Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Prevent non-communicable diseases by screening and helping emergency department patients adopt healthier lifestyles

Official title: A Proactive Approach to Prevent Non-communicable Diseases Through Screening and Educating Emergency Department Attendees to Adopt Healthy Lifestyles: A Randomised Clinical Trial

Run by Chinese University of Hong Kong · NCT06889792 · Data updated 2026-11-12

This program will test whether a brief screening, tailored advice, a resource leaflet, and a follow-up phone call can help adult ED patients with health-risk behaviors adopt healthier lifestyles.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment1172 (estimated)
SponsorChinese University of Hong Kong
Academic / other
Locations1 site (Hong Kong)
StatusRecruiting
StartedJune 10, 2025
Main results expectedJune 30, 2027
Study endsJanuary 31, 2028
Registry record updatedJanuary 29, 2026
Trial IDNCT06889792 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (≥18 years) who are Chinese, triaged as semi-urgent or non-urgent and discharged home from participating Hong Kong EDs, who report at least one health-risk behavior and own and can use a smartphone with messaging apps.

Probably not a fit

People already diagnosed with NCDs and receiving regular outpatient care, those with cognitive impairment or serious mental illness, or those without smartphone/messaging access are unlikely to benefit or be eligible.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an assessor-blinded, multicentre randomized controlled trial enrolling 1,172 adult attendees from five acute hospital emergency departments in Hong Kong. Participants complete a behavioral risk questionnaire and basic measures (blood pressure, BMI) and are randomized to receive brief health warning and tailored advice based on self-determination and the theory of planned behaviour plus a resource leaflet and follow-up booster calls, or to usual care. Quality of life will be measured with the EQ-5D-5L and outcomes will focus on changes in health-risk behaviors and related measures over follow-up. Behavioral techniques such as the foot-in-the-door method and follow-up boosters are used to encourage adoption of healthier habits.

Why it matters

Potential benefit: If successful, the program could reduce modifiable risk behaviors, lower future risk of non-communicable diseases, and improve participants' quality of life.

How similar studies have gone: Some ED-based brief interventions have shown modest success for single risks (e.g., alcohol, smoking), but multi-behavior interventions based on self-determination theory are less well established.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* being aged ≥18 years old Chinese
* being triaged as semi-urgent (level 4) or non-urgent (level 5) and discharged home on the same day after receiving medical attention
* having at least one health risk behaviour (tobacco use, harmful alcohol consumption, unhealthy diet, and physical inactivity)
* owning a smartphone and having an ability to use instant messaging applications (e.g. WhatsApp or WeChat).

Exclusion Criteria:

* having a poor cognitive state or mental illness
* being diagnosed with NCDs and undergoing regular follow-ups in outpatient clinics
* participating in another related study

Where it's running

  • The Nethersole School of Nursing, The Chinese University of Hong Kong
    Hong Kong, Hong Kong
    Recruiting

Study contacts

  • Principal investigator: Ho Cheung William Li, PhD — The Nethersole School of Nursing, CUHK
  • Study coordinator: Ho Cheung William Li, PhD
  • Email: williamli@cuhk.edu.hk
  • Phone: +85239430889

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.