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Completed

NCT Number: NCT02405481

SEPA III: The Effectiveness Trial

The study evaluates the effectiveness of SEPA (Salud, Educacion, Prevencion y Autocuidado; Health, Education, Prevention and Self-Care) to increase HIV prevention behaviors and to reduce the incidence of STIs for Hispanic women when delivered in a real-world setting by community agency personnel. The study recruits Hispanic women between the ages of 18 and 50 who are sexually active and are randomized to either SEPA or a Wait-List Control condition.

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Key information

Conditions

Age range

18 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Miami

Miami, Florida, 33136, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Hispanic Women,
  • 18 to 50 years old,
  • Sexually active in the past three months

Exclusion criteria

  • Non-Hispanic,
  • younger than 18,
  • older than 50,
  • not sexually active

Treatment and study plan

SEPA III

Behavioral

Primary outcomes

  1. Condom Use

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

University of Miami

Other

Registry information

Acronym: SEPA III

Important dates

Study start
2013
Primary completion
2016
Study completion
2016
First posted
Apr 1, 2015
Registry last updated
May 22, 2018

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.

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