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Does being treated unfairly keep you up at night? study says yes.
NCT ID NCT03937973
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how race-based social rejection impacts sleep and nighttime heart function. About 139 African American and Caucasian adults spent two nights in a sleep lab—one after a rejection task and one after a neutral task. Researchers measured how quickly they fell asleep and how well they slept using brain-wave monitoring.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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139 people
The number who actually took part.
- Started
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Apr 2019
- Finished
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May 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 64 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age: 18 to 64 years old * Self-identified as African American/Black or Caucasian American/White * English speaking, able to provide consent * Self-reported bedtime between 10PM and 12AM for 5/7 nights for the past 3 months (stability to be confirmed by sleep diary and wrist actigraphy). * Self-reported sleep duration between 6.5 and 8.5 hours for 5/7 nights for the last month (duration to be confirmed by actigraphy and sleep diary) Exclusion Criteria: * Body mass index of 40 or above * Participants at high risk for obstructive sleep apnea, based on "high risk" score from the STOP-Bang. * Medical or psychiatric condition, as assessed by self-report and clinical interview that affect sleep and/or cardiovascular functioning, including doctor diagnosed arrhythmia, hypertension, congestive heart failure, major depression, bipolar disorder, post-traumatic stress disorder. * Medication use that is likely to affect sleep and/or cardiovascular functioning, including antidepressants, anxiolytic or soporific medication, and beta-blockers.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of California, San Francisco
San Francisco, California, 94118, United States
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Other studies related to the condition(s) this trial covers.
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