DisastersDERAPNCT07781527
Effectiveness of an Audiovisual Disaster-Education Intervention on Disaster Risk Perception and Preparedness Belief Among Senior High-School Adolescents
A study testing Audiovisual disaster-education module and Attention-matched general-health video in people with Disasters and Disaster Preparedness, run by Tanjungpura University.
Trial summary
This cluster-randomized controlled trial tests whether a short, standardized disaster-education video improves two psychological precursors of disaster preparedness among senior high-school students in a hazard-prone district of West Kalimantan, Indonesia. Read more about this study
- Who is it for?
- Ages 15 to 19 yearsHealthy volunteers can take part
- Conditions the study is for
- Disasters, Disaster Preparedness, Health Behavior
- What is being tested?
- Audiovisual disaster-education module and Attention-matched general-health video
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 144 participants
- Where
- No sites listed yet
- Study dates
- 15 Oct 2026to 20 Jan 2027
- Phase
- Interventional
- 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 15 to 19 years
- All sexes
- Healthy volunteers accepted
- Child, Adult
Who may be able to join
- 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
Who cannot join
- 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
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
I Made Moh. Yanuar Saifudin, S.Kep., Ns., M.Kep. contact
About this study
Official title: Effectiveness of an Audiovisual Disaster-Education Intervention on Disaster Risk Perception and Preparedness Belief Among Senior High-School Adolescents in West Kalimantan, Indonesia
This cluster-randomized controlled trial tests whether a short, standardized disaster-education video improves two psychological precursors of disaster preparedness among senior high-school students in a hazard-prone district of West Kalimantan, Indonesia.
Twelve intact classes at one senior high school will be randomized 1:1, stratified by grade level, either to view a purpose-built audiovisual disaster-education module (approximately 20 minutes, shown twice in a single classroom session) or to view an attention-matched general adolescent-health video of similar length on an unrelated topic. Randomization is at the class level to reduce contamination between students, and the individual student is the unit of analysis. All students in a participating class view the video allocated to that class; a randomly drawn subsample of twelve students per class, 144 in total, completes the study questionnaires.
Read more
Two co-primary outcomes are measured in every participant. The first is disaster preparedness belief, measured by the General Disaster Preparedness Belief (GDPB) scale. The second is disaster risk perception, measured by the Disaster Risk Perception Scale (DRPS). Both are collected at baseline before allocation, immediately after the session, and again four weeks later.
The intervention and both instruments are grounded in the Health Belief Model, which predicts that raising perceived threat contributes to readiness to act. An exploratory mediation analysis will test whether change in risk perception explains part of any effect on preparedness belief.
After the four-week assessment, control classes are offered the full disaster-education intervention.
Read the detailed description
Background. West Kalimantan, including Kubu Raya Regency, is exposed to recurrent seasonal flooding and to land and forest fires with associated haze. Adolescents are rarely the explicit target of preparedness interventions despite being reachable at scale through schools, capable of transmitting preparedness knowledge within households, and themselves vulnerable during emergencies. Audiovisual media engage sight and hearing simultaneously, simplify complex content, and standardize delivery, making a short video a plausible low-cost vehicle for shifting the cognitive precursors of preparedness behavior.
Theoretical framework. The intervention is grounded in the Health Belief Model (HBM). Disaster risk perception corresponds to the upstream perceived-threat component of the HBM, comprising perceived susceptibility and perceived severity. Disaster preparedness belief captures the fuller, more downstream readiness-to-act constellation, combining threat appraisal with perceived benefits, perceived barriers, self-efficacy, and cues to action. Each content block of the video is mapped a priori to a specific HBM construct and to the outcome subscales it is intended to move, which is the content-validity rationale for using one shared intervention to address both co-primary outcomes.
Design. Two-arm, parallel-group, stratified cluster-randomized controlled trial with 1:1 allocation and a superiority framework. The cluster and unit of randomization is the intact class; the unit of analysis is the individual student. Stratification is by grade level (X, XI, XII), so that within each grade an equal number of classes is assigned to each arm. A computer-generated sequence is produced by the study statistician with the seed recorded. Class identifiers without class names are provided to an independent allocation holder who applies the sequence, giving third-party concealed allocation. Within each eligible class a random subsample of twelve students is drawn from the class roster before any class is randomized, and baseline data are collected from all consented students in that subsample before allocation, so that both participant selection and recruitment are complete before assignment is known. Drawing the subsample before allocation is essential, because selecting participants after clusters have been assigned is the principal source of identification and recruitment bias in cluster trials.
