Heart age app trial tests digital nudge against cardiovascular disease
NCT ID NCT05827861
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed trial in Singapore tested whether telling people their 'heart age' and giving them a behavior-change app (HOPE-CVD) could lower their risk of heart disease. Over 1,100 adults aged 30-74 with at least a 5% risk were split into four groups, each receiving different levels of risk information and app support. The study measured changes in predicted heart risk, blood pressure, cholesterol, and healthy behaviors after 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
- HeartAge risk presentation and HOPE-CVD mobile app (behavioral interventions)
- What this could lead to
- If successful, this approach could provide a simple, scalable way to help people lower their heart disease risk using personalized risk communication and digital behavior support.
- What could go wrong
- The trial is completed but results are not yet published, so we don't know if it worked. It also excluded people needing medication, so findings may not apply to higher-risk groups.
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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1,121 people
The number who actually took part.
- Started
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May 2023
- Finished
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Oct 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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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30 to 74 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: 1. Aged 30-74 years; 2. Singapore citizen, or permanent resident 3. Able to read and understand English 4. Have access to and is comfortable using an internet-enabled device 5. At least 5% risk of CVD, as measured by the Framingham Risk Score (FRS), based on previous health screening results Exclusion Criteria: 1. Existing heart disease or a prior history of coronary artery disease/angina/myocardial infarction/revascularisation, transient ischaemic attack/stroke, peripheral vascular disease, heart failure and cardiac arrhythmia 2. Suffering from cancer or chronic kidney disease 3. Currently prescribed with statins, exetimibe and pcsk-9 inhibitors to treat cholesterol levels 4. Been told by a doctor that they should only do physical activity recommended by a doctor due to a heart condition 5. Serious mental illness (Eg. A patient who is suffering from serious mental illness refers to those who need assistance in daily activities due to their mental illness.) 6. The following groups of individuals will be excluded as most of them would require pharmacological therapy for risk factors based on clinical guidelines in Singapore: * Diagnosed with diabetes * For those with FRS of 5-9%, LDL ≥160mg/dL * For those with FRS of 10-19%, LDL ≥130mg/dL * For those with FRS of ≥20%, LDL ≥100mg/dL * Total cholesterol \>280 mg/dL at the point of screening * Systolic blood pressure \>160 mmHg at the point of screening * Triglycerides ≥4.5 mmol/L 7. Pregnant or planning to be pregnant in the next 7 months 8. Unable to give informed consent 9. Current or previous participants in HOPE Pilot Study, or HOPE-CVD-GP study 10. Members of the same household or family of existing enrolled participants
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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
-
National University of Singapore
Singapore, Singapore, 117549, Singapore
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Other studies related to the condition(s) this trial covers.
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