HIV and AIDS Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Women aged 18 years or older
- People who have a uterus
- People who do not have HIV (based on self-reporting)
- People who are not currently taking PrEP (a medication used to prevent HIV)
- People who are comfortable having conversations in English or Spanish
- People who are able to take part in the informed consent process (understanding and agreeing to the study details)
- Sexual and reproductive health clinicians who provide patient care at one of the participating clinic sites
- Clinic staff who work at one of the participating sites, whether or not their role involves direct patient contact
Who may not be able to join:
- People who are not able to become pregnant — for example, those who have had a hysterectomy (removal of the uterus) or tubal ligation (tubes tied)
- People who are hoping to become pregnant, as they would not qualify for the pregnancy prevention counselling part of the study
- People who already have a scheduled appointment with a member of the research team (this is to reduce the chance of study results being affected by prior contact)
- People who have already taken part in Aim 1 of this study are not eligible to also participate in Aim 2
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Jaimie P Meyer, MD, Yale Clinical and Community Research, Yale School of Medicine
Phone: 2034998075
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
PrEP initiation (prescribing); Feasibility of implementing the enhanced PrEP decision aid in SRH settings, according to the Proctor taxonomy; Acceptability of the enhanced PrEP decision aid within SRH settings, according to users (Proctor taxonomy); Penetration (reach) of the enhanced decision aid within SRH clinics (Proctor taxonomy); Penetration (reach) of the enhanced decision aid within SRH clinics (Proctor taxonomy); Penetration (reach) of the enhanced decision aid within SRH clinics (Proctor taxonomy); Adoption of the enhanced PrEP decision aid within SRH settings, according to users (Pr...
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.