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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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16 December 2017 |
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Main ID: |
NCT03209024 |
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Date of registration:
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03/07/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Smartphone App Assisted Home Blood Pressure Monitoring Amongst Hypertensive Patients in Singapore
ADELPHY |
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Scientific title:
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App Documentation of Electronic BP Readings in Hypertension |
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Date of first enrolment:
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March 15, 2017 |
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Target sample size:
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80 |
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Recruitment status: |
Active, not recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT03209024 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Other. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Singapore
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Contacts
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Name:
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Tazeen Jafar, MD, MPH |
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Address:
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Telephone:
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Email:
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Affiliation:
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Duke-NUS Medical School |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Singaporean citizen or permanent resident
- Able to communicate in English
- Diagnosis of essential hypertension and on at least one antihypertensive medical
therapy
- Between 40-70 years of age
- Owns a smartphone compatible with the study
- Has been visiting the study polyclinic for at least 1 year
Exclusion Criteria:
- Known cardiac arrhythmia
- Known end stage renal disease
- Known cancer patient
- Known history of stroke
- Known history of myocardial infarct
- Physical or mental disability that would prevent one's own measurement of home BP
(e.g. visual impairment, dementia)
- Maximal arm circumference exceeding BP cuff size
- Anticipation of extensive travel overseas during study period
- Occupation requires night shift
- Participating in other clinical trials
Age minimum:
40 Years
Age maximum:
70 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Hypertension
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Intervention(s)
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Device: Smartphone assisted wireless recording of home blood pressure readings
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Other: Handwritten logbook recording of home blood pressure readings
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Primary Outcome(s)
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Home Blood Pressure Recording Fidelity within each study arm
[Time Frame: Baseline visit to 3 weeks post randomization]
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Secondary Outcome(s)
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The association of participants' years of smartphone use with home blood pressure recording fidelity within each study arm
[Time Frame: Baseline visit to 3 weeks post randomization]
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The association of participants' highest level of education with home blood pressure recording fidelity within each study arm
[Time Frame: Baseline visit to 3 weeks post randomization]
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The association of participants' age with home blood pressure recording fidelity within each study arm
[Time Frame: Baseline visit to 3 weeks post randomization]
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Secondary ID(s)
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2017/2014
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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