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Clinical Trials in India / NCT06711848
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Testing and Comparing the Impacts of Mhealth-Based and Web-Based Education on Oral Cancer

NCT06711848 · tracked via the Priya Life Science India tracker
Sponsor
University of Rwanda
Phase
Not applicable
Started
2025-01-05
Last updated
2024-12-02

Condition(s) studied

Oral CancerHealth Education, CommunityDigital InterventionMHealth ApplicationMHealth Intervention

Investigational drug(s) / intervention(s)

A web-based educational intervention on oral cancerA mobile health app-based educational intervention on oral cancer

A web-based educational intervention on oral cancer: This intervention will involve administering education, via a website, on the meaning, risks, clinical features, prevention, treatment, and supports on oral cancer.

A mobile health app-based educational intervention on oral cancer: This intervention will involve administering education, via a mhealth application prototype, on the meaning, risks, clinical features, prevention, treatment, and supports on oral cancer.

Study summary

Introduction: Oral cancer is a malignant neoplastic disease affecting the lip, oral cavity (mouth) and/or the oropharynx. Despite the intense and diverse public health interventions on oral cancer prevention, the global prevalence rates of oral cancer and its major risk factors are still very high. Hence, oral cancer is an issue of serious global health importance.

Aim: To test and compare the effectiveness, usability, uptake, and acceptability of an educational website and a mobile health application prototype on oral cancer in improving oral cancer knowledge among university students.

Methods: This study will adopt a randomised control trial design, and it will be conducted among 75 first-year bachelor's degree students from five universities across two continents: University of Rwanda (Rwanda, Africa), Usmanu Danfodiyo University (Nigeria, Africa), University of Peradeniya (Sri Lanka, Asia), University of Ibadan (Nigeria), and Saveetha University (India, Aisa). The study participants will be in three groups (Group 1, Group 2, and Group 3). The participants in Group 1 will be the control group (n = 25 participants; 5 participants from each university); that is the group that will not receive an educational intervention. However, those in Group 2 (n = 25 participants; 5 participants from each university) will receive a web-based educational intervention on oral cancer while those in Group 3 (n = 25 participants; 5 participants from each university) will receive an app-based educational intervention on oral cancer. Pretest survey and posttest survey will be done for all participants. The data collected will be statistically analysed using the Statistical Package for Social Sciences (SPSS) version 28 software. Descriptive statistics will be done for all variables while inferential statistics (analysis of variance) will be done to test for associations between variables of interest.

Conclusion: The findings of this study will determine the effectiveness, usability, uptake, and acceptability of the tested digital intervention tools.

Eligibility

Sex
ALL
Min age
18 Years
Max age
39 Years
Healthy volunteers
Accepted
Inclusion Criteria: * being a first-year bachelor degree student of either University of Rwanda (Rwanda), University of Peradeniya (Sri Lanka), Usmanu Danfodiyo University (Nigeria), University of Ibadan (Nigeria), or Saveetha University (India) * being within the age range of 18 to 39 years * having a personal smartphone * willingness to participate in the study Exclusion Criteria: * being a member of staff or a visitor or a non-first year bachelor degree student of University of Rwanda (Rwanda), University of Peradeniya (Sri Lanka), Usmanu Danfodiyo University (Nigeria), University of Ibadan (Nigeria), or Saveetha University (India) * being a student of a tertiary institution not selected for the study * being below the age of 18 years or above the age of 39 years. * not having a personal smartphone * not willing to participate in the study

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
Saveetha University Tamil Nadu India
University of Ibadan Ibadan Oyo State
Usmanu Danfodiyo University Sokoto Sokoto State
University of Rwanda Kigali Kigali
University of Peradeniya Peradeniya Sri Lanka

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06711848 on ClinicalTrials.gov ↗ ← All trials in India