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| ID | Type | Description | Link |
|---|---|---|---|
| 1U19AI051915-01 | U.S. NIH Grant/Contract | View source | |
| CIPRA CH 002 |
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| Name | Class |
|---|---|
| Comprehensive International Program of Research on AIDS | OTHER |
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The purpose of this study is to determine whether two educational programs about HIV will improve the quality of life of HIV infected people living in the rural villages of China. The study will enroll HIV infected adult residents, influential community members, and other community members of selected villages of Funan County or Yingzhou District, Anhui Province, China.
A previous study found that HIV-infected villagers in Anhui Province, China describe their quality of life as poor. While poverty, poor health, stigma, and discrimination contribute to this poor quality of life, all these issues are interrelated and deserve further investigation. The quality of life for HIV-infected people may be made better through education, either for HIV-infected people to learn more about HIV, the treatments they are receiving, and how to deal with their disease, or for HIV uninfected people to understand HIV infection and to reduce stigma and discrimination associated with HIV infection. This study will provide skills training to HIV-infected adults and anti-stigma and anti-discrimination training to influential community members. The purpose of this study is to evaluate the changes in quality of life in HIV-infected villagers living in Anhui Province, China that result after these two training programs are administered.
There will be 3 groups in this study. Group 1 participants will be HIV-infected villagers. Group 1 participants will take part in 2-hour skills training sessions every week from study entry to Week 8. Participants will also be asked to bring a family member to each training session. After completing training, participants will be asked to complete a post-training evaluation of the training sessions. Group 1 participants will be asked to complete questionnaires at study entry and 6 and 12 months after completion of training.
Group 2 participants will be villagers considered influential members of their community. In the first 2 months of the study, Group 2 participants will take part in four, 2-hour training sessions focusing on anti-stigma and anti-discrimination messages. Group 2 participants will also attend additional support meetings monthly, from Months 2 to 15. Group 2 participants will be evaluated before and after their training sessions to determine the improvements in knowledge and attitudes about HIV among group participants.
Group 3 participants will be randomly selected community members and will complete a cross-sectional survey at study entry and 6 and 12 months after Group 2's completion of training, to determine changing community attitudes about HIV as a result of Group 2's training. There will be no additional study visits or training for Group 3 participants.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | Participants will be HIV-infected villagers and will will take part in 2-hour skills training sessions every week from study entry to Week 8. Participants will bring a family member to each training session. After training, participants complete a post-training evaluation of the training sessions. Participants will also complete questionnaires at study entry and 6 and 12 months after completion of training. |
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| 2 | Experimental | Participants will be villagers considered influential members of their community. In the first 2 months of the study, Participants will take part in four 2-hour training sessions focusing on anti-stigma and anti-discrimination messages. Participants will also attend additional support meetings monthly, from Months 2 to 15. They will be evaluated before and after their training sessions to determine the improvements in knowledge and attitudes about HIV among group participants. |
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| 3 | Experimental | Participants will be randomly selected community members and will complete a cross-sectional survey at study entry and 6 and 12 months after Group 2's completion of training to determine changing community attitudes about HIV as a result of Group 2's training. There will be no additional study visits or training for Group 3 participants. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| HIV skills training program and questionnaire | Behavioral | Two-hour weekly skills training sessions followed by evaluation questionnaire |
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| Measure | Description | Time Frame |
|---|---|---|
| Medical Outcomes Study HIV Health Survey (MOS-HIV) score in-HIV infected participants | Throughout study |
| Measure | Description | Time Frame |
|---|---|---|
| Level of stigma among community members, as determined by HIV knowledge score and HIV attitudes and stigmatizing behaviors reported | Throughout study | |
| Emotional well-being of HIV-infected participants, as determined by perceived support scale and stigma scale scores |
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Inclusion Criteria for All Participants:
Inclusion Criteria for Group 1:
Inclusion Criteria for Group 2:
Inclusion Criteria for Group 3:
Exclusion Criteria for All Study Participants:
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| Name | Affiliation | Role |
|---|---|---|
| Zunyou Wu, MD, PhD | Centers for Disease Control and Prevention, China | Principal Investigator |
| Jie Xu, MD, MS | Centers for Disease Control and Prevention, China | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Chinese Center for Disease Control and Prevention | Beijing | 100050 | China |
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| Community-level stigma reduction program | Behavioral | Two-hour training sessions focusing on anti-stigma and anti-discrimination |
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| Cross-sectional survey | Behavioral | Survey evaluation of community attitudes towards HIV |
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| Throughout study |
| Self-efficacy score in HIV-infected participants | Throughout study |
| Knowledge of correct condom use score among HIV-infected participants | Throughout study |
| ID | Term |
|---|---|
| D015658 | HIV Infections |
| D012749 | Sexually Transmitted Diseases |
| ID | Term |
|---|---|
| D000086982 | Blood-Borne Infections |
| D003141 | Communicable Diseases |
| D007239 | Infections |
| D015229 | Sexually Transmitted Diseases, Viral |
| D016180 | Lentivirus Infections |
| D012192 | Retroviridae Infections |
| D012327 | RNA Virus Infections |
| D014777 | Virus Diseases |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
| D007153 | Immunologic Deficiency Syndromes |
| D007154 | Immune System Diseases |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| D011795 | Surveys and Questionnaires |
| D003430 | Cross-Sectional Studies |
| ID | Term |
|---|---|
| D003625 | Data Collection |
| D004812 | Epidemiologic Methods |
| D008919 | Investigative Techniques |
| D017531 | Health Care Evaluation Mechanisms |
| D011787 | Quality of Health Care |
| D017530 | Health Care Quality, Access, and Evaluation |
| D011634 | Public Health |
| D004778 | Environment and Public Health |
| D016021 | Epidemiologic Studies |
| D016020 | Epidemiologic Study Characteristics |
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