Masking. Participants and facilitators cannot be masked because the intervention is overt. Questionnaires are self-administered and identical across arms. The data manager who enters and cleans the data is masked to allocation, and the statistician conducts the primary analysis on an arm-coded dataset. Unmasking occurs only after the primary analysis is locked.
Sample size. Detecting a moderate standardized difference (Cohen d = 0.50) with two-sided alpha 0.05 and 80 percent power requires approximately 63 students per arm under individual randomization. Because the primary analysis adjusts for the baseline score, this requirement is multiplied by (1 minus r squared), where r is the assumed baseline-to-immediate-post correlation, taken as 0.60, giving approximately 40 students per arm. Twelve intact classes are randomized, six per arm, with twelve students randomly sampled and assessed within each class. The resulting design effect is 1 + (12 minus 1) x 0.05 = 1.55, giving approximately 62 evaluable students per arm. Allowing 15 percent attrition to the four-week follow-up gives an enrollment target of 72 students per arm and 144 in total. All students in participating classes view the assigned video; only the randomly drawn subsample completes the questionnaires. Under these assumptions the trial detects a standardized difference of approximately 0.50 at alpha 0.05, or approximately 0.56 under a Bonferroni-adjusted alpha of 0.025 for a joint co-primary claim. If the true intracluster correlation is 0.02, plausible for attitudinal outcomes, the detectable difference falls to approximately 0.45; if it is 0.10, it rises to approximately 0.59. The mediation analysis is powered only for exploratory purposes at this sample size.
Statistical analysis. For each co-primary outcome the primary analysis is a linear mixed-effects model with a random intercept for class and fixed effects for arm, time, and the arm-by-time interaction, adjusting for the baseline score, the stratification factor (grade), and pre-specified confounders (sex, age, prior personal disaster experience, prior exposure to disaster education). The treatment effect is the adjusted between-arm difference at the immediate post-intervention assessment, reported with a 95 percent confidence interval. Because the sample size claims credit for baseline adjustment, the observed baseline-to-post correlation will be reported alongside the primary result, as will the observed intracluster correlation for each outcome. Generalized estimating equations with an exchangeable working correlation are specified as an equivalent alternative. Baseline balance is described rather than significance-tested, following the Consolidated Standards of Reporting Trials (CONSORT) extension for cluster randomized trials. The primary analysis follows the intention-to-treat principle; a per-protocol analysis is secondary. Missing outcome data are handled by multiple imputation under a missing-at-random assumption with complete-case sensitivity analysis. Each co-primary outcome is tested at two-sided alpha 0.05 within its own analysis, and a Bonferroni-adjusted threshold of 0.025 is applied for any combined family-wise claim. The analysis plan is fixed before unmasking.
Fidelity and contamination. Every session is documented on a fidelity log recording that the correct video was played in full and twice, absence of interruptions or substituted content, adherence to the facilitator script, equipment and room conditions, attendance, and any deviation or contaminating event. Contamination within the single school is mitigated by randomizing at class level, separating data-collection days by arm, and scheduling control assessments so they are not preceded by discussion with intervention classes. Residual contamination is expected to bias effects toward the null.
Post-trial provision. After the four-week assessment, control classes are offered the full audiovisual disaster-education intervention.
- Conditions
- Disasters, Disaster Preparedness, Health Behavior, Risk Perception, Health Education, Adolescent Behavior
- Being tested
- Audiovisual disaster-education module, Attention-matched general-health video
- Keywords
- disaster preparedness, disaster risk perception, Health Belief Model, audiovisual education, adolescents, school-based intervention, cluster randomized trial, Indonesia, West Kalimantan, flood, land and forest fire
- Medical subject headings
- Health Behavior, Health Education, Adolescent Behavior, Pemphigus and fogo selvagem
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Audiovisual disaster-education moduleBehavioural
Also called disaster-education video, DERAP (Disaster Education for Risk-perception And Preparedness) video
A purpose-built educational video on disaster preparedness, approximately 20 minutes in duration, developed through a structured instructional-design cycle (needs analysis, learning objectives, storyboard, production, expert content validation withitem-level content validity index [I-CVI] of at least 0.78 and scale-level content validity index, average method [S-CVI/Ave], of at least 0.90, comprehension pilot, and lock). The defined dose is one viewing repeated twice in the same session, identical for every intervention cluster. An optional fully scripted five-minute debrief may follow. No deviation from this dose is permitted without a documented protocol amendment.
