IRCCS San Raffaele
Milan, Italy, 20132
NCT Number: NCT06735989
The primary aim of this study is to evaluate the short (immediate) and mid-term (one month) impact of moral (vs non-moral) reasoning interventions on the moral justification abilities in non-expert subjects. Such an impact will be assessed by observing quantitative changes (on 1 to 4 points scale) of qualitative variables in the moral justification expressed by the subjects.
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Notify Me18 year–26 year
All sexes
Interventional
Not applicable
Milan, Italy, 20132
The aim of this study is to test wether a single intervention on moral reasoning can have short and/or mid-term effects on the justification of moral judgements about a problematic moral case. Focusing on justification allows to assess reasonable improvement by referring to a procedural standard, that is, without assuming any substantive normative view; namely, without evaluating a "betterment" on the basis of the content of moral judgements, but rather on the satisfaction of formal, procedural conditions in their justification. Our standard for a good moral justification consists in a set of procedural features, such as logical, empirical, and conceptual competence, openness to revision, sympathetic imagination, and bias avoidance.
Once enrolled, participants will be randomized through random.org software in the two experimental groups: 1) the moral and 2) the non-moral condition. Allocation concealment will be carried out through closed and opaque mails by a blind operator. Subjects will undergo a neuropsychological assessment and a (optional) task-based fMRI at study entry. Furthermore, during the day of the intervention (seminar: moral or logical reasoning), participants will undergo a pre-test (before the intervention) and a post-test (after the intervention) on a morally problematic case. The same test will be repeated by all participants one month after the intervention.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
One and a half-hour long lecture on moral justification and moral reasoning
One and a half-hour long lecture on logical and argumentative principles
Time frame: Baseline, 5 weeks
The primary aim of this study is to evaluate the short (immediate) and mid-term (one month) impact of moral (vs non-moral) reasoning interventions on the moral justification abilities in non-expert subjects. Such an impact will be assessed by observing quantitative changes (on a 0 to 3 points scale) in the moral justifications expressed by the subjects in six domains: empirical competence, conceptual competence, logical coherence, sympathetic imagination, bias reduction, openness to revision of opinions.
Time frame: Baseline, 5 weeks
To investigate the relationship between pre-intervention subjects' brain BOLD activity during a task-based functional MRI (fMRI), using a moral reasoning paradigm, and changes in moral justification abilities in six domains (empirical competence, conceptual competence, logical coherence, sympathetic imagination, bias reduction, openness to revision of opinions) assessed using a 0-3 point scale.
Time frame: Baseline, 5 weeks
To investigate the relationship between pre-intervention subjects' brain BOLD activity during a task-based functional MRI (fMRI), using a moral reasoning paradigm, and agreement with moral statements assessed using a 0-3 point scale.
Time frame: Baseline, 5 weeks
To investigate the relationship between pre-intervention subjects' brain BOLD activity during a task-based functional MRI (fMRI), using a moral reasoning paradigm, and confidence post-intervention assessed by using 0-3 point scales.
IRCCS San Raffaele
Other
Effects of a Moral Reasoning Intervention on Moral Justification Abilities
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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