Un modelo de proceso multinomial de juicio moral (PSY)
The main goal of this project to investigate the psychological processes underlying moral judgments in social dilemmas. We will examine neuroendocrine determinants of moral judgment by investigating the effects of exogenous testosterone
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
- Medical Screening Interview: Participants will be asked to answer several questions to identify potential medical and non-medical conditions that would preclude the self-administration of testosterone.
- First Saliva Sample: Participants will be asked provide a saliva sample after they completed the medical screening interview.
- Testosterone Self-Administration: Immediately following the first saliva collection, participants will self-administer spray puffs of either testosterone or placebo.
- Relaxation: Participants will be given the opportunity to relax for 30 minutes.
- Moral Dilemmas Judgments: Participants will be asked to read a set of 24 moral dilemmas that describe situations in which an actor has to make a decision on whether or not to engage in a particular action (e.g., sacrifice the well-being of one person to protect the well-being of several others). Participants will be asked to indicate whether they consider the described action acceptable or unacceptable.
- Demographics: Participants will be asked to indicate their gender, age, and ethnicity.
- Ear Temperature, heart rate, and blood pressure will be measured before drug administration, and again 20 minutes after drug administration. If temperature changes more than 2 degrees, heart rate changes more than 20bmp, or if blood pressure changes more than 20%, the experiment will be terminated and subjects will be escorted across the street to the University Emergency Room.
Tipo de estudio
Inscripción (Actual)
Fase
- Fase 4
Contactos y Ubicaciones
Ubicaciones de estudio
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Texas
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Austin, Texas, Estados Unidos, 78712
- University of Texas at Austin Department of Psychology
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- must be currently enrolled at The University of Texas at Austin
Exclusion Criteria:
- not comfortable with the self-administration of testosterone for the purpose of our study less than 18 years old BMI less than 18 or above 27 suffer from any of the physical health conditions listed on the pre-screen questionnaire (I will not ask about mental health because our study is not about mental health) take any of the medications listed on the pre-screen questionnaire currently pregnant (females) irregular cycle in the past 6 months (females) smoke more than 5 cigarettes/day use cocaine more than once/month (**or should I exclude all those who use any drugs recreationally more than once/month?**) drink more than 10 alcoholic beverages/week
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Ciencia básica
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Triple
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Testosterone
14mg testosterone will be administered intranasally in a 1milliliter aqueous solution |
Effect of testosterone on moral decision making |
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Comparador de placebos: Placebo
1ml blank (containing no drug) aqueous solution will be administered intranasally |
Effect of testosterone on moral decision making |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Probability of Making a Moral Judgment That Aligns With Moral Norms
Periodo de tiempo: 90 minutes
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Participants were asked to read and respond to a validated set of 24 moral dilemmas. The dilemma set included 4 parallel versions of 6 basic scenarios that varied in terms of whether (a) the dilemma involved a proscriptive norm that prohibits action or a prescriptive norm that prescribes action and (b) the benefits of the described action for overall well-being are either greater or smaller than its costs for overall well-being. Participants were asked to indicate for each dilemma whether or not they would perform the described action, using forced-choice options labeled yes and no. |
90 minutes
|
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Probability of Making a Moral Judgment That Maximizes Welfare
Periodo de tiempo: 90 minutes
|
Participants were asked to read and respond to a validated set of 24 moral dilemmas. The dilemma set included 4 parallel versions of 6 basic scenarios that varied in terms of whether (a) the dilemma involved a proscriptive norm that prohibits action or a prescriptive norm that prescribes action and (b) the benefits of the described action for overall well-being are either greater or smaller than its costs for overall well-being. Participants were asked to indicate for each dilemma whether or not they would perform the described action, using forced-choice options labeled yes and no. |
90 minutes
|
|
Probability of Making a Moral Judgment That Involves Inaction Versus Action
Periodo de tiempo: 90 minutes
|
Participants were asked to read and respond to a validated set of 24 moral dilemmas. The dilemma set included 4 parallel versions of 6 basic scenarios that varied in terms of whether (a) the dilemma involved a proscriptive norm that prohibits action or a prescriptive norm that prescribes action and (b) the benefits of the described action for overall well-being are either greater or smaller than its costs for overall well-being. Participants were asked to indicate for each dilemma whether or not they would perform the described action, using forced-choice options labeled yes and no. |
90 minutes
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Robert A Josephs, PhD, Professor
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimado)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2014-12-0010
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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