Attention-matched general-health videoBehavioural
Also called Attention control video
A general adolescent-health video on a topic unrelated to disaster preparedness (for example, personal hygiene or balanced nutrition), matched to the experimental module for duration, delivery format, room conditions, and facilitator contact time.
| Study group | Role | What they receive |
|---|---|---|
| Audiovisual disaster-education module | Experimental | Classes allocated to this arm receive, in a single standardized classroom session, a purpose-built audiovisual disaster-education module of approximately 20 minutes, played twice consecutively, optionally followed by a fully scripted five-minute facilitator debrief in which each student names one personal preparedness action. Content blocks cover the definition of disaster, how disasters occur, impacts and risks, benefits of preparedness, personal preparation steps, barriers and misconceptions, social and environmental roles, self-efficacy, environmental knowledge, and a closing call to action, each mapped to a Health Belief Model construct. Delivery is standardized (identical file, equipment, and room set-up) by a trained facilitator following a fixed script and completing a fidelity checklist. Receives: Behavioral: Audiovisual disaster-education module |
| Attention-matched general-health video | Active comparator | Classes allocated to this arm receive, in an equivalent session of similar length and under identical conditions, a general adolescent-health video unrelated to disaster preparedness (for example, on personal hygiene or balanced nutrition). This attention-matched comparator controls for contact time, facilitator attention, and the novelty of receiving a video session, isolating the specific effect of the disaster content. After the four-week follow-up assessment, classes in this arm are offered the full audiovisual disaster-education intervention. Receives: Behavioral: Attention-matched general-health video |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in disaster risk perception, measured by the Disaster Risk Perception Scale total score
Disaster risk perception measured by the Disaster Risk Perception Scale (DRPS), a 25-item instrument covering five dimensions: exposure and impact, probability, uncontrollability, worry and fear, and vulnerability. Each item is scored on a 5-point Likert scale from 1 (strongly disagree) to 5 (strongly agree). The total score is the sum of all 25 items and ranges from a minimum of 25 to a maximum of 125. A higher total score indicates greater perceived disaster risk. Higher scores are not inherently better or worse for health; greater perceived risk is the direction of change the intervention is hypothesized to produce, because perceived threat is the upstream component of the Health Belief Model. The estimand is the between-arm difference in DRPS total score immediately post-intervention, adjusted for the baseline score, grade, and pre-specified confounders, estimated in a linear mixed-effects model with a random intercept for class.
Measured: Baseline (Day 1, pre-intervention) and Day 1, within 30 minutes post-intervention
Change in disaster preparedness belief, measured by the General Disaster Preparedness Belief scale total score
Disaster preparedness belief measured by the General Disaster Preparedness Belief (GDPB) scale, a 38-item instrument based on the Health Belief Model. Each item is scored on a 5-point Likert scale from 1 (strongly disagree) to 5 (strongly agree), with negatively worded items reverse-scored before summation. The total score is the sum of all 38 items and ranges from a minimum of 38 to a maximum of 190. A higher total score indicates stronger disaster preparedness belief, which is the better outcome. The estimand is the between-arm difference in GDPB total score immediately post-intervention, adjusted for the baseline score, grade, and pre-specified confounders, estimated in a linear mixed-effects model with a random intercept for class.
Measured: Baseline (Day 1, pre-intervention) and Day 1, within 30 minutes post-intervention
Secondary outcomes (4)
Retention of effect on disaster preparedness belief at four weeks, measured by the General Disaster Preparedness Belief scale total score
Disaster preparedness belief at the four-week follow-up, measured by the General Disaster Preparedness Belief (GDPB) scale, a 38-item instrument based on the Health Belief Model. Each item is scored on a 5-point Likert scale from 1 (strongly disagree) to 5 (strongly agree), with negatively worded items reverse-scored. The total score ranges from a minimum of 38 to a maximum of 190, and a higher total score indicates stronger disaster preparedness belief, which is the better outcome. The reported value is the adjusted between-arm difference in GDPB total score at four weeks, estimated in the same linear mixed-effects model used for the primary analysis, to assess whether any immediate post-intervention effect on preparedness belief is retained.
