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- Klinische proef NCT00644150
Effectiveness of HIV/Sexually Transmitted Infection Training for Physicians in China
Project Ai Shi Zi: Integrating HIV/STI Prevention and Treatment in China
Studie Overzicht
Toestand
Conditie
Gedetailleerde beschrijving
HIV and sexually transmitted infections (STIs) are among the foremost public health concerns worldwide, with the number of infections continuing to rise significantly. Specifically, in China, the number of cases of HIV is estimated to rise from 650,000 in 2006 to more than 10 million by the year 2010. The reasons for the drastic increase may be associated with a lack of education about proper condom use and consequences of sexual risk behaviors and the existing stigma toward HIV/STI patients. Therefore, increased knowledge of HIV/STI prevention and treatment is necessary for both physicians and patients in China. A program that provides training in HIV/STI prevention, treatment, and management to physicians may be an effective means of enhancing their abilities to deliver high quality, integrated HIV/STI prevention and treatment. The Ai Shi Zi program, which provides training on stigma, risk-reduction counseling methods, and treatment skills to county and township level physicians in China, may be an effective means of implementing HIV/STI training. This study will evaluate the effectiveness of the Ai Shi Zi program in improving HIV/STI diagnosis, treatment, and management by Chinese physicians and in reducing the number of subsequent HIV/STI infections in their patients.
Participants in this study will include county level physicians and their patients and township level physicians. All physicians will first undergo baseline assessments that will include questions about knowledge of HIV/STI, capability of administering HIV/STI screening and risk-reduction counseling, and attitudes toward working with HIV/STI-infected individuals. Physicians will then be assigned randomly to receive the Ai Shi Zi program or no training.
Physician training in the Ai Shi Zi program will consist of multiple components: an orientation workshop on fundamental knowledge and skills of HIV/STI treatment and prevention, a 3-month practice period, a 3-month post-practice seminar on preventive counseling, another 3-month practice period, and a 6-month post-practice seminar on clinical HIV and STI management. Physicians will keep weekly journals during both 3-month practice periods, citing the most interesting or difficult STI or HIV case they experienced during the week. The practice periods will promote learning-by-doing to further enhance physicians' abilities to deliver high quality, integrated HIV/STI prevention and treatment. Both post-practice seminars will allow physicians to share experiences gained during the previous 3-month practice period. County level physicians will receive the seminar training from experts in the fields of HIV/STIs, behavioral counseling, and stigma reduction. After completing the first post-practice seminar, the county level physicians then, in turn, will present the training to the township level physicians. All physicians will undergo repeat baseline assessments at post-training; post-practice seminars; and Months 1, 2, and 15 after orientation.
Upon completion of the 6-month post-practice seminar, physicians will begin to implement the Ai Shi Zi program in their clinics. Each patient participant who seeks treatment from physician participants, who have received either Ai Shi Zi training or no training, will first undergo a test for chlamydia and gonorrhea. On this initial visit, the physicians who have received the Ai Shi Zi program will provide HIV/STI risk-behavior counseling to their patients. The counseling will include discussion of topics such as partner notification, HIV/STI prevention, expected difficulties in changing behaviors, and development of a risk-reduction plan. Patient participants will then return within 2 weeks to receive their test results and additional behavioral counseling. If the STI is confirmed by the lab test, patients will be treated with standard care and will be asked to complete an assessment. The assessment will include a 30-minute interview about HIV/STI-related knowledge, attitudes, beliefs, practices, service utilization, and risk behaviors. Nine months after baseline, patient participants will undergo a repeat interview.
Studietype
Inschrijving (Werkelijk)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
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Anhui
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Hefei, Anhui, China
- Anhui Medical University
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria for Patient Participants:
- Tests positive for the presence of gonorrhea or chlamydia
- Plans on living in current community for at least 9 months after study entry
- Willing to provide contact information for 9-month follow-up
Inclusion Criteria for County Level Physician Participants:
- Specializes in STI, obstetrics/gynecology, urology, infectious disease, or HIV care
- Minimum of 3 years of clinical experience as verified by practice supervisor
- Sees HIV/STI and related patients in his/her practice
- Willing to participate for the entire duration of the training, including secondary training stage
Inclusion Criteria for Township Level Physicians Participants:
- Minimum of 3 years of clinical experience as verified by practice supervisor
- Works in a high service volume area (among the top one-third within his/her host township health center)
- Sees HIV/STI and related patients in his/her practice
- Willing to participate for the entire duration of the training, including secondary training stage
Exclusion Criteria for All Participants:
- Presence of an obvious psychological/psychiatric disorder that would invalidate the informed consent process or otherwise contraindicate participation in the assessment
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Preventie
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
---|---|
Experimenteel: 1
Physicians of county level will receive Ai Shi Zi training provided by experts in the fields of HIV/STIs, behavioral counseling, and stigma reduction.
