Improving Provider Counseling Interventions in HIV Practice
This trial is active, not recruiting.
|Treatment||stage based counseling|
|Sponsor||Johns Hopkins University|
|Collaborator||University of California, San Francisco|
|Start date||September 2003|
|End date||October 2007|
|Trial size||425 participants|
|Trial identifier||NCT00538993, H97HA01144|
Hypothesis: HIV clinicians trained to deliver brief counseling messages and receiving cues from a brief computer survey on risk behaviors of their patients can counsel have an impact on patient's risk behaviors.
|Intervention model||parallel assignment|
|Primary purpose||health services research|
Provider receives cue sheet to assist with counseling.
Provider does not receive cue sheet.
Disclosure of HIV status to sex partners; unprotected sexual encounters.
time frame: 12 months
Male or female participants at least 18 years old.
Inclusion Criteria: - HIV seropositive - English speaking Exclusion Criteria: - Cannot give informed consent
|Principal investigator||Emily Erbelding, M.D.|
|Description||This is a randomized controlled study. The purpose of this study is to assess the impact of the cue sheet as an aid to targeted provider behavioral counseling. All enrolled participants are HIV+ adults seen for regular medical care at a site affiliated with the Johns Hopkins AIDS Service. After consenting, participants will take an audio-assisted computer interviews to collect patient risk assessment data. For participants randomized to the intervention arm, the printed output on risk behaviors is then given to the provider along with cues for staged-based counseling for use during the same visit. Participants in the control arm take the same computerized risk assessment but there are no printed cue sheets. Risk behaviors of all participants are assessed at entry, at 6 months, and at 12 months. The main outcome measure is change in HIV transmission behaviors at 12 months for those in the intervention arm compared to the control arm.|
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