MOBILE-ICH: MOBILE Health Intervention in IntraCerebral Hemorrhage Survivors

Sponsor
The University of Hong Kong (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05830305
Collaborator
(none)
140
2
35

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Other: Mobile health intervention
N/A

Detailed Description

140 ICH survivors will be randomized into mobile health intervention (MOBILE) and the usual care group for hypertension management. All subjects will be educated on the importance of hypertension control after ICH and given lifestyle advice, including the DASH diet. Subjects in the MOBILE group will enter their home blood pressure (BP) measurements into a mobile stroke App (WeRISE) daily, and the study team will regularly review the BP measurements through a backend system. A protocol-based intervention via phone calls, which includes anti-hypertensive drug adjustment and reinforcement of lifestyle modification, will be implemented. Subjects in the usual care group will have their hypertension managed by their respective treating physicians. All subjects will be followed up for 26 weeks. The primary and secondary endpoints include the rate of controlled hypertension at 12 and 26 weeks.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
140 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
MOBILE Health Intervention in IntraCerebral Hemorrhage Survivors
Anticipated Study Start Date :
May 1, 2023
Anticipated Primary Completion Date :
Mar 31, 2025
Anticipated Study Completion Date :
Mar 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Mobile health intervention

Subjects will enter their home BP measurements into a mobile stroke App (WeRISE) daily, and the study team will regularly review the BP measurements through a backend system. A protocol-based intervention via phone calls, which includes anti-hypertensive drug adjustment and reinforcement of lifestyle modification, will be implemented.

Other: Mobile health intervention
A protocol-based intervention via phone calls, which includes anti-hypertensive drug adjustment and reinforcement of lifestyle modification, will be implemented.

No Intervention: Usual care

Subjects will have their hypertension managed by their respective treating physicians.

Outcome Measures

Primary Outcome Measures

  1. Rate of controlled hypertension 12 weeks after ICH [12 weeks]

    Office BP <130/80 mmHg

Secondary Outcome Measures

  1. Change of BP from recruitment to 12 weeks [12 weeks]

    The difference between BP measurement on recruitment and at 12 weeks

  2. Rate of controlled hypertension 26 weeks after ICH [26 weeks]

    Office BP <130/80 mmHg

  3. Morisky Medication Adherence Scale at 12 and 26 weeks [12 and 26 weeks]

    Score ranging from 0-8 points, with the higher scores indicating better drug adherence.

  4. Dietary Approaches to Stop Hypertension (DASH) diet Adherence Score at 12 and 26 weeks [12 and 26 weeks]

    Score ranging from 0-10 points, with the higher scores indicating better DASH diet adherence.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 85 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Primary ICH Diagnosis

  • Age ≥ 18 years

  • Discharge Modified Rankin Scale of ≤4

Exclusion Criteria:
  • Expected life expectancy of <1 year

  • Patient or caregiver does not have access to WeRISE App.

  • Patient or caregiver does not know how to use WeRISE App .

  • Inability to perform home BP monitoring

  • Inability to participate in follow-up activity

  • Contraindication for intensive and rapid lowering of blood pressure (Known >70% cerebral vascular stenosis; History of fall, dizziness or syncope due to hypotension; Any other medical condition that is deemed contraindicated for low blood pressure

  • Bleeding tendency (Platelet count < 75 x 10^9/L; Known coagulation disorder)

  • Severe renal impairment (Estimated glomerular filtration rate using CKD-EPI formula <30 ml/min/1.73m2)

  • Severe liver impairment (Child-Pugh C cirrhosis)

  • Known contraindication or allergy to two or more anti-hypertensive classes

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • The University of Hong Kong

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Teo Kay-Cheong, Honorary Clinical Assistant Professor, The University of Hong Kong
ClinicalTrials.gov Identifier:
NCT05830305
Other Study ID Numbers:
  • UW 22-702
First Posted:
Apr 26, 2023
Last Update Posted:
Apr 26, 2023
Last Verified:
Apr 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 26, 2023