NCT06524180

Brief Summary

The goal of this clinical trial is to evaluate whether patients assigned to the telemedicine (HealthCap) group demonstrate non-inferior blood pressure (BP) control compared to patients in the usual care group at 12 months. The main question it aims to answer is:

  • Do participants in telemedicine group have non-inferior daytime ambulatory blood pressure readings at 12-month, compared to usual care group?
  • Do participants in telemedicine group have better HT treatment, higher self-efficacy, reduced number of visits to primary care clinics and similar health care utilisation other than GOPCs, compared to usual care group? Participant in telemedicine group will:
  • Receive reminders to measure 7-day home blood pressure before their index consultation.
  • Get their drug refilled automatically as well as have consultations deferred 16-18 weeks later, if their blood pressure is under optimal control.
  • Have consultations as scheduled, if their BP is suboptimal or any of the safety questions screen positive. Participants in control group will:
  • Have consultation with physicians every 16-18 weeks.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
364

participants targeted

Target at P75+ for not_applicable hypertension

Timeline
17mo left

Started Oct 2024

Typical duration for not_applicable hypertension

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress53%
Oct 2024Sep 2027

First Submitted

Initial submission to the registry

July 16, 2024

Completed
13 days until next milestone

First Posted

Study publicly available on registry

July 29, 2024

Completed
2 months until next milestone

Study Start

First participant enrolled

October 1, 2024

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2027

Last Updated

December 10, 2025

Status Verified

December 1, 2025

Enrollment Period

3 years

First QC Date

July 16, 2024

Last Update Submit

December 8, 2025

Conditions

Keywords

blood pressuretelemedicinehome blood pressure measurement

Outcome Measures

Primary Outcomes (1)

  • daytime systolic blood pressure

    WatchBP O3 (Microlife AG, Switerzland) has been validated by multiple HT societies (www.stridebp.org) and will be used in the current RCT. BP will be measured every 30 min for ≥24 h, and patients' sleep diary will define the sleep duration. The readings will be considered valid if there are \>70% of valid readings overall, \>20 valid awake, and \>7 valid asleep BP readings in 24-h intervals.

    from the enrollment at 12-months

Secondary Outcomes (24)

  • Ambulatory blood pressure readings

    from enrollment at 6-month

  • Ambulatory blood pressure readings

    from enrollment at 12-month

  • Treatment adherence

    from enrollment at 6-month and 12-month

  • Self-efficacy

    from enrollment at 6 month and 12 month

  • Satisfaction with HealthCap

    from enrollment at 12 month

  • +19 more secondary outcomes

Study Arms (2)

Telemedicine

EXPERIMENTAL

Patients will be (i) given a validated HBPM device (ORMON HEM-7120) with appropriate cuff size, (ii) taught the HBPM technique, and (iii) taught to record HBPM readings using the HealthCap mobile app on their smartphones. Participants randomized to intervention will be reminded to take dual BP readings in the morning and evening for 1-2 weeks before the index consultation. These BP readings will be automatically sent to a computer at the clinic. When the HBPM mean is optimal (i.e., \<135/85 mmHg or \<130/80 mmHg \[for patients with cardiovascular diseases, renal diseases, and DM\]), other parameters will be checked using an online questionnaire. If no complaints are identified, the patient will have automatic drug refill and the physician appointment will be deferred for 16-18 weeks.

Device: Telemedicine

Usual care

ACTIVE COMPARATOR

Participants will continue receiving routine care, including anti-HT drug prescriptions, from their regular clinicians. In HK, patients with well-controlled HT are routinely seen every 16-18 weeks. Participants will also be given the same HBPM devices and taught the techniques. This is necessary because HBPM is a secondary outcome. According to the HK guidelines, all patients with HT are advised to regularly monitor their home BP, which can be considered as usual care.14 However, the patients will not be taught any BP measurement algorithm (such as that used in the telemedicine group). They will also be asked not to download or use any new HT mobile apps during the study period. In HK, all citizens have unlimited access to GOPCs and emergency departments for health problems. All participants are advised to seek medical help if BP becomes dangerously and persistently high (i.e. SBP ≥180 or DBP ≥110mmHg) or in case of any suspected medical emergencies.

Other: Usual care

Interventions

a mobile app and telemedicine platform to confirm good blood pressure control and may save doctor face-to-face consultation

Telemedicine

Participants will be followed up as usual by face-to-face consultation with the doctors

Usual care

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • (i) having a diagnosis of essential HT;
  • (ii) on anti-HT medications;
  • (iii) well-controlled HT on out-of-office BP measurements, including HBPM or ambulatory blood pressure measurements (ABPM) (measurement algorithm and details under methods). ABPM or HBPM are preferred to office BP due to their superior reproducibility and predictivity to cardiovascular outcomes. Furthermore, office BP misclassifies 30-40% of patients as having suboptimal BP control due to white-coat effect. From our pilot study, some patients with optimal BP are reluctant to undergo ABPM before recruitment into the RCT, and HBPM is more acceptable to these patients and is therefore included. According to local and international guidelines, optimal out-of-office daytime BP should be \&lt;135/85 mmHg for patients without comorbidities and \&lt;130/85 mmHg for patients with comorbidities that increase cardiovascular risk (i.e. stroke, ischaemic heart diseases, heart failure, diabetes mellitus (DM), and chronic kidney diseases) respectively;
  • (iv) can read basic Chinese (language used in the HealthCap);
  • (v) have used any mobile app (not HT-related) in the previous 1 year; and
  • (vii) aged between 18-80.

You may not qualify if:

  • (i) cannot provide informed consent;
  • (ii) unwillingness to conduct HBPM or repeated ABPM;
  • (iii) relative contraindications to ABPM (i.e., diagnosed atrial fibrillation, nighttime workers, occupational drivers, or patients with bleeding tendencies);
  • (iv) have severe mental illnesses that impair their ability to use HealthCap, including those diagnosed with schizophrenia, dementia, or as being actively suicidal;
  • (v) a diagnosis of other acute or chronic diseases that need regular physical assessments and/or medication changes (e.g., suboptimally controlled DM \[e.g., glycosylated haemoglobin (HbA1c)≥7%\], depression requiring medications, active cancer); and (vi) predicted lifespan of \&lt;1 year.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

HKW and NTEC GOPC

Hong Kong, Hong Kong, Hong Kong

RECRUITING

Related Publications (1)

  • Ng SN, Yip BH, Wang S, Leung M, Choi SYK, Leung SY, Han JJ, Tsui WW, Lai SY, Chan L, Mihailidou AS, McManus RJ, Sy J, Lee EK. Can TElemedicine system replace doctor consultations to Achieve non-inferior blood pressure in patients with Controlled Hypertension (TEACH)? Study protocol for a randomised controlled trial. Trials. 2025 Dec 8;27(1):31. doi: 10.1186/s13063-025-09350-3.

MeSH Terms

Conditions

Hypertension

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular Diseases

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical associate professor

Study Record Dates

First Submitted

July 16, 2024

First Posted

July 29, 2024

Study Start

October 1, 2024

Primary Completion (Estimated)

September 30, 2027

Study Completion (Estimated)

September 30, 2027

Last Updated

December 10, 2025

Record last verified: 2025-12

Locations