Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
All Genders
NCT05830305

MOBILE Health Intervention in IntraCerebral Hemorrhage Survivors

Led by The University of Hong Kong · Updated on 2026-01-06

140

Participants Needed

1

Research Sites

182 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized controlled trial investigates the efficacy and safety of mobile health intervention in managing hypertension after Intracerebral Hemorrhage (ICH).

CONDITIONS

Official Title

MOBILE Health Intervention in IntraCerebral Hemorrhage Survivors

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Primary Intracerebral Hemorrhage (ICH) diagnosis
  • Age 18 years or older
  • Discharge Modified Rankin Scale score of 4 or less
Not Eligible

You will not qualify if you...

  • Expected life expectancy less than 1 year
  • No access to the WeRISE app for patient or caregiver
  • Patient or caregiver unable to use the WeRISE app
  • Unable to perform home blood pressure monitoring
  • Unable to participate in follow-up activities
  • Contraindications for intensive and rapid blood pressure lowering, such as more than 70% cerebral vascular stenosis, history of falls, dizziness, or syncope from low blood pressure, or other medical conditions deemed unsuitable for low blood pressure
  • Bleeding tendency (platelet count less than 75 x 10^9/L or known coagulation disorders)
  • Severe kidney impairment (estimated glomerular filtration rate less than 30 ml/min/1.73m2)
  • Severe liver impairment (Child-Pugh C cirrhosis)
  • Known allergy or contraindication to two or more classes of anti-hypertensive drugs

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Queen Mary Hospital

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

K

Kay Cheong Teo, MBBS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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