NCT07218848
ProSalud in Latinos Living in Rural/Agricultural Communities Within Moffitt's Catchment Area
Active, Not Recruiting
NAAges 18+InterventionalPreventionH. Lee Moffitt Cancer Center and Research InstituteInvestigator-initiated
~52 participants
Updated 2026-05-22 on ClinicalTrials.gov
What's tested:Aim 1 WorkshopsAim 2 Focus Groups
At a glance
Recruiting sites
0 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Acceptability
Measured over 1 year
+2 more outcomes measured
Conditions
Where it's being run
2 sites across 1 statesFlorida2
Study leadership
- Peter Kanetsky, MPH, PhD · PRINCIPAL_INVESTIGATOR · Moffitt Cancer Center
- Marilyn Stern, PhD · PRINCIPAL_INVESTIGATOR · University of South Florida
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Eligibility criteria
Inclusion
We will include adults of any age and sex who are parents of a 6- to 12-year-old child. Parents must speak Spanish and be able to read and write at the 4th-grade level. Parents who speak English in addition to Spanish can also take part in the study, always considering that the workshop will be conducted in Spanish.
Individuals who are wards of the state will be excluded from participation in this study.
If a participant chooses not to take part at any point, they may do so without any consequences or loss of services provided through RCMA. This ensures that their rights are protected, and their decision will not affect their access to any services or support.
We may, by chance, include students and employees. However, we do not plan on collecting information that would indicate any of these statuses. No wards will be included in the study. Wards will not be included as research participants. Because recruitment will happen through RCMA, we anticipate most participants to be socially and/or economically disadvantaged. Participation in this study is entirely voluntary.
What this trial measures
- Acceptability1 year
Acceptability will be confirmed if ≥80% of enrolled participants indicate an intention to implement behavioral recommendations.
- Demand feasibility and adherence1 year
The study will be considered feasible if ≥75% of eligible parents approached to participate in the study agree to enroll.
- Implementation feasibility1 year
Implementation feasibility will be established if 100% of data collection is completed in the 1-year timeframe.