Clinical trial

Role Of Sensitivity to neuroEndocrine Systems in Social Decisions

Name
22-1839
Description
The purpose of this research study is to investigate how personality traits and neuroendocrine systems relate to decision-making patterns in individuals 18-45 years old. The main question it aims to answer is how neuroendocrine activity impacts decision-making. This study has two components. First, there will be an online session that participants complete to consent into the study, complete self-report surveys and a cognitive assessment, and confirm their eligibility for the second part of the study. If eligible to continue, participants will complete one in-person experiment session, during which they will complete self-report measures and a decision-making task. During the in-person session, participants will be randomly assigned (like flipping a coin) to ingest either a placebo (non-active) or the combination of hydrocortisone and yohimbine.
Trial arms
Trial start
2024-07-01
Estimated PCD
2025-07-01
Trial end
2025-07-01
Status
Withdrawn
Phase
Early phase I
Treatment
Hydrocortisone
Hydrocortisone 20 mg capsule will be administered orally.
Arms:
Hydrocortisone + Yohimbine
Other names:
Cortef
Yohimbine
Yohimbine 20 mg capsule will be administered orally.
Arms:
Hydrocortisone + Yohimbine
Other names:
Yohimbine Hydrochloride
Placebo
Two placebos will be administered orally.
Arms:
Placebo + Placebo
Other names:
Sugar pill
Primary endpoint
Goal-directed decision-making in the Social Decision Tree Task (SDTT)
Collected for 30 minutes ~1 hour into Session 2, which takes place on approximately Day 7 of the study
Change in salivary cortisol
Collected immediately before the drug/placebo administration (~5 minutes into the session) and 45 minutes after the drug/placebo administration (~50 minutes into the session) in Session 2, which takes place on approximately Day 7
Pupil diameter during SDTT
Collected for 30 minutes ~1 hour into Session 2, which takes place on approximately Day 7 of the study
Eligibility criteria
Inclusion Criteria: Borderline Personality Disorder (BPD) group: * Score of 38 or higher on PAI-BOR * Participants in the BPD group will be primarily recruited from the two DEPENd lab studies that maintain large samples of BPD participants. To ensure maximal similarity between BPD participants recruited from other DEPENd lab studies and BPD participants recruited through other recruitment sources, the investigators will use the same criteria for the BPD group in the ROSES study as the criteria used in the other DEPENd lab studies. BPD participants in the two DEPENd lab studies from which the investigators will be recruiting must meet the following criteria: 1. 3+ BPD symptoms, one of which must be affective instability, per clinical interview 2. Participants must score at least 80 on the Reynolds Intellectual Screening Test (RIST). Matched Control (MC) group: * Score of 12 or lower on PAI-BOR * Score below 50th percentile on WHODAS Combined Inclusion Criteria: * Ages 18-45 * Provision of signed and dated informed consent form * Stated willingness to comply with all study procedures and lifestyle considerations and availability for the duration of the study * Willingness to participate in all components of the study * Access to necessary resources for participating in the virtual Session 1 (i.e., computer, smartphone, internet access) * Participants must be able to speak, understand and read English. * Participants must have at least 20/40 visual acuity (correct or uncorrected). Exclusion Criteria: * Current use of medications that interact adversely with yohimbine a. Iobenguane radiopharmaceutical products * Current use of medications that interact adversely with hydrocortisone 1. Aldesleukin 2. Bacillus Calmette-Guérin (BCG) Products 3. Cladribine 4. Dengue Tetravalent Vaccine 5. Desmopressin 6. Indium 111 Capromab Pendetide 7. Macimorelin 8. Mifamurtide 9. MiFEPRIStone 10. Natalizumab 11. Pimecrolimus: 12. Ruxolitinib (Topical) 13. Tacrolimus (Topical) 14. Talimogene Laherparepvec 15. Tertomotide 16. Phenytoin 17. Rifampin 18. Troleandomycin 19. Ketoconazole 20. High-dose aspirin (\>30 mg/kg/day) * Contraindicated medical conditions of yohimbine 1. Renal dysfunction 2. Hepatic dysfunction 3. Heart failure 4. Psychotic Disorder or psychosis 5. Hypotension 6. Diabetes 7. Heart disease 8. Kidney disease 9. Liver disease 10. Nervous disorder 11. Gastric ulcer 12. Duodenal ulcer * Contraindicated medical conditions of hydrocortisone 1. Hypersensitivity to hydrocortisone or any component of the formulation 2. Systemic fungal infections 3. Latent Tuberculosis, Tuberculosis reactivity, active Tuberculosis 4. Cardiovascular disease 5. Diabetes 6. Gastrointestinal diseases i. Diverticulitis ii. Fresh intestinal anastomoses iii. Active or latent peptic ulcer iv. Ulcerative colitis v. Abscess vi. Renal insufficiency vii. Other pyogenic infection g. Hepatic impairment h. Kidney impairment i. Myasthenia gravis j. Osteoporosis k. Pheochromocytoma l. Seizure disorders m. Septic shock or sepsis syndrome n. Systemic sclerosis o. Thyroid disease p. Strongyloides (threadworm) infestation q. Ocular herpes simplex r. Hypertension * Given a live vaccine within 2 weeks of completing Visit 1. Recent administration of the following vaccines are specifically contraindicated for hydrocortisone: 1. Typhoid Vaccine 2. Yellow Fever Vaccine 3. Poliovirus Vaccine (Live/Trivalent/Oral) 4. Rubella- or Varicella-Containing Live Vaccines * Have a current infection * Pregnancy * Individuals lactating * Recent antihypertensive agents * History of psychotic disorder, Bipolar I disorder, autism spectrum disorder, reactive attachment disorder, pervasive developmental disorder, motor disorder, head injury, mental retardation, neurological disorder, or current substance dependence * Family history of Bipolar I disorder in a first degree relative.
Protocol
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Updated at
2024-06-05

1 organization

1 product

1 drug

1 indication