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Ending Sexual Harassment - Teaching Of Principal Investigators (E-STOP)

Stanford University logo

Stanford University

Status

Invitation-only

Conditions

Sexual Harassment

Treatments

Behavioral: E-STOP online educational program (control condition)
Behavioral: E-STOP online educational program (treatment condition)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06171633
66842
1R01GM147063 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full 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.

Enrollment

2,160 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • PIs, Mentors and Trainees of T-32 Programs

Exclusion criteria

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

2,160 participants in 4 patient groups

Intervention Group / year 1
Experimental group
Description:
Beginning in year 1, participants access online video modules through an online learning platform for up to 9 months.
Treatment:
Behavioral: E-STOP online educational program (treatment condition)
Control Condition Group / year 1
Experimental group
Description:
Beginning in year 1, participants access online video modules through an online learning platform for up to 9 months.
Treatment:
Behavioral: E-STOP online educational program (control condition)
Intervention Group / year 2
Experimental group
Description:
Beginning in year 2, participants access online video modules through an online learning platform for up to 9 months.
Treatment:
Behavioral: E-STOP online educational program (treatment condition)
Control Condition Group / year 2
Experimental group
Description:
Beginning in year 2, participants access online video modules through an online learning platform for up to 9 months.
Treatment:
Behavioral: E-STOP online educational program (control condition)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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