- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05048290
Communication Skills to Build a Diverse Biomedical Workforce
Building a Diverse Biomedical Workforce Through Communication Across Difference
Study Overview
Status
Conditions
Detailed Description
PRIMARY OBJECTIVES:
I. Determine communication across difference (CAD) workshop effects over time using experimental and control dyads of summer students and their matched junior mentors.
Ia. Develop and deliver CAD skills workshops to dyads of students and junior mentors.
Ib. Test CAD workshop effects for individual participants with pre-, post-, and follow-up surveys of model variables over the course of the intervention.
II. Identify causal relationships of the social-influence variables with experimental and control groups of dyads over the 9-month course of the intervention.
IIa. Assess the psychological processes and causal relationships for students linking CAD to career intentions.
IIb. Assess the psychological processes and causal relationships for junior mentors linking CAD to career intentions and intentions to mentor diverse students in the future.
IIc. Assess the paired interaction effects between dyad members using pre-, post-, and follow-up model variables over the course of the intervention.
III. Assess long-term outcomes of the intervention and predictive utility of the student and mentor models by measuring changes in Hallmarks of Success: distal career persistence and network growth for students and junior mentors, as well as junior mentors' engagement in mentoring of diverse students.
OUTLINE: Dyads of summer students and their matched junior mentors are assigned to 1 of 2 groups.
GROUP I (EXPERIMENTAL): Participants complete 2 communication workshops about conversational skills and development of a video about the summer student's research experience over 3 hours each during the second week of the summer research experience and 2-3 weeks before the conclusion of summer experience. Participants also complete surveys over 15 minutes each about their communication, their engagement with research, mentoring experience, and current career intentions, before participating in the workshop, after the second workshop and at 6 months after the conclusion of the summer experience.
GROUP II (CONTROL): Participants complete 2 generic communication workshops about networking and presentation skills over 3 hours each during the second week of the summer experience and 2-3 weeks before the conclusion of summer experience. Participants also complete surveys over 15 minutes each about their communication, their engagement with research, mentoring experience, and current career intentions, before participating in the workshop, after the second workshop and at 6 months after the conclusion of the summer experience.
Study Type
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Texas
-
Houston, Texas, United States, 77030
- Recruiting
- M D Anderson Cancer Center
-
Contact:
- Carrie Cameron
- Phone Number: 713-794-1476
- Email: ccameron@mdanderson.org
-
Principal Investigator:
- Carrie Cameron
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- FOR SUMMER STUDENTS: Currently an undergraduate, medical student, or early Master's or Doctor of Philosophy (PhD) level student who is participating in a structured summer research program and receiving daily research supervision from a junior mentor (defined as a Master's or PhD level graduate student, a postdoctoral fellow, or an instructor) within a faculty member's research team
- FOR JUNIOR MENTORS: Currently a Master's or PhD student; postdoctoral trainee; or instructor working within a faculty member's research team and supervising a summer research student
Exclusion Criteria:
- FOR SUMMER STUDENTS: High school students
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group I (communication workshops, video, surveys)
Participants complete 2 communication workshops about conversational skills and development of a video about the summer student's research experience over 3 hours each during the second week of the summer research experience and 2-3 weeks before the conclusion of summer experience.
Participants also complete surveys over 15 minutes each about their communication, their engagement with research, mentoring experience, and current career intentions, before participating in the workshop, after the second workshop and at 6 months after the conclusion of the summer experience.
|
Complete surveys
Participate in communication workshops
Participate in generic communication skills workshops
Develop a video
Other Names:
|
|
Active Comparator: Group II (generic communication workshops, surveys)
Participants complete 2 generic communication workshops about networking and presentation skills over 3 hours each during the second week of the summer experience and 2-3 weeks before the conclusion of summer experience.
Participants also complete surveys over 15 minutes each about their communication, their engagement with research, mentoring experience, and current career intentions, before participating in the workshop, after the second workshop and at 6 months after the conclusion of the summer experience.
|
Complete surveys
Participate in communication workshops
Participate in generic communication skills workshops
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Degree completion rates
Time Frame: Through study completion, an average of 1 year
|
Will be assessed in both summer students and junior mentors.
|
Through study completion, an average of 1 year
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Carrie Cameron, M.D. Anderson Cancer Center
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2019-1010 (Other Identifier: M D Anderson Cancer Center)
- NCI-2020-04436 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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