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Hypertension,EssentialENHANCeNCT07399912

Engaging Home-monitored Assessment to Navigate Clinical Decision-making

A study testing ENHANCe app and Teaching and training in people with Hypertension,Essential, run by SingHealth Polyclinics at 1 site in Singapore.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

This study is testing a new app called ENHANCe, which is designed to help family doctors manage patients with high blood pressure using readings taken at home. Read more about this study

Who is it for?
Ages 21 years and older
Conditions the study is for
Hypertension,Essential
What is being tested?
ENHANCe app and Teaching and training
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
116 participants
Where
1 siteSingapore
Study dates
1 Oct 2025to 1 Oct 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • For primary care physicians:
  • PCPs aged 21 years and above.
  • Involved in the clinical management of patients with hypertension in the past six months.
  • For patients:
  • Patients aged 21 years and above
  • Documentation of hypertension diagnosis in EMR
  • Owns an HBP monitoring device

Who cannot join

  • Documentation of dementia diagnosis in EMR
  • Audio or visual impairments
  • Hypertensive urgency or emergency

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Singapore1 site
  • SingHealth Polyclinics

    Singapore, Singapore, 150167

Other trials in Singapore

About this study

Official title: Engaging Home-monitored Assessment to Navigate Clinical Decision-making -The ENHANCe Study

This study is testing a new app called ENHANCe, which is designed to help family doctors manage patients with high blood pressure using readings taken at home.

Read the detailed description

The researchers want to find out if the app is easy to use in everyday clinic settings, whether doctors find it helpful and are willing to use it, and if it helps improve care. The study will involve 16 doctors and 100 patients with high blood pressure, split into two groups at two clinics. One group will use the ENHANCe app, which can read blood pressure data from different sources-including handwritten notes-and give doctors advice based on that information. The other group will receive regular care without the app. Over six months, researchers will collect feedback from doctors through surveys and group discussions at the end of the study. They'll also track how many people complete the study, how long clinic visits take, whether doctors follow the app's advice, and how well patients' blood pressure is controlled. The goal is to see if the app can help doctors make faster, better decisions and improve health outcomes for people managing their blood pressure at home.

Being tested
ENHANCe app, Teaching and training, Usual care
Keywords
Hypertension, Home blood pressure, Primary Care, Clinical decision support system
Medical subject headings
Essential Hypertension, Hypertension

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ENHANCe appDevice

    ENHANCe app is a prototype; it is a smartphone based clinical decision support (CDS) tool to manage patients with hypertension using their home blood pressure. The app will scan patients' home BP records from paper or mobile phone, and provide a recommendation to the doctor on how to manage their blood pressure. The patient will not need to use the device during the study period. However, the recommendation from the ENHANCe app will be available to the doctor to manage your blood pressure during the study period if the patient is in the intervention group.

  • Teaching and trainingOther

    All patients will have access to online educational resources throughout the study. After recruitment, they will receive a nurse-led education on HBP monitoring. The research team will train all primary care physicians (PCPs) on managing patients with hypertension using HBP records.

  • Usual careOther

    Physicians manage patients using HBP records at their discretion

Study groups in NCT07399912
Study groupRoleWhat they receive
Hypertension management using the Clinical Decision Support SystemExperimentalAll patients will have access to online educational resources throughout the study. After recruitment, they will receive a nurse-led education on HBP monitoring. The research team will train all primary care physicians (PCPs) on managing patients with hypertension using HBP records. The PCPs in the intervention group will be briefed on how the ENHANCe app works, and its recommendations. The ENHANCe app will be installed on designated mobile phones, and research staff will analyse HBP records during visits, documenting the output for PCPs to use. Based on the app's recommendations, patients will consult with intervention group PCPs 2-3 times throughout the study, with the last follow-up at 6 months. PCPs will complete a consult checklist after each visit. FGDs will be conducted with PCPs at the end of the study. The interviews will be recorded and transcribed for analysis.
Receives: Device: ENHANCe app; Other: Teaching and training
Hypertension management as per usual care without a clinical decision support systemOtherAll patients will have access to online educational resources throughout the study. After recruitment, they will receive a nurse-led education on HBP monitoring. The research team will train all primary care physicians (PCPs) on managing patients with hypertension using HBP records. Control group PCPs will manage patients using HBP records at their discretion, with a final follow-up scheduled at 6 months. PCPs will complete a consult checklist after each visit. Research staff will use the ENHANCe app to analyse BP diaries and document outcomes, but control group PCPs will not have access to the app or its results.
Receives: Other: Teaching and training; Other: Usual care

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Response rate of participants

    Participants agreeable to participate in the study

    Measured: 6 months

  2. Agreement with the CDSS recommendation among PCPs

    Proportion of PCPs who agree with the CDSS recommendation in the two groups

    Measured: 6 months

  3. Withdrawal rate

    Proportion of participants who withdrew

    Measured: 6 months

  4. Study completion rate

    Proportion of participants who completed the intervention

    Measured: 6 months

  5. Adverse event rates

    Proportion of adverse events reported in the two groups

    Measured: 6 months

  6. Consult duration

    Consult time in the groups

    Measured: 6 months

  7. Ease of home blood pressure record assessment among PCPS

    Ease of home blood pressure record assessment among PCPS in the two arms

    Measured: 6 months

Secondary outcomes (2)
  1. Proportion of CDSS recommendation followed by the PCPS

    Proportion of ENHANCe recommendations followed by the PCPs among the two groups

    Measured: 6 months

  2. Blood pressure control status

    Blood pressure control status among patients in the two groups

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Feb 2026
  2. Study start1 Oct 2025
  3. Primary completion1 Oct 2026 (estimated)
  4. Study completion1 Oct 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Model description
Parallel Cluster RCT
Masking
Single blind
Who is masked
Participant
Enrolment
116 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07399912
Sponsor's protocol ID
2024-4269-APP1
Acronym
ENHANCe
Status last verified
Sep 2025
First submitted
28 Dec 2025
Last updated
10 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: IPD will not be shared

Questions about this trial

What is this clinical trial studying?

A study testing ENHANCe app and Teaching and training in people with Hypertension,Essential, run by SingHealth Polyclinics at 1 site in Singapore.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 10 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Singapore. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Response rate of participants (time frame: 6 months). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Feb 2026.

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