Can a smartphone app help lower bad cholesterol?
NCT ID NCT05988866
First seen Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time
Summary
This trial investigates whether a digital health app called Lipodia can help lower LDL (bad) cholesterol in adults with high cholesterol. Participants either use the app alongside their usual treatment or continue with usual treatment alone. The study measures cholesterol levels and other health outcomes over six months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Lipodia digital health application
- What this could lead to
- If effective, Lipodia could offer a scalable, low-cost way to help people manage high cholesterol and reduce cardiovascular risk.
- What could go wrong
- This is a behavioral intervention, so results depend on user engagement. It may not work for everyone, and the study is relatively small (278 participants).
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.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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278 people
The number who actually took part.
- Started
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Feb 2025
- Finished
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May 2026
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- 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.
Inclusion criteria * Age ≥ 18 * Diagnosis of hypercholesterolemia (ICD-10 E78.0, E78.2, E78.4, E78.5, E78.8, E78.9) confirmed by a laboratory test and physician diagnosis * LDL-C levels above risk-adapted target * TG levels \< 400 mg/dL * Stability of potential drug treatment during the last 4 weeks * Stability of potential hormonal treatment during the last 6 months * Patient was made aware of lifestyle measures by GP or specialist * Consent to participation * Sufficient knowledge of the German language Exclusion criteria * Homozygous Familial Hypercholesterolemia (FH), given that it is a genetic condition which is relatively unresponsive to lifestyle changes * Hyperlipidemia type III, given that it is a genetic condition which is relatively unresponsive to lifestyle changes * Patients receiving plasmapheresis * Lp(a) \> 50 mg/dL * current pregnancy or planned pregnancy during the study period * planned major operations * liver dysfunction * end-stage renal failure * other systemic conditions that might interfere with successful study participation * Plans to change drug (including hormonal) treatment in the upcoming 6 months * Use of another digital intervention for hypercholesterolemia/dyslipidemia in the past
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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.
Contacts and locations
Locations
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GAIA AG
Hamburg, 22085, Germany
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