Evaluating a tailored healthcare delivery model for people living with HIV and other health conditions

Is this trial a fit for you?

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

What this trial studies

This implementation study assesses a differentiated service delivery model aimed at improving care for people living with HIV (PLWH) who also have chronic comorbidities. Utilizing a Hybrid Type 3 study design, the research focuses on evaluating implementation outcomes and client service outcomes through the RE-AIM framework. Participants will be recruited from an HIV clinic in Hong Kong, where they will complete a survey to express their willingness to participate. The study aims to address the challenges of managing comorbidities in PLWH by exploring innovative healthcare delivery methods.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* PLWH eligible to participate in this study are PLWH aged 18 years or above
* followed up at the HIV Clinic, and with one or more cardiometabolic comorbidities, including hypertension, diabetes, hyperlipidaemia, metabolic-associated fatty liver disease, cardiovascular diseases, and cerebrovascular diseases. They will be eligible if HIV physicians consider them having sub-optimal control of their comorbidities, suspected of having complications, or would benefit from screening of complications resulting from their comorbidities. These indications are selected as they involve specialist care, including investigations and treatment, which are not available at the HIV Clinic.

Exclusion Criteria:

* Incompetent subjects who cannot give informed written consent.

Where it's running

• Prince of Wales Hospital
  Shatin, Hong Kong Recruiting

Study contacts

• Principal investigator: Grace LUI — Chinese University of Hong Kong
• Study coordinator: Grace LUI
• Email: gracelui@cuhk.edu.hk
• Phone: 35051716

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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.