Skip to content

Ending Sexual Harassment - Teaching Of Principal Investigators

Ending Sexual Harassment - Teaching Of Principal Investigators

Status
Enrolling by invitation
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06171633
Acronym
E-STOP
Enrollment
2160
Registered
2023-12-14
Start date
2024-03-06
Completion date
2027-06-30
Last updated
2025-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sexual Harassment

Keywords

Sexual Harassment Prevention, Educational Online Training, Video Game Elements, Upstanding

Brief summary

The study targets three aims: Aim 1: focuses on PIs' and mentors' confidence in their ability to intervene on sexual harassment and their attitudes, perceptions, and knowledge (APK) about sexual harassment, civility, microaggressions, and unconscious bias. Aim 2: focuses on trainees' experiences of sexual harassment and microaggressions and civility, sense of belonging, well-being, productivity, and persistence in a research career. Aim 3: focuses on the culture and climate of the research learning environment.

Detailed description

Participants (PIs, mentors, and trainees), starting in year one, will be asked to complete a baseline survey (using the secure survey software Qualtrics) regardless of condition assignment. Then, for several months, PIs, mentors, and mentees will receive virtual educational materials (presented using a Learning Management System) appropriate to the condition to which their program has been randomized. The initial post-survey for PIs and mentors will be shortly after the final module to evaluate short-term outcomes, encompassing attitudes, perceptions, and knowledge. Subsequently, the second post-survey will be administered one year later. Trainees will participate in three post-surveys: one immediately after, another one year later, and a final one two years later.

Interventions

BEHAVIORALE-STOP online educational program (treatment condition)

Participants access online video modules through an online learning platform. Program includes modules on civility and upstander interventions and education about sexual harassment, microaggressions, and implicit bias.

BEHAVIORALE-STOP online educational program (control condition)

Participants access online video modules through an online learning platform. Program includes authorship ethics only.

Sponsors

National Institute of General Medical Sciences (NIGMS)
CollaboratorNIH
Stanford University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* PIs, Mentors and Trainees of T-32 Programs

Exclusion criteria

* People who are not PIs, Mentors and Trainees of T-32 Programs

Design outcomes

Primary

MeasureTime frameDescription
Confidence to Intervene on Sexual Harassment Scale ScoreSurvey at baseline, immediately post-intervention (9 months after baseline), and 1 year after the completion of the 9-month interventionParticipants are asked to rate: How confident are you in your ability to intervene when you hear about or witness sexual harassment? Score range: 1 (not at all confident) to 5 (extremely confident).

Secondary

MeasureTime frameDescription
Persistence in research careersbaseline, immediately post-intervention (9 months after baseline), and 1 year after completion of the 9-month intervention.Participants are asked to rate: How extensively do you expect to be involved in research during your medical career? Score range 1 (not involved) to 5 (exclusively)
Experiences of sexual harassment as measured by the short Sexual Experiences Questionnaire (SEQ-DoDs)baseline, immediately post-intervention (9 months after baseline), and 1 year after completion of the 9-month intervention.The SEQ consists of 4 domains: gender harassment--sexist hostility (4 questions); gender harassment--sexual hostility (4 questions); unwanted sexual attention (4 questions); and sexual coercion (4 questions); the score for each question ranges from 1 (never) to 5 (many times); scores for questions within each domain are summed and divided by the number of questions, resulting in an average score range from 1 (never) to 5 (many times) for each domain.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026