Moral Reasoning Intervention on Moral Justification Abilities

December 16, 2025 updated by: Prof. Massimo Filippi, IRCCS San Raffaele

Effects of a Moral Reasoning Intervention on Moral Justification Abilities

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.

Study Overview

Detailed Description

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.

Study Type

Interventional

Enrollment (Actual)

86

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Italy
      • Milan, Italy, Italy, 20132
        • IRCCS San Raffaele

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • University students (other than Philosophy) within the first 3 years
  • Aged between 18 and 26 years old
  • Italian speakers
  • Oral and written informed consent to study participation

Exclusion Criteria:

  • A current psychiatric condition
  • Contraindications to MRI study (cardiac pacemakers; metal splinters or fragments; metal protheses not compatible with the magnetic field; claustrophobia; women who are pregnant or intending to become pregnant during the study; breastfeeding women).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Moral
The Moral group will read a short text explaining the meaning and function of moral justification, and outlining brief descriptions of six morally relevant factors. The Moral group will then attend a 1h30 lecture on moral reasoning.
One and a half-hour long lecture on moral justification and moral reasoning
Active Comparator: Non-moral
The Non-moral will read a short text explaining the meaning and function of argumentation, and outlining brief descriptions of six logical and argumentative principles. The Non-moral group will then attend a 1h30 lecture on (non-moral) logical reasoning.
One and a half-hour long lecture on logical and argumentative principles

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Short and mid-term (one month) impact of moral vs non-moral reasoning interventions on moral justification abilities in non-expert subjects when performing a moral dilemma.
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.
Baseline, 5 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Relationship between brain BOLD activity during task-based fMRI and changes in moral justification abilities.
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.
Baseline, 5 weeks
Relationship between brain BOLD activity during task-based fMRI and agreement with moral statements.
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.
Baseline, 5 weeks
Relationship between brain BOLD activity during task-based fMRI and confidence post-intervention.
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.
Baseline, 5 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 18, 2022

Primary Completion (Actual)

February 19, 2024

Study Completion (Actual)

October 13, 2025

Study Registration Dates

First Submitted

July 31, 2024

First Submitted That Met QC Criteria

December 13, 2024

First Posted (Actual)

December 16, 2024

Study Record Updates

Last Update Posted (Actual)

December 23, 2025

Last Update Submitted That Met QC Criteria

December 16, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • Moral-REA

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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