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NCT07072689Recruiting

A Multi-centre Study Evaluating the Performance and Acceptance of the Hilo Band Cuffless Blood Pressure Medical Device in the Normo-, Hypo- and Hyper-tensive Young Population: a Comparison With the 24-h Ambulatory Blood Pressure Monitoring (ABPM)

Source: ClinicalTrials.gov · Last updated 13 Oct 2026

Brief summary (registry, in English)

Hypertension is one of the main risk factors for the onset of cardiovascular diseases. It is often silent, and most individuals are unaware they have it. The 24-hour Ambulatory Blood Pressure Monitoring (24-hour ABPM) device allows for continuous blood pressure (BP) monitoring over a 24-hour period and is currently considered the gold standard for diagnosing hypertension. However, it is expensive, time-consuming for healthcare personnel, bulky, and often uncomfortable to wear-especially during the night. Recently, other BP monitoring devices have entered the market. One of them is the Aktiia bracelet, renamed as Hilo band as of 8 april 2025, (Hilo band SA, Neuchâtel, Switzerland), CE-marked, which estimates BP and heart rate using a pulse wave analysis (PWA) technique. Hilo band is non-invasive, comfortable to wear, and allows for long-term BP monitoring. Especially in adolescents, BP monitoring might present a special challenge due to high physical activity and often low compliance. Wearable technologies like Hilo band could offer an interesting alternative to the traditional 24-h ABPM. Results in young active adults and adolescents might be different comparing between Hilo and the 24-h ABPM and need to be assessed. Furthermore, adolescents often dislike the 24-h ABPM beacuse of the discomfortable BP cuff (specially during the night) and the stigmatic effect of the 24-h ABPM at school/work. To conclude, there is a need especially in young people of comfortable, precise and user-friendly technique for long term BP measurement and monitoring. However, there is insufficient data to support the use of Hilo band in healthcare settings for the diagnosis and monitoring of hypertension. In one study, Hilo band was compared to the 24-hour ABPM only for daytime BP readings in a population enrolled in a cardiac rehabilitation program, and thus was not tested in apparently 'healthy' individuals who may be hypertensive. Another study assessed Hilo band's performance compared to double auscultation in older adults aged 65 to 85 years in different body positions (sitting, standing, and lying down); therefore the young population and adolescents were not considered. In our research project, we aim to evaluate the performance of Hilo band compared to 24-hour ABPM in a young population (including adolescents), considering both daytime and nighttime blood pressure measurements.

Status (registry)
Recruiting
Study type
Observational
Enrollment
60 (estimated)
First submitted
11 Jun 2025
Start date
1 Dec 2025
Primary completion date
1 Dec 2028
Lead sponsor
Simonetti Giacomo
NCT number
NCT07072689

What you commit to

  • Study type: Observational
  • Planned participants: 60
  • From 1 Dec 2025 to the primary completion date, 1 Dec 2028
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Allergies to silicone
  • Subjects with arrhythmia
  • Exfoliative skin diseases and lymphoedema or damaged/injured skin at the wrist
  • Individuals with lack of judgment/mental illness
  • Pica disorder

Lab values

  • Patients suffering from pathologies that systematically reduce peripheral perfusion including Raynaud's disease, diabetes, renal dysfunctions (eGFR \< 30mL / min / 1.73 m2), untreated hyper-/ hypothyroidism, pheochromocytoma, or arteriovenous fistula

Other

  • Atrial fibrillation
  • Interarm Systolic Blood Pressure (SBP) difference over 10% or Diastolic Blood Pressure (DBP) difference over 10%
  • Arm paralysis
  • Amputated upper limb
  • Arm trembling or shivering
  • Upper arm circumference \> 64 cm
  • Wrist circumference \> 22 cm
  • Pregnant women
  • Sleepwalking and severe insomnia

Who the study is looking for

  • Population 1:
  • Informed Consent signed by the subject/legal representative
  • 14-20 years of age
  • Clinical indication to receive a 24-h ABPM measurement
  • Functional internet phone connection
  • Negative pregnancy test, ongoing anti-conceptive treatment or declaration of the subject not being pregnant
    • Population 2:
  • Informed Consent signed by the subject
  • 21-35 years of age
  • Clinical indication for receiving a 24-hour blood pressure measurement
  • Functional internet phone connection
  • Negative pregnancy test, ongoing anti-conceptive treatment or declaration of the subject not being pregnant
    • Population 3
  • Informed Consent signed by the subject
  • 21-35 years of age
  • Functional internet phone connection
  • Negative pregnancy test, ongoing anti-conceptive treatment or declaration of the subject not being pregnant

Age in the registry: 14 years to 35 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ente Ospedaliero Cantonale
Coordinator of this site? Confirm its status
BellinzonaSwitzerlandRecruiting
Geneva University Hospitals-Hug
Coordinator of this site? Confirm its status
GenevaSwitzerlandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.