52 Participants Needed

Virtual Promotoras Program for Sexual Health

Age: < 65
Sex: Female
Trial Phase: Academic
Sponsor: University of Alabama, Tuscaloosa
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

Trial Summary

What is the purpose of this trial?

Young Latina women face significant barriers to sexual health and healthcare access, particularly in emerging Latino states like Alabama. The goals of the proposed study are to develop and examine the feasibility of an innovative, scalable mHealth, "safe space" intervention for Young Latina Women (YLW) in Alabama (AL) and to stimulate the conduct of behavioral research at the University of Alabama. This work is consistent with the National Institute of Nursing Research's goals of "Enhancing wellness by understanding the physical, behavioral, cultural and environmental influences on health status and developing culturally tailored interventions to prevent illness and promote health" and "Using innovative technologies to develop novel interventions that deliver personalized care and real-time health information to patients, families and healthcare providers".

Eligibility Criteria

This trial is for young Latina women aged 16-21 in Alabama who identify as Latina, haven't had a preventive or sexual healthcare visit in the last 18 months, and have lived in Alabama for at least 5 years.

Timeline

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Intervention Development

Development and feasibility testing of the mHealth VIP Program, including educational modules and virtual promotoras guidance

3 months

Follow-up

Participants are monitored for sexual health and healthcare access empowerment using the Sexual and Reproductive Empowerment Scale

4 weeks

Treatment Details

Interventions

  • Virtual Promotoras Program
Trial Overview The study is testing an mHealth 'safe space' intervention called the Virtual Promotoras Program. It aims to improve sexual health among these women by providing personalized care and real-time health information.
Participant Groups
1Treatment groups
Experimental Treatment
Group I: Single Arm: Virtual Promotoras InterventionExperimental Treatment1 Intervention
Single-arm study. Pre and post intervention. Observational. Behavioral

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Alabama, Tuscaloosa

Lead Sponsor

Trials
49
Recruited
17,900+
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