- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT00183638
A Tailored Interactive Website for Promoting Condom Use Among Young Adults (Youthnet)
Randomized Controlled Trial to Establish Efficacy of a Website to Promote Condom Use for Adults Aged 18-25
연구 개요
상태
상세 설명
Adolescents and young adults are at the greatest risk for acquiring a sexually transmitted disease (STD). Approximately 3 million people between the ages of 18 and 24 become infected with an STD each year. Education about the risks and consequences of unprotected sex is a powerful tool that can be used to prevent or reduce the risk of infection. The program in this study will deliver messages to educate participants about condom use and the risk of STD infection. The study will evaluate the effectiveness of a tailored interactive online risk reduction program versus a standard online risk reduction program in reducing the risk of STD infection in young adults.
Participants in this open-label study will be recruited from one of two clinics in the Denver, Colorado area: Denver Metropolitan Health Clinic or Planned Parenthood of the Rocky Mountains. Participants will be randomly assigned to receive internet-based messages from either the Youthnet program or the control program while filling out a risk assessment survey. Participants in the Youthnet program will be asked their gender and ethnicity so they may be assigned to a role model of the same gender and ethnicity via a computer program. This role model will appear online 5 times during the survey to deliver interactive messages that will be tailored to HIV/STD risk reduction and will specifically address attitudes about condom usage. The control program will deliver 5 general, non-tailored messages containing information on reproductive health not specific to condoms or STDs. Participants will be assessed at baseline and a follow-up session 3 months after enrollment. Frequency of condom use and attitudes toward condom use will be assessed using behavioral scales.
연구 유형
등록 (실제)
단계
- 2 단계
연락처 및 위치
연구 장소
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Colorado
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Aurora, Colorado, 미국, 80045-0508
- University of Colorado Health Sciences Center
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Client of Denver Metropolitan Health Clinic or Planned Parenthood
- English-speaking
- Access to a computer and an existing e-mail account
- Will be in Denver for at least 4 months
Exclusion Criteria:
- Not a resident of the Denver metropolitan area
- No existing e-mail address
- No access to a computer
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 방지
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: 1
Participants will receive Internet-based tailored prevention messages
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Participants will receive five 30-second flash clips promoting condom norms, positive attitudes, self-efficacy, and risk awareness.
Participants in the Youthnet program will be asked their gender and ethnicity so they may be assigned to a role model of the same gender and ethnicity via a computer program.
This role model will appear online 5 times during the survey to deliver interactive messages that will be tailored to HIV/STD risk reduction and will specifically address attitudes about condom usage.
다른 이름들:
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활성 비교기: 2
Participants will receive non-tailored messages containing information on reproductive health
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The control program will deliver five general, non-tailored messages containing information on reproductive health not specific to condoms or STDs.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
|
Condom use with non main partners
기간: Measured at Month 3
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Measured at Month 3
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2차 결과 측정
결과 측정 |
기간 |
|---|---|
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Self-efficacy for condom use and condom negotiation
기간: Measured at Month 3
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Measured at Month 3
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Attitudes and norms towards condom use
기간: Measured at Month 3
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Measured at Month 3
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공동 작업자 및 조사자
수사관
- 수석 연구원: Sheana S. Bull, PhD, University of Colorado, Denver
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .