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Active, not recruitingNCT07885670Updated Oct 22, 2026

Comparing the Effect of Scenario-Based Teaching Method to Conventional Method on Medical Students' Knowledge and Satisfaction in Psychiatry Interns

An interventional study of scenario-based teaching method in Knowledge and Satisfaction, sponsored by Mashhad University of Medical Sciences. Active, not recruiting at 1 site in Iran. Per ClinicalTrials.gov, last updated 2026-10-22.

Sponsored by Mashhad University of Medical Sciences · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 10 months after the study started (first participant enrolled Oct 2025, registered Sep 2026).
Updated Oct 21, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
132
Allocation
Not applicable
Sex
All
01

Study summary

Traditional medical education methods, which rely heavily on lectures and textbook study, have come under criticism for their inability to foster the critical thinking, clinical reasoning, and practical skills required to manage complex psychiatric cases. The static nature of these methods fails to replicate the dynamic and unpredictable scenarios of real-world clinical practice, thereby hindering students' preparedness for the multifaceted challenges of psychiatric care However, across various disciplines-particularly in medical and allied health sciences-new methods emphasizing active student participation have gained prominence. One such modern approach in health sciences education is scenario-based learning; grounded in situated learning theory, it brings students closer to the professional realities of their field. This method utilizes scenarios as tools for teaching and learning, enabling students to learn from real-world experiences and apply them in practice.

02

Conditions studied

  • Knowledge
  • Satisfaction

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Keywords

  • scenario-based teaching
  • psychiatry internship
  • knowledge
  • satisfaction
03

In context

Personal Satisfaction

143 studies on the registry are indexed under Personal Satisfaction; 50 are open to participants now.

This study's planned enrollment of 132 is above the median of 90 across 119 interventional studies indexed under Personal Satisfaction.

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Lead sponsor

Mashhad University of Medical Sciences is the lead sponsor of 92 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

intern of psychiatry, tendency to participate in study

Exclusion criteria

Exclusion Criteria:

history of participating in similar course in psychiatry, severe health problems leading to leave the course, incomplete data collection forms, not following the study

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
132 participants (estimated)

Study arms

  • Experimental
    psychiatry interns who receive scenario-based teaching method

    Two 90-minute sessions of scenario-based training utilizing real-life psychiatric case scenarios. Each session focuses on a specific psychiatric disorder or clinical scenario, with sufficient time allocated for discussion and feedback.

    Other: scenario-based teaching method

Interventions

  • Otherscenario-based teaching method

    Two 90-minute sessions of scenario-based training utilizing real-life psychiatric case scenarios. Each session focuses on a specific psychiatric disorder or clinical scenario, with sufficient time allocated for discussion and feedback.

06

What researchers measure

Primary outcomes

  1. knowledge and satisfaction

    knowledge will be tested using written MCQ exams. Its Cut off point will be 14 out of 20. and satisfaction will be tested through a Likert- scale tool whose psychometrics have been confirmed It consists of 10 questions designed using a 5-point Likert scale (ranging from "very poor" = 1 to "very good" = 5). The scoring range will be 1 to 5, and the minimum acceptable score for the satisfaction level is 4 (equivalent to 75% satisfaction).

    Time frame: knowledge will be measured both at baseline, the first day of entering to psychiatry department and at the last day of the psychiatry course. satisfaction will be tested at the last day of the course for average two years.

  2. knowledge and satisfaction

    knowlege will be tested using written tests based on scenarios and satisfaction will be tested via an likert-scale inventory whose psychometric properties have been confirmed

    Time frame: knowledge will be measured both at baseline, the first day of entering to psychiatry department and at the last day of the psychiatry course. satisfaction will be tested at the last day of the course for average two years

07

Study locations

1 site
  • Mashhad University of Medical Sciences
    Mashhad, Razavi Khorasan Province, Iran
08

References and documents

Individual participant data

Plan to share: No — The scores are confidential because they are recorded in the students' educational files and saved in personally

No publications or documents are linked to this record.

09

Updates

2 registry updates since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 21, 2026
Show all 2 updates
  1. Oct 22, 2026
    Minor edits only
    + 1 other change: identifiers
  2. Oct 21, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07885670
Lead sponsor
Mashhad University of Medical Sciences
Responsible party
nazila zarghi (Head of research in medical education unit, Education Development Center, Mashhad University of Medical Sciences) — Principal investigator
First posted
Oct 21, 2026
Start date
Oct 21, 2025
Primary completion
Aug 31, 2026
Completion
Oct 31, 2026 (estimated)
Last update
Oct 22, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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