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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06113926
Other study ID # 224125
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2022
Est. completion date January 31, 2023

Study information

Verified date October 2023
Source George Washington University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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).


Recruitment information / eligibility

Status Completed
Enrollment 92
Est. completion date January 31, 2023
Est. primary completion date January 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Bystander Acknowledgment
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.

Locations

Country Name City State
United States The George Washington University Washington District of Columbia

Sponsors (4)

Lead Sponsor Collaborator
George Washington University D.C. Psychological Association, Psi Chi, Society for the Psychological Study of Social Issues

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Threshold measured with a cold pressor task 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).
Primary Pain Tolerance 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).
Primary Pain unpleasantness 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 Psychological Needs Satisfaction; Self Control subscale Needs-Satisfaction Scale (Zadro et al., 2004) Measured immediately after the manipulation (within minutes).
Secondary Psychological Needs Satisfaction; Belongingness subscale Needs-Satisfaction Scale (Zadro et al., 2004) Measured immediately after the manipulation (within minutes).
Secondary Psychological Needs Satisfaction; Meaningful Existence subscale Needs-Satisfaction Scale (Zadro et al., 2004) Measured immediately after the manipulation (within minutes).
Secondary Psychological Needs Satisfaction; Self esteem subscale Needs-Satisfaction Scale (Zadro et al., 2004) Measured immediately after the manipulation (within minutes).
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