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Can a 20-Minute video make teens Disaster-Ready?

NCT ID NCT07781527

Prevention Sponsor: Tanjungpura University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 24, 2026 · Last updated Aug 25, 2026 · Updated 1 time

Summary

This trial tests whether a short, purpose-built educational video can strengthen high-school students' belief in disaster preparedness and their perception of disaster risk. About 144 students from twelve classes at one school in West Kalimantan, Indonesia, will be randomly assigned to watch either the disaster-education video or a general health video. Questionnaires measure changes in risk perception and preparedness belief right after the session and again four weeks later.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Audiovisual disaster-education module (a 20-minute educational video on disaster preparedness)
What this could lead to
If effective, this video could become a simple, scalable tool to help young people in disaster-prone areas better understand risks and feel more prepared to act.
What could go wrong
This is a small, early-stage trial in a single school, so results may not apply broadly. The video aims to change beliefs and perceptions, not actual disaster outcomes, and its effects may fade over time.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 144 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Jan 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

15 to 19 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Cluster (class) level: \- Intact class of grade X, XI, or XII within the participating school Individual (student) level: * Actively enrolled student in grade X, XI, or XII * Present on the scheduled data-collection and intervention days * Written informed consent provided by a parent or legal guardian, and written assent provided by the adolescent * Able to view the full audiovisual session and complete the study questionnaires Exclusion Criteria: Cluster (class) level: \- Class unavailable for the full schedule of sessions during the study window (for example, examination or fieldwork commitments) Individual (student) level: * Acute illness preventing participation on the study day * Withdrawal of adolescent assent or guardian consent at any point * Unable to complete the intervention session (for example, must leave before the video ends); such records are retained for the intention-to-treat analysis but flagged for the per-protocol set

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Conditions

The condition(s) this trial relates to.

Adolescent Behavior Health Behavior Health Education pemphigus and fogo selvagem

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Adolescent behavior Disaster preparedness Disasters Health behavior Health education Risk perception

How to take part

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  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  2. A doctor treating you

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