Measured: Baseline (Day 1) and Week 4
Retention of effect on disaster risk perception at four weeks, measured by the Disaster Risk Perception Scale total score
Disaster risk perception at the four-week follow-up, measured by the Disaster Risk Perception Scale (DRPS), a 25-item instrument covering exposure and impact, probability, uncontrollability, worry and fear, and vulnerability. Each item is scored on a 5-point Likert scale from 1 (strongly disagree) to 5 (strongly agree). The total score ranges from a minimum of 25 to a maximum of 125, and a higher total score indicates greater perceived disaster risk, which is the direction of change the intervention is hypothesized to produce. The reported value is the adjusted between-arm difference in DRPS total score at four weeks, estimated in the same linear mixed-effects model used for the primary analysis, to assess whether any immediate post-intervention effect on risk perception is retained.
Measured: Baseline (Day 1) and Week 4
General Disaster Preparedness Belief scale subscale scores
Between-arm differences in the six Health Belief Model subscales of the General Disaster Preparedness Belief (GDPB) scale: perceived susceptibility, perceived severity, perceived benefits, perceived barriers, self-efficacy, and cues to action. Because the six subscales contain different numbers of items, each subscale is reported on a common metric as the mean score of its constituent items, so that all six share a single unit of measure. Unit of measure: mean item score on a 5-point Likert scale. The possible range for every subscale is a minimum of 1 to a maximum of 5, and a higher score indicates stronger belief on that construct, which is the better outcome. Each subscale difference is adjusted for the corresponding baseline subscale mean.
Measured: Baseline (Day 1), Day 1 post-intervention, and Week 4
Disaster Risk Perception Scale dimension scores
Between-arm differences in the five dimensions of the Disaster Risk Perception Scale (DRPS): exposure and impact, probability, uncontrollability, worry and fear, and vulnerability. Because the five dimensions contain different numbers of items, each dimension is reported on a common metric as the mean score of its constituent items, so that all five share a single unit of measure. Unit of measure: mean item score on a 5-point Likert scale. The possible range for every dimension is a minimum of 1 to a maximum of 5, and a higher score indicates greater perceived risk on that dimension, which is the direction of change the intervention is hypothesized to produce. Each dimension difference is adjusted for the corresponding baseline dimension mean.
Measured: Baseline (Day 1), Day 1 post-intervention, and Week 4
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Aug 2026
- Study start15 Oct 2026 (estimated)
- Primary completion20 Dec 2026 (estimated)
- Study completion20 Jan 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for DisastersStudies 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Two-arm, parallel-group, stratified cluster-randomized controlled trial. The unit of randomization is the intact school class (cluster); the unit of analysis is the individual student. Twelve classes are allocated 1:1, stratified by grade level (X, XI, XII). Within each class a random subsample of twelve students is drawn for outcome assessment before any class is randomized, and baseline data are collected from that subsample before allocation.
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 144 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Tanjungpura University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, I Made Moh. Yanuar Saifudin, Tanjungpura University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07781527
- Sponsor's protocol ID
- 5023/UN22.9/PT.01.04/2025
- Acronym
- DERAP
- Status last verified
- Aug 2026
- First submitted
- 16 Aug 2026
- Last updated
- 24 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: De-identified individual participant data underlying the published results, together with the data dictionary, will be made available by the principal investigator on reasonable request from qualified researchers whose proposed use has been approved by an independent review committee, subject to institutional and ethics-committee approval and a signed data-access agreement.
Study at a glance
From the registry record, last updated by the sponsor on 24 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effectiveness of an Audiovisual Disaster-Education Intervention on Disaster Risk Perception and Preparedness Belief Among Senior High-School Adolescents in West Kalimantan, Indonesia
- ClinicalTrials.gov ID
- NCT07781527
- Acronym / sponsor ID
- DERAP / 5023/UN22.9/PT.01.04/2025
- Conditions
- Disasters, Disaster Preparedness, Health Behavior, Risk Perception, Health Education, Adolescent Behavior
- Keywords
- disaster preparedness, disaster risk perception, Health Belief Model, audiovisual education, adolescents, school-based intervention, cluster randomized trial, Indonesia
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 144 participants (estimated)
- Lead sponsor
- Tanjungpura UniversityUniversity, hospital or other
- Study start
- 15 Oct 2026 (estimated)
- Primary completion
- 20 Dec 2026 (estimated)
- Study completion
- 20 Jan 2027 (estimated)
- First posted
- 24 Aug 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.
