Confidence, SelfNCT07559383
Confidence in Students Participation in a Planned Mass Casualty Event
An observational study of Confidence, Self, run by Youngstown State University at 1 site in United States.
Trial summary
The purpose of this study is to determine students' perceptions of and following a planned mass casualty simulation. Primary Aim: To determine students' perceptions on teamwork, communication, confidence, and what students learned. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Confidence, Self
- What is being tested?
- Survey using a questionnaire.
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 200 participants
- Where
- 1 siteUnited States
- Study dates
- 24 Apr 2026to 24 Apr 2026
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Current YSU students who have expressed a willingness to participate in the planned mass casualty simulation
Who may be able to join
- Current YSU students who have expressed a willingness to participate in the planned mass casualty simulation
- Age 18 years or older
- Willing to participate in the study
Who cannot join
- ge less than 18 years
- Not enrolled at Youngstown State University
- Unwilling to participate
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Mass Casualty Event
The purpose of this study is to determine students' perceptions of and following a planned mass casualty simulation.
Primary Aim: To determine students' perceptions on teamwork, communication, confidence, and what students learned.
Read the detailed description
Pre-Survey Before Simulation:
- Students who consent to participate will complete the survey before the planned mass casualty simulation.
- Survey includes basic demographic information (age, gender, race/ethnicity, discipline)
- Survey includes five questions about student confidence prior to the simulation.
- Estimated completion time: 5 minutes
Post-Survey (After Simulation):
- After completing the planned mass casualty session, students will complete the attached post simulation survey via Microsoft forms
- Estimated completion time: 5 minutes
Debrief Post Simulation Students who will be broken up into groups of 10 and asked the following debriefing questions. All students will be asked to participate in the debrief as part of the planned mass casualty simulation. There is no grading attached to the debrief for any student. Their responses will be recorded and de-identified. Students may leave at any time. The attached debrief questions (created by the researchers) will be asked by the faculty participating in the planned mass casualty event. Estimated completion time 20-30 minutes.
- Conditions
- Confidence, Self
- Being tested
- Survey using a questionnaire.
- Keywords
- Planned Mass Casualty Event, Student Confidence
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Survey using a questionnaire.Behavioural
Also called Debrief
Post survey
| Study group | Role | What they receive |
|---|---|---|
| Students | YSU Students Receives: Behavioral: Survey using a questionnaire. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Survey
The purpose of this study is to determine students' perceptions of and following a planned mass casualty simulation.
Measured: 24 hours
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Apr 2026
- Study start24 Apr 2026
- Primary completion24 Apr 2026
- Study completion24 Apr 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Confidence, SelfStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Youngstown State University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Nancy Landgraft, Youngstown State University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07559383
- Sponsor's protocol ID
- 2026-251
- Status last verified
- Apr 2026
- First submitted
- 23 Apr 2026
- Last updated
- 30 Apr 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: Still working through this
Study at a glance
From the registry record, last updated by the sponsor on 30 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Mass Casualty Event
- ClinicalTrials.gov ID
- NCT07559383
- Acronym / sponsor ID
- 2026-251
- Conditions
- Confidence, Self
- Keywords
- Planned Mass Casualty Event, Student Confidence
- Study type
- Observational
- Recruitment status
- Active, not recruiting
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- Youngstown State UniversityUniversity, hospital or other
- Study start
- 24 Apr 2026 (actual)
- Primary completion
- 24 Apr 2026 (actual)
- Study completion
- 24 Apr 2026 (estimated)
- First posted
- 30 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to determine students' perceptions of and following a planned mass casualty simulation.
Primary Aim: To determine students' perceptions on teamwork, communication, confidence, and what students learned.
Detailed description
Pre-Survey Before Simulation:
- Students who consent to participate will complete the survey before the planned mass casualty simulation.
- Survey includes basic demographic information (age, gender, race/ethnicity, discipline)
- Survey includes five questions about student confidence prior to the simulation.
- Estimated completion time: 5 minutes
Post-Survey (After Simulation):
- After completing the planned mass casualty session, students will complete the attached post simulation survey via Microsoft forms
- Estimated completion time: 5 minutes
Debrief Post Simulation Students who will be broken up into groups of 10 and asked the following debriefing questions. All students will be asked to participate in the debrief as part of the planned mass casualty simulation. There is no grading attached to the debrief for any student. Their responses will be recorded and de-identified. Students may leave at any time. The attached debrief questions (created by the researchers) will be asked by the faculty participating in the planned mass casualty event. Estimated completion time 20-30 minutes.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Students | – | Behavioral: Survey using a questionnaire.YSU Students |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Current YSU students who have expressed a willingness to participate in the planned mass casualty simulation
Key inclusion criteria (3 listed)
- Current YSU students who have expressed a willingness to participate in the planned mass casualty simulation
Key exclusion criteria (3 listed)
- ge less than 18 years
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Survey using a questionnaire.Also: DebriefPost survey | Behavioural | Students |
Primary outcome
Survey
Time frame: 24 hours
The purpose of this study is to determine students' perceptions of and following a planned mass casualty simulation.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Apr 2026.
- Individual participant dataSharing planned: Undecided. Still working through this
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Confidence, Self, run by Youngstown State University at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 30 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Survey (time frame: 24 hours). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Apr 2026.