Optimizing the Floreciendo Sexual and Reproductive Health Workshop for Latina Teens and Fe
Floreciendo is a sexual and reproductive health workshop for Latina teens (ages 14-18 years) and their female caregivers (e.g., mothers, sisters, grandmothers). This study involves conducting a pilot optimization trial of Floreciendo using the multiphase optimization strategy (MOST) framework. The feasibility of using
| Condition(s) | Sexual Risk Behavior, Sexually Transmitted Infections, Unplanned Pregnancy |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | Floreciendo is a sexual and reproductive health workshop for Latina teens (ages 14-18 years) and their female caregivers (e.g., mothers, sisters, grandmothers). This study involves conducting a pilot optimization trial of Floreciendo using the multiphase optimization strategy (MOST) framework. The feasibility of using a 2 x 2 x 2 factorial trial design and the acceptability of the intervention components of Floreciendo will be examined. Effectiveness and implementation outcomes will be explored. This work will be conducted in partnership with community-based organizations in the Chicagoland area. |
| Who can participate | Inclusion criteria for teens: 1. Identify as Latina 2. Be 14-18 years old 3. Speak English and/or Spanish 4. Be available and have a female caregiver who is available for the workshop and research activities. 5. Be living with or in daily contact with the female caregiver. Inclusion criteria for female caregivers: 1. Be the mother or a female caregiver (e.g., aunt, sister, grandmother) of a Latina teen (aged 14-18 years old) 2. Be 19 years old or older 3. Speak English and/or Spanish 4. Be available and have a teen who is available for the workshop and research activities. 5. Be living with or in daily contact with the Latina teen. Latina teens and female caregivers must agree to participate as a dyad, and teens' refusal will supersede parental consent. Exclusion Criteria: Teens and caregi |
| Ages | 14 Years |
| Sex | All |
| Accepts healthy volunteers | Yes |
| Lead sponsor | University of Illinois at Chicago |
| Locations | Chicago, Illinois, United States; Chicago, Illinois, United States; Chicago, Illinois, United States; Cicero, Illinois, United States |
| Start date | 2024-03-09 |
| NCT ID | NCT06223165 |
| Official listing | https://clinicaltrials.gov/study/NCT06223165 |