This cluster-randomized controlled trial tests whether a short, standardized disaster-education video improves two psychological precursors of disaster preparedness among senior high-school students in a hazard-prone district of West Kalimantan, Indonesia.
Twelve intact classes at one senior high school will be randomized 1:1, stratified by grade level, either to view a purpose-built audiovisual disaster-education module (approximately 20 minutes, shown twice in a single classroom session) or to view an attention-matched general adolescent-health video of similar length on an unrelated topic. Randomization is at the class level to reduce contamination between students, and the individual student is the unit of analysis. All students in a participating class view the video allocated to that class; a randomly drawn subsample of twelve students per class, 144 in total, completes the study questionnaires.
Two co-primary outcomes are measured in every participant. The first is disaster preparedness belief, measured by the General Disaster Preparedness Belief (GDPB) scale. The second is disaster risk perception, measured by the Disaster Risk Perception Scale (DRPS). Both are collected at baseline before allocation, immediately after the session, and again four weeks later.
The intervention and both instruments are grounded in the Health Belief Model, which predicts that raising perceived threat contributes to readiness to act. An exploratory mediation analysis will test whether change in risk perception explains part of any effect on preparedness belief.
After the four-week assessment, control classes are offered the full disaster-education intervention.
Detailed description
Background. West Kalimantan, including Kubu Raya Regency, is exposed to recurrent seasonal flooding and to land and forest fires with associated haze. Adolescents are rarely the explicit target of preparedness interventions despite being reachable at scale through schools, capable of transmitting preparedness knowledge within households, and themselves vulnerable during emergencies. Audiovisual media engage sight and hearing simultaneously, simplify complex content, and standardize delivery, making a short video a plausible low-cost vehicle for shifting the cognitive precursors of preparedness behavior.
Theoretical framework. The intervention is grounded in the Health Belief Model (HBM). Disaster risk perception corresponds to the upstream perceived-threat component of the HBM, comprising perceived susceptibility and perceived severity. Disaster preparedness belief captures the fuller, more downstream readiness-to-act constellation, combining threat appraisal with perceived benefits, perceived barriers, self-efficacy, and cues to action. Each content block of the video is mapped a priori to a specific HBM construct and to the outcome subscales it is intended to move, which is the content-validity rationale for using one shared intervention to address both co-primary outcomes.
Design. Two-arm, parallel-group, stratified cluster-randomized controlled trial with 1:1 allocation and a superiority framework. The cluster and unit of randomization is the intact class; the unit of analysis is the individual student. Stratification is by grade level (X, XI, XII), so that within each grade an equal number of classes is assigned to each arm. A computer-generated sequence is produced by the study statistician with the seed recorded. Class identifiers without class names are provided to an independent allocation holder who applies the sequence, giving third-party concealed allocation. Within each eligible class a random subsample of twelve students is drawn from the class roster before any class is randomized, and baseline data are collected from all consented students in that subsample before allocation, so that both participant selection and recruitment are complete before assignment is known. Drawing the subsample before allocation is essential, because selecting participants after clusters have been assigned is the principal source of identification and recruitment bias in cluster trials.
Masking. Participants and facilitators cannot be masked because the intervention is overt. Questionnaires are self-administered and identical across arms. The data manager who enters and cleans the data is masked to allocation, and the statistician conducts the primary analysis on an arm-coded dataset. Unmasking occurs only after the primary analysis is locked.
Sample size. Detecting a moderate standardized difference (Cohen d = 0.50) with two-sided alpha 0.05 and 80 percent power requires approximately 63 students per arm under individual randomization. Because the primary analysis adjusts for the baseline score, this requirement is multiplied by (1 minus r squared), where r is the assumed baseline-to-immediate-post correlation, taken as 0.60, giving approximately 40 students per arm. Twelve intact classes are randomized, six per arm, with twelve students randomly sampled and assessed within each class. The resulting design effect is 1 + (12 minus 1) x 0.05 = 1.55, giving approximately 62 evaluable students per arm. Allowing 15 percent attrition to the four-week follow-up gives an enrollment target of 72 students per arm and 144 in total. All students in participating classes view the assigned video; only the randomly drawn subsample completes the questionnaires. Under these assumptions the trial detects a standardized difference of approximately 0.50 at alpha 0.05, or approximately 0.56 under a Bonferroni-adjusted alpha of 0.025 for a joint co-primary claim. If the true intracluster correlation is 0.02, plausible for attitudinal outcomes, the detectable difference falls to approximately 0.45; if it is 0.10, it rises to approximately 0.59. The mediation analysis is powered only for exploratory purposes at this sample size.