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This training uses a curriculum developed specifically for Project Ai Shi Zi and includes training in stigma; risk-reduction counseling; and quality HIV/STI diagnosis, treatment, and management.
Physician training will consist of multiple components: an orientation workshop on fundamental knowledge and skills of HIV/STI treatment and prevention, a 3-month practice period, a 3-month post-practice seminar on preventive counseling, another 3-month practice period, and a 6-month post-practice seminar on clinical HIV and STI management.
The practice periods will promote learning-by-doing to further enhance physicians' abilities to deliver high quality, integrated HIV/STI prevention and treatment.
Post-practice seminars will allow participants to share experiences gained during the previous 3-month practice period.
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Experimenteel: 2
Physicians of township level will receive Ai Shi Zhi training provided by the county level physicians.
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This training uses a curriculum developed specifically for Project Ai Shi Zi and includes training in stigma; risk-reduction counseling; and quality HIV/STI diagnosis, treatment, and management.
Physician training will consist of multiple components: an orientation workshop on fundamental knowledge and skills of HIV/STI treatment and prevention, a 3-month practice period, a 3-month post-practice seminar on preventive counseling, another 3-month practice period, and a 6-month post-practice seminar on clinical HIV and STI management.
The practice periods will promote learning-by-doing to further enhance physicians' abilities to deliver high quality, integrated HIV/STI prevention and treatment.
Post-practice seminars will allow participants to share experiences gained during the previous 3-month practice period.
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Experimenteel: 3
HIV/STI patients will receive standard of care and specialized care from physician participants trained in Ai Shi Zi.
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If an STI is confirmed by a lab test, participants will receive standard of care treatment.
Gonorrhea will be treated with a single dose of 250 mg of ceftriaxone sodium administered by intramuscular injection.
If patients are allergic to ceftriaxone, they will be treated with azithromycin (2 g single oral dose).
Chlamydia will be treated with azithromycin (1 g single oral dose).
On the initial visit, participants will receive HIV/STI risk-behavior counseling from the physician trained in Ai Shi Zi.
The process is based on motivational interviewing techniques and will include discussing topics such as partner notification, HIV/STI prevention, and expected difficulties in changing behaviors.
This risk-reduction model encourages the HIV/STI-infected or -uninfected person to develop a risk-reduction plan.
The objective is to decrease the chance of infection for that individual and for others, too.
Patients will develop a list of risk-reduction strategies to follow.
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Geen tussenkomst: 4
Physicians of county level who will not participate in Ai Shi Zi training
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Geen tussenkomst: 5
Physicians of township level who will not participate in Ai Shi Zi training
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Sham-vergelijker: 6
HIV/STI patients who will receive standard care only
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If an STI is confirmed by a lab test, participants will receive standard of care treatment.
Gonorrhea will be treated with a single dose of 250 mg of ceftriaxone sodium administered by intramuscular injection.
If patients are allergic to ceftriaxone, they will be treated with azithromycin (2 g single oral dose).
Chlamydia will be treated with azithromycin (1 g single oral dose).
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
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Scores from curriculum exams performed by physicians
Tijdsspanne: Measured at Month 15
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Measured at Month 15
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Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
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Incidence of STIs in intervention patients
Tijdsspanne: Measured at Month 9
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Measured at Month 9
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Medewerkers en onderzoekers
Medewerkers
Onderzoekers
- Hoofdonderzoeker: Thomas J. Coates, PhD, University of California, Los Angeles
Publicaties en nuttige links
Studie record data
Bestudeer belangrijke data
Studie start
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Schatting)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- R01MH075639 (Subsidie/contract van de Amerikaanse NIH)
- DAHBR 9A-ASG-P
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .
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