FASTLANE II: Reducing Sex, Drug, and Mental Health Risk (NCT04109014) | Clinical Trial Compass
CompletedNot Applicable
FASTLANE II: Reducing Sex, Drug, and Mental Health Risk
United States20 participantsStarted 2021-05-03
Plain-language summary
The study uses a repeated measures, single group pretest-posttest design methodology to examine the feasibility, acceptability, and preliminary effectiveness of the FASTLANE II intervention aimed at decreasing risky sex behaviors among active methamphetamine using women. The study's methodology consists of two phases: 1) The feasibility and evaluation of recruitment capability and intervention effectiveness, and 2) qualitative acceptability interviews.
Who can participate
Age range
18 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Resident of San Antonio, Texas
* Female
* Mexican-American
* HIV-negative
* 18 years of age or older
* Self-identify as heterosexual
* Have had unprotected sex with at least one opposite sex partner during the previous 2 months
* Indicate that they have snorted or smoked methamphetamine at least once during the previous 2 months
Exclusion Criteria:
* Not a resident of San Antonio, Texas
* Male
* Not Mexican-American
* HIV-positive
* Younger than 18 years of age
* Do not self-identify as heterosexual
* Have not had unprotected sex with at least one opposite sex partner during the previous 2 months
* Indicate that they have not snorted or smoked methamphetamine at least once during the previous 2 months
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.