Statistical analysis. For each co-primary outcome the primary analysis is a linear mixed-effects model with a random intercept for class and fixed effects for arm, time, and the arm-by-time interaction, adjusting for the baseline score, the stratification factor (grade), and pre-specified confounders (sex, age, prior personal disaster experience, prior exposure to disaster education). The treatment effect is the adjusted between-arm difference at the immediate post-intervention assessment, reported with a 95 percent confidence interval. Because the sample size claims credit for baseline adjustment, the observed baseline-to-post correlation will be reported alongside the primary result, as will the observed intracluster correlation for each outcome. Generalized estimating equations with an exchangeable working correlation are specified as an equivalent alternative. Baseline balance is described rather than significance-tested, following the Consolidated Standards of Reporting Trials (CONSORT) extension for cluster randomized trials. The primary analysis follows the intention-to-treat principle; a per-protocol analysis is secondary. Missing outcome data are handled by multiple imputation under a missing-at-random assumption with complete-case sensitivity analysis. Each co-primary outcome is tested at two-sided alpha 0.05 within its own analysis, and a Bonferroni-adjusted threshold of 0.025 is applied for any combined family-wise claim. The analysis plan is fixed before unmasking.
Fidelity and contamination. Every session is documented on a fidelity log recording that the correct video was played in full and twice, absence of interruptions or substituted content, adherence to the facilitator script, equipment and room conditions, attendance, and any deviation or contaminating event. Contamination within the single school is mitigated by randomizing at class level, separating data-collection days by arm, and scheduling control assessments so they are not preceded by discussion with intervention classes. Residual contamination is expected to bias effects toward the null.
Post-trial provision. After the four-week assessment, control classes are offered the full audiovisual disaster-education intervention.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
- Model description
- Two-arm, parallel-group, stratified cluster-randomized controlled trial. The unit of randomization is the intact school class (cluster); the unit of analysis is the individual student. Twelve classes are allocated 1:1, stratified by grade level (X, XI, XII). Within each class a random subsample of twelve students is drawn for outcome assessment before any class is randomized, and baseline data are collected from that subsample before allocation.
| Arm | Type | Receives |
|---|---|---|
| Audiovisual disaster-education module | Experimental | Behavioral: Audiovisual disaster-education moduleClasses allocated to this arm receive, in a single standardized classroom session, a purpose-built audiovisual disaster-education module of approximately 20 minutes, played twice consecutively, optionally followed by a fully scripted five-minute facilitator debrief in which each student names one personal preparedness action. Content blocks cover the definition of disaster, how disasters occur, impacts and risks, benefits of preparedness, personal preparation steps, barriers and misconceptions, social and environmental roles, self-efficacy, environmental knowledge, and a closing call to action, each mapped to a Health Belief Model construct. Delivery is standardized (identical file, equipment, and room set-up) by a trained facilitator following a fixed script and completing a fidelity checklist. |
| Attention-matched general-health video | Active comparator | Behavioral: Attention-matched general-health videoClasses allocated to this arm receive, in an equivalent session of similar length and under identical conditions, a general adolescent-health video unrelated to disaster preparedness (for example, on personal hygiene or balanced nutrition). This attention-matched comparator controls for contact time, facilitator attention, and the novelty of receiving a video session, isolating the specific effect of the disaster content. After the four-week follow-up assessment, classes in this arm are offered the full audiovisual disaster-education intervention. |
Who may qualify
- Ages
- 15 to 19 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (7 listed)
- Intact class of grade X, XI, or XII within the participating school
- 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
Key exclusion criteria (6 listed)
- Class unavailable for the full schedule of sessions during the study window (for example, examination or fieldwork commitments)
- 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
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 |
|---|---|---|
