Clinical Trials in Taiwan / NCT06183723
Enrolling by invitation Not applicable

Optimizing Care for Challenging People Living With HIV

NCT06183723 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2024-03-18
Last updated
2025-09-08

Condition(s) studied

Adherence, MedicationHIV InfectionsSocial Media

Investigational drug(s) / intervention(s)

Combination of social-behavior model and eHealth

Combination of social-behavior model and eHealth: The study examines how an intervention combining the social-behavior model and eHealth can improve medication adherence among individuals who struggle to follow their medical regimens. The platform offers multiple features including health education, medication reminders, online consultations, chat rooms, news, and Q\&A services. The intervention and follow-up are based on a 28-day month. The first intervention period runs from the first to the third month post-enrollment, with the introduction of the main features and sharing of health education videos and monthly short films. A follow-up assessment and questionnaire are completed after the third month. The second intervention period is between the fourth and sixth months and includes similar features, and face-to-face counseling. New health education videos and monthly short films are shared as well. After the sixth month, another assessment is conducted to evaluate the post-intervention effects.

Study summary

Conduct an intervention combining social and behavioral health models with digital health technologies to improve their adherence to their medication schedules. The success of the intervention is assessed by comparing adherence rates before and after its implementation to see if there's a notable enhancement in how well patients follow their antiretroviral therapy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1\. PLWH with adherence below the specific proportion of days covered (PDC), which is defined as the specific level that corresponds to 90% at viral suppression (\< 200 copies/mL). Exclusion Criteria: 1. Under 18 years of age. 2. Illiterate. 3. Non-consenting individuals. 4. Less than 365 days from the initial use of antiretroviral drugs to the assessment for inclusion in the study. 5. Inability to obtain complete medication records for the 365 days prior to inclusion. 6. Lack of a smart phone. 7. No willingness to return for follow-up at the participating hospital.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kaohsiung Medical University Chung-Ho Memorial Hospital Kaohsiung City Taiwan

More Kaohsiung Medical University Chung-Ho Memorial Hospital trials in Taiwan

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06183723 on ClinicalTrials.gov ↗ ← All trials in Taiwan