Social Stress Clinical Trial
— SSBIOfficial title:
Investigating the Effects of Social Stress on Brain Imaging
The purpose of this study is to examine whether experiencing a social stressor prior to the collection of neuroimaging measures is associated with differences in brain activation in healthy participants.
Status | Not yet recruiting |
Enrollment | 50 |
Est. completion date | May 2025 |
Est. primary completion date | December 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 55 Years |
Eligibility | Inclusion Criteria: - Ability and willingness to provide written informed consent. - Sufficiently fluent in English to participate in the trial. - Between 18-55 years of age (inclusive). - Right-hand dominant. - Current medications are stable for past 30 days (no changes to dose or frequency). - Negative result on pregnancy test (if female). - Negative result on urine drug screening. - No clinically significant mental health disorders (QuickSCID-5). - Liebowitz Social Anxiety Scale (LSAS <30). Exclusion Criteria: - History of bipolar disorder, schizophrenia, psychosis, delusional disorders. - History of eating disorder within past 6 months. - History of any traumatic brain injury. - Currently diagnosed with diabetes mellitus. - Presence of severe medical illness that would prevent completion of study procedures. - Presence of significant neurological illness or cognitive dysfunction (e.g.; seizures, dementia). - History of substance use disorder within past 6 months (other than nicotine and caffeine). - Use of any cannabis-containing products in past 30 days (CBD or THC). - Use of beta-blockers or benzodiazepines in past 2 weeks. - History of claustrophobia. - Contraindications for MRI (e.g.; shrapnel). - Presence of any other medical condition that, in the investigator's opinion, may interfere with the study procedures. |
Country | Name | City | State |
---|---|---|---|
United States | Massachusetts General Hospital | Boston | Massachusetts |
United States | Massachusetts Institute of Technology | Cambridge | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Massachusetts Institute of Technology | Massachusetts General Hospital |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Differences in fMRI BOLD Response | Patterns of brain activation measured as blood-oxygenation-level dependent (BOLD) signals will be assessed using 3.0 Tesla (3T) functional magnetic resonance imaging (fMRI). Several exploratory imaging paradigms, including the emotional face-matching task (EFMT) and the self-referential comment task (SRCT), will be used to examine differences between participants who experience the TSST and those who do not. | Day 1 |
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