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Engaging Home-monitored Assessment to Navigate Clinical Decision-making

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

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07399912
Acronym
ENHANCe
Enrollment
116
Registered
2026-02-10
Start date
2025-10-01
Completion date
2026-10-01
Last updated
2026-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension,Essential

Keywords

Hypertension, Home blood pressure, Primary Care, Clinical decision support system

Brief 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.

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.

Interventions

DEVICEENHANCe app

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.

OTHERTeaching and training

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.

OTHERUsual care

Physicians manage patients using HBP records at their discretion

Sponsors

SingHealth Polyclinics
Lead SponsorOTHER
Nanyang Polytechnic
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Masking description

Patient Participants will be blinded to the group they are allocated to

Intervention model description

Parallel Cluster RCT

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

for patients: * Documentation of dementia diagnosis in EMR * Audio or visual impairments * Hypertensive urgency or emergency

Design outcomes

Primary

MeasureTime frameDescription
Response rate of participants6 monthsParticipants agreeable to participate in the study
Agreement with the CDSS recommendation among PCPs6 monthsProportion of PCPs who agree with the CDSS recommendation in the two groups
Withdrawal rate6 monthsProportion of participants who withdrew
Study completion rate6 monthsProportion of participants who completed the intervention
Adverse event rates6 monthsProportion of adverse events reported in the two groups
Consult duration6 monthsConsult time in the groups
Ease of home blood pressure record assessment among PCPS6 monthsEase of home blood pressure record assessment among PCPS in the two arms

Secondary

MeasureTime frameDescription
Proportion of CDSS recommendation followed by the PCPS6 monthsProportion of ENHANCe recommendations followed by the PCPs among the two groups
Blood pressure control status6 monthsBlood pressure control status among patients in the two groups

Countries

Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026