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NCT Number: NCT07770438

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Dodoma, Dodoma, Tanzania

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About this study

Training for Health Professionals 2 Aim 3 is designed to evaluate the real-world effectiveness and feasibility of disseminating an Afrocentric sexual and reproductive health curriculum for health professional students in Tanzania. The study builds on prior Training for Health Professionals work, including a previous randomized controlled trial that showed improvements in sexual and reproductive health knowledge, attitudes, and clinical skills among health care students.

This Phase IV implementation study will be conducted at three institutions in Tanzania: the State University of Zanzibar, Kilimanjaro Christian University, and the University of Dodoma. The study will enroll medical, nursing, and midwifery students who are current pre-final year students at one of the participating institutions.

Participants will receive a four-day Afrocentric comprehensive sexual and reproductive health curriculum. The curriculum covers sexual health across the lifespan and male and female sexual dysfunctions on Day 1; key populations, including LGBT persons and sex workers, and sexual violence on Day 2; clinical skills training, ethics, and policy writing on Day 3; and community resources and cultural considerations on Day 4.

Participants will complete study surveys at baseline, immediately after the intervention, and at 3-month and 12-month follow-up. The surveys will assess sexual health knowledge, attitudes, and sexual history and counseling skills. Faculty involved in delivering the curriculum will also complete post-training evaluations assessing their knowledge, comfort, and skills in teaching the curriculum.

The study will evaluate whether participants increase and retain sexual health knowledge, attitudes, and skills after participating in the curriculum in a real-world educational setting. The study will also assess implementation fidelity and faculty training outcomes to inform future dissemination of the curriculum.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • 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

Exclusion criteria

  • 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
  • Prior exposure to the Training for Health Professionals curriculum or either of the previous pilots
  • Younger than 18 years of age
  • Non-English speaker
  • Unable to read
  • Employee of the researcher
  • Prisoner
  • Adult lacking capacity to consent or with diminished capacity to consent
  • Active member of the military or DoD personnel

Treatment and study plan

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.

Other names: Training for Health Professionals Curriculum

Primary outcomes

  1. Change in Sexual and Reproductive Health Knowledge

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

    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.

  2. Change in Sexual and Reproductive Health Attitudes

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

    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.

  3. Change in Sexual History Taking and Counseling Skills

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

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

B. R. Simon Rosser, PhD

CONTACT

[email protected]

612-624-0358

Koua A

CONTACT

[email protected]

612-626-3500

Sponsors and collaborators

Lead sponsor

University of Minnesota

Other

Collaborators

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

Registry information

Acronym: THP-2 Aim 3

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Aug 18, 2026
Registry last updated
Aug 18, 2026

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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