Skip to main content
OpenTrials
Not yet recruiting

NCT Number: NCT07781423

Nurse-Led PrEP Initiation Among Incarcerated Individuals

PrEP is a medication that can help prevent the spread of HIV, but many who might benefit from PrEP do not take it. Individuals experiencing incarceration are interested in starting PrEP while incarcerated, but there are challenges that make it difficult for them to start this medication when they return to the community. This study will test to see if a nurse-led, same-day PrEP start program can help individuals experiencing incarceration start and stay on PrEP. To do this, N = 90 PrEP-eligible patients during their incarceration will test the nurse-led program. Everyone will receive access to a nurse-led behavioral intervention during incarceration and information about PrEP services available in the community. Then, N = 60 participants will receive patient navigation support to help them link with PrEP care in the community and N = 30 participants will receive a list of community resources. Research interviews will be conducted with participants while they are incarcerated and 1, 3, and 6 months after they re-enter the community. Participants are offered compensation for each of the research interviews.

Not yet recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Currently incarcerated at the Rhode Island Department of Corrections
  • At least 18 years of age
  • Not currently pregnant
  • Eligible for PrEP
  • No PrEP use in the 90 days prior to incarceration
  • Interested in starting PrEP
  • Report any criminalized drug use or at least one heavy drinking day in the 90 days prior to incarceration
  • Likely to be incarcerated for more than a week but less than 6 months
  • Able to understand and speak English and provide written and verbal informed consent

Treatment and study plan

Nurse-led intervention

Behavioral

All participants will receive the nurse-led intervention. The study nurse will meet with participants twice during incarceration and deliver behavioral sessions focused on motivational interviewing and psychoeducation related to PrEP. The aim of these sessions is to enhance motivation to start PrEP following community re-entry. Anyone expressing interest in starting PrEP will be provided information about how to access PrEP care in the community with our study nurse and other community-based providers.

The study nurse will deliver same-day PrEP care services at a outpatient clinic. In this setting, the nurse will perform all of the necessary activities required to initiate a patient on same-day PrEP. These activities include, HIV testing and any other remaining recommended testing that was not performed while the participant was at RIDOC and placing an order for a PrEP prescription. All clinical activities will be supervised by a physician or a nurse-practitioner.

Patient Navigation Intervention

Behavioral

Participants randomly assigned to the experimental arm will receive a warm handoff from the study nurse to the patient navigator (PN), in which they will be introduced by the nurse to the PN prior to discharge. NAV participants will receive 6 monthly phone calls, or alternate means of contact (texts, emails, HIPAA compliant videoconferencing) if preferred by participant, from the PN and access to navigation services for 6 months. Navigation services include: assistance with health insurance issues, facilitating transfer of medical records, scheduling PrEP care appointments, and facilitating linkage to substance use treatment and mental health services as appropriate. In addition, the PN will remind participants of PrEP care appointments, arrange transportation to appointments as needed, and attend the first PrEP care appointment if desired by participant. The PN can also provide information regarding other community-based resources.

Standard-of-care (SoC)

Behavioral

SOC will consist of a brochure regarding how to receive PrEP care in the community after discharge from RIDOC, which SOC participants will receive from the study nurse prior to discharge.

Primary outcomes

  1. Linkage to Community-Based PrEP Care assessed with medical record review

    Time frame: 1, 3, & 6-Month Follow-ups

    Operationalized as receipt of prescription from a community-based provider within 6 months of release from incarceration. This will be verified through medical record review.

  2. Intervention Feasibility assessed with Exit Interviews

    Time frame: 6-Month Follow-up

    Participant eligibility rate, enrollment rate, rate of recruitment, and follow-up completion rate will serve as indices of intervention feasibility and will be compiled at the conclusion of the study. In exit interviews with NAV participants, feedback will be solicited regarding the feasibility of the intervention.

  3. Intervention Acceptability assessed with the Client Satisfaction Questionnaire-Revised

    Time frame: 6-Month Follow-up

    The 8-item Client Satisfaction Questionnaire-Revised will be administered to participants to assess intervention acceptability. Total scores range from 8 to 32, with higher scores representing greater intervention acceptability.

Secondary outcomes

  1. PrEP Care Retention

    Time frame: 3 & 6-Month Follow-up

    Retention in care is defined as attending a clinical appointment 3 months (+/- 1 month) after an initial PrEP care appointment. These data will be captured via medial record review.

  2. PrEP Adherence assessed with 3-item adherence measure

    Time frame: 1, 3, & 6-Month Follow-up

    PrEP adherence will be assessed via Wilson et al.'s 3-item adherence measure. This assessment is widely used and boasts favorable psychometric properties. Scores range from 0 to 30, with higher scores representing greater PrEP adherence.

Other outcomes

  1. Alcohol Use assessed with the Timeline Followback

    Time frame: Baseline, 1, 3, & 6-Month Follow-up

    The number of standard drinks consumed per day will be assessed with the Timeline Followback (TLFB) interview. The TLFB is a calendar-assisted structured interview which provides a way to cue memory and enhance recall. This data collection method has excellent reliability and validity.

