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NCT Number: NCT07048301

Omaha System-Based Health Application on Improving Knowledge, Attitude, and Behaviors Regarding Infectious Disease Prevention in the Community

Background: Infectious diseases remain significant public health concerns due to several factors such as climate and environmental changes and natural disasters. Mobile health applications (mHealth apps) can be an appropriate way for fostering community participation, disseminating knowledge, and promoting behavior change toward infectious disease prevention. This study aims to describe a protocol for a pilot randomized controlled study to evaluate the impact of the Omaha System-Based mHealth app (BUHOS) on improving knowledge, attitude, and behaviors (KAB) regarding infectious disease prevention in an earthquake-affected region of Türkiye.

Methods: This study is a two-armed, parallel-group, randomized controlled trial design. A total of 112 eligible participants will be recruited from two separate container cities of an earthquake-affected region. These participants will be randomly allocated to either an intervention group or a control group. BUHOS will be designed based on the Omaha System, a widely recognized standardized taxonomy for the assessment, planning, and evaluation of healthcare services. BUHOS will be a two-week nursing intervention that includes monitoring KAB, employing Education, Guidance and Counseling (education videos), and Surveillance (reminder messages), and assessing the outcomes. Outcome variables will include the Problem Rating Scale for Outcomes, Community Communicable Diseases Knowledge Survey, Communicable Diseases Risk Awareness and Protection Scale and System Usability Scale. Outcome variables will be assessed on the 15th and 30th day after intervention.

Hypotheses:

H1: Among the Omaha System Problems, the Communicable/ Infectious Condition Problem Knowledge score will be higher on the 15th and 30th days compared to the control group.

H2: Infectious diseases risk awareness and prevention score will be higher on the 15th and 30th days compared to the control group.

H3: Communicable/ Infectious Condition Status Behaviour Parameter score will be higher on the 15th and 30th days compared to the control group H4: The knowledge and behaviour of the communicable/ infectious status and the awareness and prevention of the risk of infectious diseases of the experimental group will be higher than before the intervention on the 15th and 30th days.

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Key information

Age range

18 year–64 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • being aged between 18 and 64 years,
  • living in two container cities,
  • having a knowledge score of 'very low (1)' and 'low (2)' on the Omaha System Problem Rating Scale for Outcome for Communicable/ Infectious Problem Knowledge Parameter,
  • being literate,
  • owning a smartphone.

Exclusion criteria

  • having impaired vision or hearing,
  • having a mental illness,
  • not owning a smartphone,
  • being pregnant or postpartum,
  • being participants in another scientific study,
  • refusing to participate.

Treatment and study plan

BUHOS app

Other

In this study, the BUHOS app initiative will be implemented among participants in the intervention group. BUHOS will be a two-weeks nursing intervention that includes monitoring KAB, employing Education, Guidance and Counseling (education videos), and Surveillance (reminder messages), and assessing the outcomes.

Control Group

Other

No intervention will be made to the patients in the control group, and the training videos prepared after the study is completed will be shared.

Primary outcomes

  1. Omaha System- Problem Rating Scale for Outcomes Knowledge parameter

    Time frame: 15th and 30th day after intervention

  2. Omaha System- Problem Rating Scale for Outcomes Behavior parameter

    Time frame: 15th and 30th day after intervention

  3. Communicable Diseases Risk Awareness and Protection Scale (CDRAPS)

    Time frame: 15th and 30th day after intervention

  4. Community Communicable Diseases Knowledge Survey

    Time frame: 15th and 30th day after intervention

Secondary outcomes

  1. System Usability Scale (SUS)

    Time frame: 30th day after intervention

Study contacts

Contact information is provided by the study sponsor or research team.

Gizemnur Torun, PhD.

CONTACT

[email protected]

+902623034722

Merve Altıner Yaş, Assistant Professor

CONTACT

Sponsors and collaborators

Lead sponsor

Kocaeli University

Other

Collaborators

  • Atlas University
  • Hatay Devlet Hastanesi
  • Health Institutes of Turkey
  • Istanbul Medeniyet University
  • Istanbul University - Cerrahpasa

Registry information

Official study title

Developing an Omaha System-Based Health Application on Improving Knowledge, Attitude, and Behaviors Regarding Infectious Disease Prevention in the Community

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Jul 2, 2025
Registry last updated
Jul 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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