- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06113926
Racial Discrimination, Pain, and the Buffering Influences of Acknowledgment
October 27, 2023 updated by: Katarina AuBuchon, George Washington University
Black young adults (aged 18-30; N = 92) were racially included (i.e., received the ball an equal number of times) or excluded (i.e., received the ball only once) by other White players in a ball-tossing computer game called Cyberball; White experimenters acknowledged the exclusion for half of the excluded participants.
Participants completed a cold-pressor task twice to measure pain sensitivity (threshold, tolerance, and unpleasantness): immediately prior, and after the Cyberball (and acknowledgment) manipulation.
Participants also completed a post-manipulation survey examining the psychological effects of racial exclusion and acknowledgment (i.e., psychological needs satisfaction, negative affect, control).
Study Overview
Study Type
Interventional
Enrollment (Actual)
92
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
District of Columbia
-
Washington, District of Columbia, United States, 20052
- The George Washington University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Participants identify as Black/African American
- Age 18-30
Exclusion Criteria:
- Past 30-day persistent pain
- Cardiovascular or circulatory disorders
- Diabetes
- Current pregnancy
- Open sores/frostbite on nondominant hand
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Exclusion by White "Players"
Excluded by White "players" in an online ball-tossing game (Cyberball).
|
|
|
No Intervention: Inclusion by White "Players"
Included by White "players" in an online ball-tossing game (Cyberball).
|
|
|
Experimental: Exclusion by White "Players" with Bystander Acknowledgment
Excluded by White "players" in an online ball-tossing game (Cyberball) with a White bystander acknowledging the exclusion.
|
The experimenter said "That is so messed up that they excluded you in the task.
And honestly, I would say it was racist…" acknowledgment of the participants experience, "…this shouldn't have happened, and I'm really sorry it did…" an apology, and "…I'm going to talk to the primary investigators of the study to figure out how we can make sure that this won't happen to other people" a plan of action.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Threshold measured with a cold pressor task
Time Frame: Measured immediately after the manipulation (within minutes).
|
Time (in seconds) from the participant places their hand in cold water, to telling the experimenter they are experiencing pain.
|
Measured immediately after the manipulation (within minutes).
|
|
Pain Tolerance
Time Frame: Measured immediately after the manipulation (within minutes).
|
Time (in seconds) from the participant places their hand in cold water, to when they remove their hand from the water.
|
Measured immediately after the manipulation (within minutes).
|
|
Pain unpleasantness
Time Frame: Measured immediately after the manipulation (within minutes).
|
Measured with a the McGill-Pain Questionnaire Short Form, the degree of unpleasantness the participant reports from the pain.
|
Measured immediately after the manipulation (within minutes).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Psychological Needs Satisfaction; Self Control subscale
Time Frame: Measured immediately after the manipulation (within minutes).
|
Needs-Satisfaction Scale (Zadro et al., 2004)
|
Measured immediately after the manipulation (within minutes).
|
|
Psychological Needs Satisfaction; Belongingness subscale
Time Frame: Measured immediately after the manipulation (within minutes).
|
Needs-Satisfaction Scale (Zadro et al., 2004)
|
Measured immediately after the manipulation (within minutes).
|
|
Psychological Needs Satisfaction; Meaningful Existence subscale
Time Frame: Measured immediately after the manipulation (within minutes).
|
Needs-Satisfaction Scale (Zadro et al., 2004)
|
Measured immediately after the manipulation (within minutes).
|
|
Psychological Needs Satisfaction; Self esteem subscale
Time Frame: Measured immediately after the manipulation (within minutes).
|
Needs-Satisfaction Scale (Zadro et al., 2004)
|
Measured immediately after the manipulation (within minutes).
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2022
Primary Completion (Actual)
January 31, 2023
Study Completion (Actual)
January 31, 2023
Study Registration Dates
First Submitted
October 23, 2023
First Submitted That Met QC Criteria
October 27, 2023
First Posted (Actual)
November 2, 2023
Study Record Updates
Last Update Posted (Actual)
November 2, 2023
Last Update Submitted That Met QC Criteria
October 27, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 224125
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
Shared data will be available on OSF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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