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Clinical Trials/NCT04320186
NCT04320186
Completed
N/A

Community Influences Transitions in Youth Health II - Center for the Study of Community Health

University of Alabama at Birmingham1 site in 1 country334 target enrollmentApril 3, 2015

Overview

Phase
N/A
Intervention
Not specified
Conditions
Sexually Transmitted Diseases
Sponsor
University of Alabama at Birmingham
Enrollment
334
Locations
1
Primary Endpoint
Perceived HIV-related Stigma
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The purpose of this protocol is to develop and evaluate an HIV prevention Entertainment Education (EE) intervention aimed at reaching underserved, at-risk African Americans, aged 18-25 years, living in disadvantaged urban neighborhoods in the Birmingham area.

Detailed Description

The goal of this 5 year project is to promote HIV testing and improve HIV-related risk behaviors (e.g. condom use, substance use before sex, regular Sexually Transmitted Infection (STI) testing) via population-sensitive and population-specific HIV prevention videos that are appealing, evidence-based, scalable, and sustainable to the target population. Formative research was conducted in Phase I (Year 1-2), to pre-test the questionnaire and gather in-depth data (via focus groups, intercept interviews, and individual structured interviews) to inform intervention development. Phase 2 of the project involved developing, delivering, and subsequently evaluating the efficacy of peer-driven EE HIV prevention messaging to broader social networks via a social media platform, with the platform contingent on formative data. An HIV education video series, "The Beat HIVe", was produced and served as intervention materials for the quasi-experimental research project. Respondent Driven Sampling (RDS) was used to access and use the social networks of high-risk youths as channel and agents for change. RDS is a recent innovative adaptation of chain-referral network sampling that provides peer-driven access to hard-to-reach subpopulations while reducing sampling biases associated with conventional snowball sampling.

Registry
clinicaltrials.gov
Start Date
April 3, 2015
End Date
December 31, 2020
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Susan Davies

Professor

University of Alabama at Birmingham

Eligibility Criteria

Inclusion Criteria

  • African American young adults Aged 18-25 Living in the Birmingham USA Competent to give informed consent

Exclusion Criteria

  • Obvious psychosis, dementia, inability to hear. Plan to move within the next 6 months

Outcomes

Primary Outcomes

Perceived HIV-related Stigma

Time Frame: 6 months

The scores are scaled in the positive direction implying that the higher the score, the higher the level of stigma. The possible overall stigma score ranges from 40 to 160, low-level stigma is between 25th percentile and 50th percentile (40-80), middle-level stigma is between 50th percentile and 75th percentile (81-120), while high-level stigma is for values greater than 75th percentile (121-160).

Condom Use Self-Efficacy Scale

Time Frame: 3 months

This is a 28 item self-report questionnaire which elicits responses using a five-point Likert scale format, ranging from 'strongly disagree' to 'strongly agree'. Each of the responses is scored as follows: 'strongly disagree' = 0, 'disagree' = 1, 'undecided' = 2, 'agree' = 3 and 'strongly agree' = 4. After reversing for negatively worded items, scores are summed. The possible range of scores is 0-112, with higher scores indicating greater condom use self-efficacy.

HIV Knowledge Questionnaire-18

Time Frame: 6 months

This scale assess an individual level of HIV-related knowledge. For each of the 18 true/false, HIV- related questions, a score of 1 was assigned to each 'correct' answer. Assessments were based on the analysis of the summation of these scores, which had a possible range of 0 to 18, whereby higher scores indicated greater knowledge of HIV.

Secondary Outcomes

  • HIV Testing Questionnaire(6 months)
  • Timeline Followback(6 months)

Study Sites (1)

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