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Study for Intelligent Reminder System to Improve Pre-Exposure Prophylaxis Medication Adherence of MSM Population to Reduce New HIV Infection

Study on Intelligent Reminder System to Improve Pre-Exposure Prophylaxis Medication Adherence of MSM Population to Reduce New HIV Infection

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026414
Enrollment
Unknown
Registered
2019-10-08
Start date
2019-10-21
Completion date
Unknown
Last updated
2020-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

AIDS

Interventions

Blank control group:Routine interventions include free condom distribution, health education and regular HIV testing.
Routine intervention group:Oral Lamivudine tenofovir tablets 300mg and 300mg per day + electronic medicine box (bottle) compliance monitoring + routine interventions.
Intelligent medication reminder group:Routine intervention group + APPs intelligent reminder. APPs intelligent reminder system will include the following parts: 1. Compliance monitoring of electronic
3. Seve

Sponsors

Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
15 Years to 69 Years

Inclusion criteria

Inclusion criteria: 1. Men who have sex with men, aged 18-65 years; 2. HIV-uninfected. 3. An average of once or more sexual behavior a week. 4. There were at least three or more sexual partners a month before the trial. 5. The patient has signed the informed consent. 6. Willing to use experimental drugs under the guidance of follow-up arrangements; 7. Willing to participate in the experiment for 36 months.

Exclusion criteria

Exclusion criteria: 1. Those with a history of severe allergic diseases; 2. Patients with severe heart, liver (AST, ALT 1.5 times higher than the normal ceiling), or kidney (BUN, Cr over normal ceiling) or with hematopoietic disorder, hemorrhagic tendency, hemorrhagic diseases; 3. Patients with mental and neurological disorders; 4. Positive HBsAg or anti-HBc through screening; 5. Patients with advanced tumors; 6. Those with poor compliance and hard to complete the treatment; 7. Those whose life is in danger and can not complete the course of treatment; 8. Participated in clinical trials of new drugs or clinical trials of the same variety within 3 months. 9. Immune deficiency.

Design outcomes

Primary

MeasureTime frame
New HIV infection rate;

Countries

China

Contacts

Public ContactXiaoni Zhong

Chongqing Medical University

1932352920@qq.com+86 13308368059

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026