UnknownNot Applicable

Instant Message-delivered Personalised Lifestyle Modification Intervention for Pre-hypertension Adults

Hong Kong256 participantsStarted 2024-05-01

Plain-language summary

To assess the effectiveness of instant message-delivered personalised lifestyle modification (LSM) intervention for pre-hypertension (pre-HTN) management among community dwelling Chinese adults.

Who can participate

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Systolic BP 120-139 or diastolic BP 80-89mmHg. The BP screening procedures and requirements (i.e., office BP measurement and ABPM) will strictly follow the International Society of Hypertension's Global Hypertension Practice Guidelines;
✓. Aged ≥18 years;
✓. Able to read and communicate in Chinese; and
✓. Able to use mobile phone instant messaging function.

Exclusion criteria

✕. Ever diagnosis of HTN;
✕. Ever diagnosis of cardiovascular diseases (CVDs);
✕. Pregnant or \<3-month post-partum;
✕. Current diagnosis of psychiatric disease or currently taking a psychotropic drug; and
✕. Currently participating in any type of BP reduction intervention.

What they're measuring

24hr-systolic and diastolic BP

Timeframe: 6 months

Trial details

NCT IDNCT06504849

SponsorThe University of Hong Kong

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-09

Contact for this trial

Jung Jae Lee

+852 3917 6971 leejay@hku.hk

View on ClinicalTrials.gov More Pre-hypertension trials