An interventional study of Health Belief Model -Based Disaster Education in Disaster Preparedness, Health Education and Child With Special Health Care Needs, sponsored by Ataturk University. Not yet recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-09.
Sponsored by Ataturk University · Not applicable, Interventional, and Prevention
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Among 85 studies in Health Education with a site in Turkey — 10 open to participants now, 16 under way, none of them phase 3. Health Education · Turkey.
Among the 85 studies in Health Education with a site in Turkey, this one is the 48th largest by planned enrollment of the 79 interventional ones that give a count, is one of 19 that started in 2026, is one of 79 with no phase, reaches primary completion later than 9 of the 15 other live ones, and was the 82nd registered.
483 studies on the registry are indexed under Health Education; 112 are open to participants now.
Browse Health Education studies →10 of the 85 studies in Health Education with a site in Turkey are open now. Recruiting first, the newest first:
Esra ÖZER · Sites in Turkey
Women only · Healthy volunteers
Gaziantep Islam Science and Technology University · Sites in Turkey
Ages 19–65 · Men only · Healthy volunteers
Sakarya University · Sites in Turkey
Ages 14–17 · Healthy volunteers
Osmaniye Korkut Ata University · Sites in Turkey
Women only · Healthy volunteers
Lokman Hekim University · Sites in Turkey
Ages 18+
A study can be open while its sites in Turkey have not opened yet or have stopped. Only those recruiting at a site in Turkey →
Of the 46 Health Education studies recruiting now, 29 (63%) set no upper age limit and 14 (30%) stop at 75 or younger; 11 take children under 18; 18 take healthy volunteers.
This study: 18 Years to 65 Years · all sexes · healthy volunteers too.
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85 studies; the count open now beside each. This study's row is marked.
First in 2017; this study’s year is marked. 19 started in 2026.
This study's planned enrollment of 80 is below the median of 132 across 452 interventional studies indexed under Health Education.
Median enrollment 100 across the 79 interventional studies, 162 across the 6 observational. Of the 67 that completed or were terminated, 0 (0%) have results posted.
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None of the 85 has an industry lead sponsor. The 10 most frequent:
Ataturk University is the lead sponsor of 460 studies on the registry; 126 are open to participants now.
Ataturk University has 2 studies filed under Health Education — fewer than ten, so there is no comparison to draw.
4 of the studies in Health Education with a site in Turkey that are under way reach primary completion within a year, 0 of them phase 3. Phase 3 first, then by date:
| Study | Primary completion |
|---|---|
| NCT07922057Sakarya UniversityMobile Game-Based Versus Classic First Aid Education in Adolescents: Randomized Controlled Trial | 2026-11-17 |
| NCT07812532Lokman Hekim UniversityEffect of Gamified Sun Protection Education Provided to Chemotherapy Patients | 2026-11-30 |
| NCT07295639Gaziantep Islam Science and Technology UniversityMobile Prenatal Education for Expectant Fathers and Its Effects on Bonding, Stress, Breastfeeding and Marital Satisfaction | 2027-03 |
| NCT07774494Osmaniye Korkut Ata UniversityEffect of AI-Assisted Discharge Education on Parents of Children With Bronchitis/Bronchiolitis | 2027-06-15 |
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Among the 85 studies in Health Education with a site in Turkey, from their registry updates:
This tab as a report to print or save as PDF → With an account.
This study aims to evaluate the effect of a Health Belief Model (HBM)-based disaster education program on general disaster preparedness beliefs and disaster preparedness levels among parents of children with special needs. Children with special healthcare and developmental needs are particularly vulnerable during disasters, and parental readiness plays a critical role in mitigating risks. The study is designed as a quasi-experimental (or randomized controlled) interventional trial with an intervention and a control group to determine whether structured, model-based training improves preparedness behaviors and disaster beliefs among parents.
This study is conducted between September 2026 and October 2026 at the Ozel Mavi Special Education and Rehabilitation Center in Diyarbakir, Turkey. The center consists of two separate service buildings within the same campus, providing individualized and group special education services for children diagnosed with autism spectrum disorder, intellectual disability, specific learning disorders, attention deficit hyperactivity disorder (ADHD), and speech/language impairments.
Parents are recruited during their children's active educational sessions. Participants are allocated into intervention and control groups. The intervention group receives a structured, 5-week Health Belief Model-based disaster preparedness training program, while the control group receives routine follow-up (or standard institutional guidance).
Outcome assessments include baseline (pre-test) measurements and post-intervention (post-test) evaluations conducted after the completion of the 5-week educational program. Primary outcomes measure participants' general disaster preparedness beliefs and objective disaster preparedness levels.
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.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Parents receive a structured Health Belief Model (HBM)-based disaster education program along with routine follow-up.
Behavioral: Health Belief Model -Based Disaster Education
Parents receive standard care/routine follow-up during the study period. To ensure ethical standards, the Health Belief Model-based disaster education program is delivered to this group after all post-test data collection is completed.
A 5-week structured disaster preparedness education program based on the Health Belief Model, covering disaster risks, preparedness behaviors, individual emergency planning, and safety measures tailored for parents of children with special needs.
Change in General Disaster Preparedness Beliefs Scale Score
Assessed using the General Disaster Preparedness Beliefs Scale based on the Health Belief Model. Evaluates perceived susceptibility, perceived severity, perceived benefits, perceived barriers, and self-efficacy regarding disaster preparedness. Higher scores indicate higher preparedness beliefs.
Time frame: Baseline (pre-test) and 5 weeks after the intervention (post-test)
Change in Disaster Preparedness Level Score
Assessed using the Disaster Preparedness Scale to evaluate physical and cognitive preparedness behaviors, emergency planning, and safety precautions among parents. Higher scores indicate higher readiness levels.
Time frame: aseline (pre-test) and 5 weeks after the intervention (post-test)
Plan to share: No
No publications or documents are linked to this record.
Start is estimated for Sep 2026; primary completion for Oct 2026, 1 month later.
Of 292 non-industry interventional studies with no phase under Health Education, half reached primary completion within 11 months of starting (the median), counting those still running; a quarter within 3 and three quarters within 24. This study's planned 1 month is below that.
Counting every sponsor, half of 293 studies reached it within 11 months; a quarter within 3 and three quarters within 24.
How these figures are worked out, and which studies are left out of them.
This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.
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