| Audiovisual disaster-education moduleAlso: disaster-education video, DERAP (Disaster Education for Risk-perception And Preparedness) videoA purpose-built educational video on disaster preparedness, approximately 20 minutes in duration, developed through a structured instructional-design cycle (needs analysis, learning objectives, storyboard, production, expert content validation withitem-level content validity index [I-CVI] of at least 0.78 and scale-level content validity index, average method [S-CVI/Ave], of at least 0.90, comprehension pilot, and lock). The defined dose is one viewing repeated twice in the same session, identical for every intervention cluster. An optional fully scripted five-minute debrief may follow. No deviation from this dose is permitted without a documented protocol amendment. | Behavioural | Audiovisual disaster-education module |
| Attention-matched general-health videoAlso: Attention control videoA general adolescent-health video on a topic unrelated to disaster preparedness (for example, personal hygiene or balanced nutrition), matched to the experimental module for duration, delivery format, room conditions, and facilitator contact time. | Behavioural | Attention-matched general-health video |
Primary outcome
Change in disaster risk perception, measured by the Disaster Risk Perception Scale total score
Time frame: Baseline (Day 1, pre-intervention) and Day 1, within 30 minutes post-intervention
Disaster risk perception measured by the Disaster Risk Perception Scale (DRPS), a 25-item instrument covering five dimensions: exposure and impact, probability, uncontrollability, worry and fear, and vulnerability. Each item is scored on a 5-point Likert scale from 1 (strongly disagree) to 5 (strongly agree). The total score is the sum of all 25 items and ranges from a minimum of 25 to a maximum of 125. A higher total score indicates greater perceived disaster risk. Higher scores are not inherently better or worse for health; greater perceived risk is the direction of change the intervention is hypothesized to produce, because perceived threat is the upstream component of the Health Belief Model. The estimand is the between-arm difference in DRPS total score immediately post-intervention, adjusted for the baseline score, grade, and pre-specified confounders, estimated in a linear mixed-effects model with a random intercept for class.
Change in disaster preparedness belief, measured by the General Disaster Preparedness Belief scale total score
Time frame: Baseline (Day 1, pre-intervention) and Day 1, within 30 minutes post-intervention
Disaster preparedness belief measured by the General Disaster Preparedness Belief (GDPB) scale, a 38-item instrument based on the Health Belief Model. Each item is scored on a 5-point Likert scale from 1 (strongly disagree) to 5 (strongly agree), with negatively worded items reverse-scored before summation. The total score is the sum of all 38 items and ranges from a minimum of 38 to a maximum of 190. A higher total score indicates stronger disaster preparedness belief, which is the better outcome. The estimand is the between-arm difference in GDPB total score immediately post-intervention, adjusted for the baseline score, grade, and pre-specified confounders, estimated in a linear mixed-effects model with a random intercept for class.
4 secondary outcomes
Retention of effect on disaster preparedness belief at four weeks, measured by the General Disaster Preparedness Belief scale total score
Time frame: Baseline (Day 1) and Week 4
Retention of effect on disaster risk perception at four weeks, measured by the Disaster Risk Perception Scale total score
Time frame: Baseline (Day 1) and Week 4
General Disaster Preparedness Belief scale subscale scores
Time frame: Baseline (Day 1), Day 1 post-intervention, and Week 4
Disaster Risk Perception Scale dimension scores
Time frame: Baseline (Day 1), Day 1 post-intervention, and Week 4
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 24 Aug 2026.
- Individual participant dataSharing planned: Yes. De-identified individual participant data underlying the published results, together with the data dictionary, will be made available by the principal investigator on reasonable request from qualified researchers whose proposed use has been approved by an independent review committee, subject to institutional and ethics-committee approval and a signed data-access agreement.
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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.
I Made Moh. Yanuar Saifudin, S.Kep., Ns., M.Kep. contact
Questions about this trial
What is this clinical trial studying?
A study testing Audiovisual disaster-education module and Attention-matched general-health video in people with Disasters and Disaster Preparedness, run by Tanjungpura University.
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 7 inclusion and 6 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: opening soon, as of the sponsor's last update on 24 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
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?
Contact I Made Moh. Yanuar Saifudin, S.Kep., Ns., M.Kep. (+6281225438514, imademohyanuar.s@ners.untan.ac.id), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in disaster risk perception, measured by the Disaster Risk Perception Scale total score (time frame: Baseline (Day 1, pre-intervention) and Day 1, within 30 minutes post-intervention). The study lists 2 primary outcomes in all. 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 24 Aug 2026.