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Evaluating the Effects of Reproductive Health Training on Provider Behavior (THP-2)

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Active, not recruiting

Conditions

Training
Health Knowledge, Attitudes, Practice

Treatments

Behavioral: Comprehensive sexual health curriculum

Study type

Interventional

Funder types

Other

Identifiers

NCT06428058
R01HD092655 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The goal of this randomized, controlled, single blinded trial is to evaluate the medium to long-term effects of an Afrocentric sexual health curriculum on health professional students' knowledge, attitudes, and clinical skills in providing sexual health in Tanzania.

Full description

All enrollees will be health students at MUHAS recruited through announcements in class, flyers on student noticeboards, and email. Students who are interested in learning more about the study can do so by asking questions of the recruiting faculty member, by going to, telephoning, or emailing the study office (at MUHAS). Students can also visit the study website. In addition, all students who contact the office will be given a copy of a flyer advertising the study and a copy of the consent documents to preview prior to participation. Students contacting the office by email will be sent electronic versions of the same documents.

Participants in Aim 1 are informed to schedule an appointment (in the month prior to the seminar) to complete a pre-evaluation. At the study site, participants complete pen and paper surveys, and are videotaped interviewing two standardized patients. Next, participants are randomized to either the intervention or waitlist control condition. Participants in the intervention will attend the 4-day sexual health seminar and complete a short post-test. In addition, at 6- and 12-month follow-up after the pre-test, participants in both arms complete surveys and two videotaped interviews (at each follow-up) and a final survey at 24-month follow-up. At the end of the study, participants assigned to the control condition can attend the seminar.

Enrollment

310 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • A health student studying at MUHAS and verified by being registered as a pre-final year midwifery, nursing or medical student (or its equivalent).
  • "Pre-final" year is defined as a student who is just about to enter year 3 of nursing, or year 4 of midwifery or medicine.
  • Living or studying in Tanzania
  • Experienced, operationalized as having worked at least 100 hours as a health worker in a clinic, hospital or community setting so students can discuss what happens in the clinical setting
  • Able to speak English and Kiswahili.

Exclusion criteria

  • Students who will not be able to attend all days of the seminar at their health institution or be on their campus for the follow-up.
  • Students who express any reservations about attending (e.g., due to religious objections)
  • Students who express a fear of violence due to attending (e.g., from a spouse or relative).
  • Students who attended the sexual health seminar (e.g., during THP-1 or at another site). This is to prevent a student participating more than once.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

310 participants in 2 patient groups

Comprehensive Sexual Health Curriculum
Experimental group
Description:
Participants received a four-day comprehensive sexual health curriculum tailored for Africa.
Treatment:
Behavioral: Comprehensive sexual health curriculum
Waitlist Control
No Intervention group
Description:
Participants in this arm completed a follow-up survey and scheduled to receive the intervention after the end of the trial.

Trial contacts and locations

1

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Central trial contact

B.R. Simon Rosser, PhD; Michael Ross, PhD

Data sourced from clinicaltrials.gov

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