End dates often move.
- Lead sponsor
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A research network
The lead sponsor is a research network or cooperative group.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
General population that meets the conditions of the different subgroups
- Ages
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18 to 99 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
8.2 General Inclusion Criteria * Age ≥ 18 years. * Capacity to provide valid informed consent. * Availability to attend a baseline medical evaluation. * Acceptance of the clinical and analytical use of collected information, under confidentiality and data protection regulations (Law 1581/2012). * Meeting at least one specific criterion of the assigned subgroup. 8.3 Exclusion Criteria * Active acute illness (infectious, inflammatory, or chronic disease exacerbation) within the past 4 weeks. * Patients undergoing intensive active oncological treatment (chemotherapy, ongoing radiotherapy) at the time of recruitment. * Severe decompensation of autoimmune, respiratory, or metabolic disease. * Serious uncontrolled systemic disease limiting participation (advanced organ failure, terminal-stage neoplasm). * Confirmed or suspected pregnancy. * Severe cognitive or psychiatric disorder without a responsible caregiver for consent and follow-up. * Insufficient clinical information or inability to complete minimum protocol measurements. * Simultaneous participation in another clinical study that could interfere with result interpretation. * Refusal to participate or absence of informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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UNIGEM
Medellín, Antioquia, 050021, Colombia
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