National Research Mentoring Network Studies, Phase II: Multi-Study Common Measures Data, United States, 2019-2024 (ICPSR 39676)
Version Date: Mar 10, 2026 View help for published
Principal Investigator(s): View help for Principal Investigator(s)
Christine Pfund, University of Wisconsin-Madison
https://doi.org/10.3886/ICPSR39676.v1
Version V1
Alternate Title View help for Alternate Title
Summary View help for Summary
The National Research Mentoring Network (NRMN), an initiative within the National Institutes of Health's Diversity Program Consortium (DPC), was established to support the career development of individuals from diverse backgrounds in biomedical research, with a focus on mentorship and professional development. In its first phase (2014-2019), the NRMN built a network of mentors and mentees from a variety of disciplines, from over 10,000 individuals and over 7,000 mentors and mentees engaged in research mentorship training or grantsmanship coaching. Phase II (launched in 2019) built on this foundation by investigating longer-term outcomes and identifying mentorship strategies, particularly for diverse populations. This phase reimagined the NRMN as a consortium consisting of one coordination center (the NRMN Coordination Center (CC)), a resource center (the NRMN Resource Center) and 10 independent research studies that focused on mentorship, career development, and professional networking. These studies shared a common goal of exploring how specific mentorship practices influence career outcomes for diverse groups in biomedical research.
The multi-study common measures dataset of NRMN contains data collected using common measures across 10 independent research studies conducted under NRMN Phase II (2019-2024), part of the National Institutes of Health (NIH) Diversity Program Consortium (DPC). Each study implemented mentorship and career development interventions targeting individuals from diverse backgrounds in biomedical research. While study designs and populations varied, all agreed to collect a shared data using a set of community-defined common measures. The common measures dataset was compiled using codebooks and documentation provided by study teams. Where full survey instruments were unavailable, variables were mapped from available materials and cross-checked for consistency. This dataset supports research on mentorship, professional development, and career outcomes in biomedical research.
Citation View help for Citation
Export Citation:
Funding View help for Funding
Subject Terms View help for Subject Terms
Geographic Coverage View help for Geographic Coverage
Smallest Geographic Unit View help for Smallest Geographic Unit
College institution
Distributor(s) View help for Distributor(s)
Time Period(s) View help for Time Period(s)
Date of Collection View help for Date of Collection
Data Collection Notes View help for Data Collection Notes
- Additional Information: For additional information on the National Research Mentoring Network Studies, Phase II: Multi-Study Common Measures Data study, please visit the National Research Mentoring Network Studies website.
Study Purpose View help for Study Purpose
The purpose of the study is to explore how specific mentorship practices influence career outcomes for diverse groups in biomedical research.
Study Design View help for Study Design
Each of the 10 National Research Mentoring Network (NRMN) Phase II research studies consisted of a set of research aims, intervention models, recruitment strategies, and data collection designs. All studies led interventions for multiple groups of participants, with more than half of the studies leading interventions for ten or more separate cohorts. Most interventions were conducted virtually between October 2020 and June 2024. Recruitment strategies varied across studies, with some employing site-specific recruitment to target participants from particular institutions and others using national recruitment strategies to reach participants from a wide range of geographic regions and institutions. At least one study utilized both site-specific and national recruitment strategies. Study participants ranged from undergraduate students to faculty from hundreds of universities and institutions across all US regions, including public and private universities, minority-serving institutions, and research institutions. The data collection design for each study varied; however, all studies administered baseline surveys (pre-intervention) and post-surveys (post-intervention). The majority of studies also employed longitudinal study designs, with survey timepoints ranging from 3 months post-intervention to 48 months post-intervention. Survey measures were determined by each study, although all studies agreed to use a set of community-agreed-upon common measures.
To support systematic and consistent tracking of research activities across the 10 NRMN studies, tracking spreadsheets were created for each study. These spreadsheets were used to collect detailed information on various aspects of the research, including project design, recruitment strategies, participant enrollment, intervention timelines, survey design, survey administration, and the usage of common measures. Both the Mentoring Network Coordination Center (NRMN CC) and designated members from each study's research team had access to the tracking spreadsheets, enabling collaboration, sharing of updates, and confirmation of the accuracy of the recorded information. The NRMN CC managed an Institutional Review Board (IRB) protocol at the University of Wisconsin-Madison to securely transfer data from the participating research studies. Research teams were instructed to upload common measure survey data periodically into a secure folder in University of Wisconsin-Madison Box, a cloud storage platform. The first set of common measures data was received in March 2021, with final data requests sent to the researchers in April 2024, two months before the official end of the 5 year grant period. Data that could not be transferred by the requested deadline from studies were excluded. Upon receipt, the data files were reviewed by NRMN CC researchers for consistency and quality. Any data that did not correspond to the agreed upon common measures were excluded from the dataset. Once verified, the common measures data from all participating studies were compiled into a unified dataset and was structured to ensure compatibility across studies.
Sample View help for Sample
The data collection contains 12,655 survey responses from the 10 research teams with 5,620 unique respondents.
Time Method View help for Time Method
Universe View help for Universe
Mentors and Mentees in the Biomedical Research Field in the United States.
Unit(s) of Observation View help for Unit(s) of Observation
Data Type(s) View help for Data Type(s)
HideOriginal Release Date View help for Original Release Date
2026-03-10
Version History View help for Version History
2026-03-10 ICPSR data undergo a confidentiality review and are altered when necessary to limit the risk of disclosure. ICPSR also routinely creates ready-to-go data files along with setups in the major statistical software formats as well as standard codebooks to accompany the data. In addition to these procedures, ICPSR performed the following processing steps for this data collection:
- Performed consistency checks.
Notes
These data are freely available to data users at ICPSR member institutions. The curation and dissemination of this study are provided by the institutional members of ICPSR. How do I access ICPSR data if I am not at a member institution?