  2. Drug Use assessed with the Timeline Followback

    Time frame: Baseline, 1, 3, & 6-Month Follow-up

    The class of drugs used each day will be assessed with the Timeline Followback (TLFB) interview. The TLFB is a calendar-assisted structured interview which provides a way to cue memory and enhance recall. This data collection method has excellent reliability and validity.

  3. HIV-Related Risk Behavior assessed with the HIV Risk Assessment Battery

    Time frame: Baseline, 1, 3, & 6-Month Follow-up

    The HIV Risk Assessment Battery (RAB) will be administered at each assessment period to capture participants' overall HIV acquisition risk. The RAB is a standardized measure with strong psychometric properties. Total scores range from 0 to 40, with higher scores representing greater HIV risk.

  4. Depressive Symptoms assessed with the Center for Epidemiologic Studies Depression Scale

    Time frame: Baseline, 1, 3, & 6-Month Follow-up

    The Center for Epidemiologic Studies Depression Scale (CES-D) will be used to assess depressive symptoms at baseline and follow-ups. This 20-item measure is widely used and has strong psychometric properties. Total scores range from 0 to 60, with higher scores representing greater depressive symptoms.

  5. Knowledge Regarding PrEP assessed with a PrEP Knowledge Questionnaire

    Time frame: Baseline, 1, 3, & 6-Month Follow-up

    PrEP knowledge will be assessed with a slightly-adapted 5-item measure that was developed to assess knowledge regarding PrEP. Scores range from 0 to 13, with higher scores representing greater PrEP knowledge.

  6. Attitudes and Beliefs Regarding PrEP Use assessed with PrEP Attitudes Survey

    Time frame: Baseline, 1, 3, & 6-Month Follow-up

    Attitudes and beliefs (norms, self-efficacy, and stigma) related to PrEP will be assessed with an adapted 9-item survey utilized in previous PrEP research. Scores range from 0 to 27, with higher scores representing greater stigmatizing attitudes related to PrEP.

  7. Treatment Received assessed with the Treatment Services Review

    Time frame: Baseline, 1, 3, & 6-Month Follow-up

    Receipt of case management, HIV/STI risk reduction counseling, mental health, substance use, and other treatment services will be assessed with the Treatment Services Review (TSR). This is a semi-structured method of assessing different types of treatment received. The number of times different types of treatment were utilized will be captured for each time period.

  8. Use of Medications assessed with semi-structured interview

    Time frame: Baseline, 1, 3, & 6-Month Follow-up

    Participants will be asked to provide information regarding their use of medications for medical, psychiatric, or substance use indications. The number of medications for each category (medical, psychiatric, and substance use indications) will be captured at each time point.

  9. Pregnancies assessed with semi-structured interview

    Time frame: Baseline, 1, 3, & 6-Month Follow-up

    Participants will also be asked about any pregnancies they have experienced.

  10. Reasons for PrEP Care Linkage/Non-Linkage assessed with qualitative exit interview

    Time frame: 6-Month Follow-up

    Brief qualitative exit interviews will be conducted with NAV participants (n = 60). These participants will be asked to reflect on factors that impacted their use or non-use of PrEP while incarcerated and after release and about other HIV risk reduction strategies used. Participants who linked with a community-based PrEP care provider will be asked about the decision process for their PrEP formulation choice (daily oral vs. long acting). Lastly, we will ask about perceived utility of the nurse-led and NAV intervention components and suggested changes.

  11. Mistrust of Medial Organizations assessed with the Medical Mistrust Index

    Time frame: Baseline, 1, 3, & 6-Month Follow-up

    Mistrust of medical organizations will be assessed with the Medical Mistrust Index (MMI) The MMI is well suited for assessing medical mistrust of organizations and has been validated among various racial and ethnic groups. Scores range from 7 to 28, with higher scores representing greater mistrust of medical organizations.

  12. Mistrust of Medical Personnel assessed with the Group Based Medical Mistrust Scale

    Time frame: Baseline, 1, 3, & 6-Month Follow-up

    Mistrust of medical personnel will be assessed with the Group Based Medical Mistrust Scale (GBMMS). The GBMMS boasts strong psychometric properties and has been validated in various racial and ethnic groups. Scores range from 12 to 60, with higher scores representing greater mistrust of medical personnel.

Study contacts

Contact information is provided by the study sponsor or research team.

Evan Ames

CONTACT

[email protected]

401-444-2474

Susan Ramsey, PhD

CONTACT

[email protected]

401-444-7831

Sponsors and collaborators

Lead sponsor

Rhode Island Hospital

Other

Registry information

Official study title

Nurse-Led Rapid Initiation of HIV Pre-Exposure Prophylaxis Care Among Incarcerated Individuals With Continuation of Care Services Post-Incarceration

Acronym: SWIFT

Important dates

Study start
2026
Primary completion
2027
Study completion
2028
First posted
Aug 24, 2026
Registry last updated
Aug 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.