AzTrials
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DisasterNCT07296367

Physiotherapy and Disaster

An observational study of Disaster and Physiotherapist Students, run by Uşak University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this observational study is to examine the relationships between disaster response self-efficacy, psychological preparedness for disaster threats, and interdisciplinary readiness levels among undergraduate Physiotherapy and Rehabilitation students. Read more about this study

Who is it for?
Ages 18 to 49 yearsHealthy volunteers can take part
Conditions the study is for
Disaster, Physiotherapist Students
How many people
390 participants
Where
1 siteTurkey (Türkiye)
Study dates
20 Dec 2025to 10 Feb 2026
Phase
Observational
Are there results?
None posted in the registry

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 to 49 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: The study population consists of undergraduate students studying in Physiotherapy and Rehabilitation departments in Türkiye. Participants will include 1st, 2nd, 3rd, and 4th-year students between the ages of 18 and 49 who voluntarily agree to participate and complete the online informed consent and questionnaire form. Data collection will be carried out through online surveys distributed to students enrolled at Pamukkale University, İnönü University, and Alanya Alaaddin Keykubat University.

Who may be able to join

  • Being an undergraduate student (1st-4th year) in a Physiotherapy and Rehabilitation program at a university in Türkiye
  • Being 18 to 49 years of age at the time of participation.
  • Reading and providing electronic informed consent on the online form.
  • Completing the online questionnaire in full.

Who cannot join

  • Not being enrolled as an undergraduate student in a Physiotherapy and Rehabilitation program, or not being in 1st-4th year.
  • Not providing electronic informed consent.
  • Completing the survey partially or with clear errors (e.g., missing or invalid responses).
  • Duplicate entries detected as the same participant filling in the questionnaire more than once.
  • Leaving more than 50% of the items unanswered or providing highly inconsistent response patterns that compromise data reliability.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Pamukkale University

    Denizli, Denzili, 20160

Other trials in Turkey (Türkiye)

About this study

Official title: Examining the Relationship Between Disaster Response Self-efficacy, Psychological Preparedness, and Interdisciplinary Readiness in Physiotherapy Students

The purpose of this observational study is to examine the relationships between disaster response self-efficacy, psychological preparedness for disaster threats, and interdisciplinary readiness levels among undergraduate Physiotherapy and Rehabilitation students. The study will be conducted among students studying in the Physiotherapy and Rehabilitation departments of Pamukkale University, İnönü University, and Alanya Alaaddin Keykubat University in Turkey.

Participants will complete online surveys regarding disaster preparedness while continuing their routine education as part of their active learning. No clinical practice, medical intervention, or experimental procedures will be conducted in the study.

Read more

The primary research question of this study is:

Is there a significant relationship between the disaster response self-efficacy, psychological preparedness, and interdisciplinary readiness levels of physiotherapy students? Data will be collected voluntarily via Google Form; students can withdraw from the study at any time. Personal information will not be collected, and all data will be analyzed solely for scientific purposes, in accordance with confidentiality principles. While no medical or physical benefits are expected for participants, the findings are expected to contribute to the development of physiotherapy training curricula for disaster preparedness and crisis management.

The study will commence in December 2025 following ethics committee approval, and the entire process, including data collection, is planned to take approximately six months.

Read the detailed description

This observational study aims to examine the relationships among physiotherapy students' disaster response self-efficacy, psychological preparedness for disaster threats, and interdisciplinary readiness levels. Data will be collected and analyzed from volunteer participants via an online survey. No experimental interventions, treatments, or clinical procedures will be implemented in the study. Participant safety and data confidentiality will be protected in accordance with ethical principles. The findings are expected to contribute to the development of disaster preparedness regulations in physiotherapy education programs.

Keywords
Disaster response self-efficacy, Interdisciplinary readiness, Physiotherapy students, Disaster management, Psychological preparedness

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07296367
Study groupRoleWhat they receive
physiotherapy studentsphysiotherapy students studying at different universities

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Disaster self-efficacy level

    • Measurement tool: Disaster Response Self-Efficacy Scale (DRESES)
    • Purpose: To assess the perception of competence to respond effectively during a disaster.

    Measured: Single assessment at baseline (Day 1).

Secondary outcomes (2)
  1. Interdisciplinary Readiness Level

    • Measurement tool: Readiness for Interprofessional Learning Scale (RIPLS)
    • Purpose: To determine readiness for collaboration in post-disaster healthcare services.

    Measured: Single assessment at baseline (Day 1).

  2. Psychological Preparedness Level for Disaster Threats

    • Measurement tool: Psychological Preparedness for Disaster Threats Scale (PPDTS)
    • Variable type: Continuous (Likert total score)
    • Purpose: To determine students' psychological resilience and preparedness levels for disaster situations.

    Measured: Single assessment at baseline (Day 1).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Dec 2025
  2. Study start20 Dec 2025
  3. Primary completion10 Feb 2026
  4. Study completion10 Feb 2026

Resources

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
Cross-sectional
Enrolment
390 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07296367
Sponsor's protocol ID
E-60116787-020-789573
Status last verified
Dec 2025
First submitted
8 Dec 2025
Last updated
7 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Because data is collected entirely on a voluntary basis, protecting participant privacy is a priority. Therefore, there are no plans to share Individual Participant Data (IPD) with third parties.

Questions about this trial

What is this clinical trial studying?

An observational study of Disaster and Physiotherapist Students, run by Uşak University at 1 site in Turkey (Türkiye).

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 4 inclusion and 5 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: finished, as of the sponsor's last update on 7 May 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 Turkey (Türkiye). 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Disaster self-efficacy level (time frame: Single assessment at baseline (Day 1).). 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 7 May 2026.

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