Evaluating the Effects of Reproductive Health Training on Provider Behavior - Aim 3

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Minnesota

About this trial

This study will evaluate the real-world effectiveness of a four-day Afrocentric sexual and reproductive health curriculum for health professional students in Tanzania.

Medical, nursing, and midwifery students from the State University of Zanzibar, Kilimanjaro Christian University, and the University of Dodoma will receive the curriculum. The curriculum covers sexual health across the lifespan, sexual dysfunctions, key populations, sexual violence, clinical skills training, ethics, policy writing, community resources, and cultural considerations.

Student outcomes will be assessed using surveys at baseline, immediately after the curriculum, and at 3-month and 12-month follow-up to examine changes in sexual health knowledge, attitudes, and sexual history and counseling skills.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Current pre-final year student at the State University of Zanzibar, Kilimanjaro Christian University, or the University of Dodoma in midwifery, nursing, or medicine

Able to attend the full 4-day training

Fluent in English and Kiswahili

Willing to volunteer to complete all evaluation procedures

Disqualifiers

Unable to attend all days of the seminar at SUZA, KCMC, or UDOM

Unable to be on the SUZA, KCMC, or UDOM campus for the follow-up dates

Expresses reservations about attending, including religious objections

Expresses fear of violence due to attending, including fear from a spouse or relative

Trial design

Design model

Single group

Treatments tested in this trial

  • Afrocentric Sexual and Reproductive Health Curriculum

    Behavioral

    The intervention is a four-day Afrocentric comprehensive sexual and reproductive health curriculum. It covers sexual health across the lifespan, male and female sexual dysfunctions, key populations including LGBT persons and sex workers, sexual violence, clinical skills training, ethics, policy writing, community resources, and cultural considerations.

Treatment groups

650 Participants
are divided into 1 treatment group
Group A: Afrocentric Sexual and Reproductive Health CurriculumExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in Sexual and Reproductive Health Knowledge

Change in sexual and reproductive health knowledge will be assessed using participant survey responses collected before the curriculum, immediately after the curriculum, and at 3-month and 12-month follow-up.

Time frame
Baseline, immediately post-intervention, 3 months, and 12 months
2

Change in Sexual and Reproductive Health Attitudes

Change in attitudes related to sexual and reproductive health care will be assessed using participant survey responses collected before the curriculum, immediately after the curriculum, and at 3-month and 12-month follow-up.

Time frame
Baseline, immediately post-intervention, 3 months, and 12 months
3

Change in Sexual History Taking and Counseling Skills

Change in sexual history taking and counseling skills will be assessed using participant survey responses collected before the curriculum, immediately after the curriculum, and at 3-month and 12-month follow-up.

Time frame
Baseline, immediately post-intervention, 3 months, and 12 months

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Minnesota

Lead sponsor

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborator