The Impact of Medical TV Drama in Improving Literacy on Asthma
NCT ID: NCT07262918
Last Updated: 2025-12-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
48 participants
INTERVENTIONAL
2025-12-25
2026-04-25
Brief Summary
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Detailed Description
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METHODS Study Design This study will be an online, open-label, parallel-group, two-arm RCT, a rigorous design widely used to evaluate the effectiveness of health interventions. The trial will aim to determine the impact of a medical TV drama episode on asthma-related health literacy among young adults. The design will be informed by evidence suggesting that entertainment media can enhance health knowledge and influence behavior change. Participants will be randomly assigned to either an intervention group (who will view the episode) or a control group (with no exposure), and their knowledge scores will be compared before and after the intervention. The study will follow the CONSORT (Consolidated Standards of Reporting Trials) 2010 guidelines for the reporting of RCTs.
Study Setting and Participants. The trial will be conducted entirely online, a delivery model increasingly adopted for its cost-efficiency, accessibility, and potential to reach a geographically diverse population. Participants will be recruited using social media platforms such as Facebook, Instagram, WhatsApp, and X (formerly Twitter), which have previously been shown to be effective for digital recruitment in health research.
Only those who provide consent will be enrolled in the study, in accordance with ethical guidelines for digital health research.
Sample Size Determination The sample size will be calculated using G\*Power version 3.1, a well-established tool for statistical power analysis. Assuming a two-tailed independent samples t-test, an alpha level of 0.05, a power of 0.80, and a large effect size (Cohen's d = 0.83), the minimum required sample size will be 48 participants, with 24 participants per group. This sample size will provide sufficient power to detect large differences in asthma-related knowledge outcomes.
Randomization and Allocation Following informed consent, participants will be randomly assigned in a 1:1 ratio to either the intervention or control group. Randomization will be executed manually using a balloting technique, ensuring equal allocation and minimizing allocation bias. Due to the visible nature of the media intervention, participant blinding will not be possible, and the study will therefore adopt an open-label design.
Intervention Participants in the intervention arm will be asked to watch House M.D., Season 1, Episode 1, which includes dramatized depictions of asthma-related clinical scenarios. Prior research has demonstrated that medical TV dramas can enhance viewers' health literacy and influence decision-making, particularly in younger audiences. After viewing the episode, participants will complete a structured post-test questionnaire.
Participants in the control group will complete the same questionnaire at the same time intervals but will not view the media intervention. No additional educational content will be provided to either group during the study period.
Study Instruments The study instruments that will be used in this RCT are a pre-test and a post-test questionnaire. Both questionnaires will obtain, inter alia, data on the sociodemographic characteristics of the participants and their knowledge of asthma.
To ensure content validity, the initial draft of the questionnaire will be reviewed by two clinical experts in respiratory medicine. A pilot test involving five individuals (meeting the inclusion criteria but excluded from the trial) will be conducted to evaluate clarity, comprehension, and administration time. Feedback from the pilot will inform minor revisions to item structure and wording.
Participants in the intervention group will complete the questionnaire as a pre-test before viewing the episode and a post-test immediately afterward. Control group participants will complete the same questionnaire at matched time points without viewing the episode. Each correct answer will score one point, yielding a maximum score of 10. This outcome measure is focused exclusively on cognitive knowledge acquisition, and no secondary outcomes such as behavioral intent or media perception will be assessed.
Data will be collected using encrypted digital forms via Google FormsĀ®. All responses will be time-stamped and automatically stored on password-protected institutional servers accessible only to the research team. Responses with more than 20% missing data will be excluded from analysis to ensure quality. Additional quality control procedures will include screening for contradictory answers, unusually fast completion times (e.g., under one minute), and potential duplicate submissions identified via IP and timestamp monitoring.
Statistical Analysis Descriptive statistics, including means, standard deviations, and frequencies, will be used to summarize participant demographics and outcome data. For inferential analysis, paired t-tests will be applied to assess within-group changes in knowledge scores (pre- vs. post-test), while independent samples t-tests will compare changes between the intervention and control groups. The Shapiro-Wilk test will be used to evaluate the normality of score distributions. When normality assumptions are violated, appropriate non-parametric tests such as the Wilcoxon signed-rank test and Mann-Whitney U test will be used. A p-value \< 0.05 will be considered statistically significant.
Ethical Considerations Ethical approval has been obtained from the Institutional Review Board of Caleb University, Nigeria (CUL 25/0877). All participants will provide electronic informed consent before enrolment. They will be informed of their right to withdraw from the study at any time without penalty. All procedures will comply with international ethical standards for digital research involving human subjects.
Trial Timeline Participant recruitment and pre-test will be done in Weeks 2 and 3. The intervention will be administered in Week 4, and post-test will be done in Weeks 8 to 9. Data cleaning and analysis were conducted in Weeks 10 and 11, and the results will be compiled and disseminated in Weeks 12 to 16.
Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
PREVENTION
NONE
Study Groups
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CONTROL ARM (NO MEDIAL INTERVENTION)
NO INTERVENTION
No interventions assigned to this group
INTERVENTION ARM (MEDIAL INTERVENTION)
MEDIAL INTERVENTION
TELEVISION DRAMA
MEDICAL TV DRAMA
Interventions
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TELEVISION DRAMA
MEDICAL TV DRAMA
Eligibility Criteria
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Inclusion Criteria
* Individuals who are proficient in English.
* Individuals who have access to a stable internet connection, a screen-enabled device, and Netflix movie platform.
Exclusion Criteria
* Individuals with a clinical history of asthma.
* Individuals who do not have access toa stable internet connection, a screen-enables device, or Netflix movie platform.
* Individuals who are aged below 18 years or above 35 years.
* Individuals who are concurrently participating in another asthma-related study.
18 Years
35 Years
ALL
Yes
Sponsors
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Cephas Health Research Initiative Inc, Ibadan, Nigeria
NETWORK
Responsible Party
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Emeka Okeke
Director
Central Contacts
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References
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1. WHO Fact Sheet on asthma. Available online from https://www.who.int/. Accessed May 18, 2025. 2. Moris MJ. Asthma: practice, essentials, background, anatomy. Available online from https://emedicine.medscape.com/article/296301-overview#a1. Accessed May 18, 2025. 3. GBD 2021 Asthma and Allergic Diseases Collaborators. Global, regional, and national burden of asthma and atopic dermatitis, 1990-2021, and projections to 2050: a systematic analysis of the Global Burden of Disease Study 2021. Lancet Respir Med. 2025;13(5):425-446. doi:10.1016/S2213-2600(25)00003-7 4. Yuan L, Tao J, Wang J, et al. Global, regional, national burden of asthma from 1990 to 2021, with projections of incidence to 2050: a systematic analysis of the global burden of disease study 2021. eClinicalMedicine, Volume 80, 103051 5. Nunes C, Pereira AM & Morais-Almeida, M. Asthma costs and social impact. asthma res and pract . 2017;3(1). https://doi.org/10.1186/s40733-016-0029-3 6. Chan YY, Teh CH, Lim KK et al. Lifestyle, chronic diseases and self-rated health among Malaysian adults: results from the 2011 National Health and Morbidity Survey (NHMS). BMC Public Health. 2015;15(1). 7. Aneeshkumar S, Singh RB. Economic burden of asthma among patients visiting a private hospital in South India. Lung India. 2018 Jul-Aug;35(4):312-315. doi: 10.4103/lungindia.lungindia_474_17. 8. Ndarukwa P, Chimbari MJ & Sibanda EN. Development of a framework for increasing asthma awareness in Chitungwiza, Zimbabwe. asthma res and pract 5, 4 (2019). https://doi.org/10.1186/s40733-019-0052-2 9. Poureslami IM, Rootman I, Balka E, Devarakonda R, Hatch J, Fitzgerald JM. A systematic review of asthma and health literacy: a cultural-ethnic perspective in Canada. MedGenMed. 2007 Aug 21;9(3):40. 10. Basima A Almomani, Shoroq M Altawalbeh, Munther S Alnajjar, Suleiman M Momany, Assessment of medication knowledge among patients with asthma, Journal of Pharmaceutical Health Services Research, Volume 11, Issue 4, November 2020, Pages 349-354, https://doi.org/10.1111/jphs.12383 11. Basheti IA, Obeidat NM, Reddel HK. Inhaler technique education and asthma control among patients hospitalized for asthma in Jordan. Saudi Pharm J. 2018;26(8):1127-1136. doi:10.1016/j.jsps.2018.06.002 12. Dhruve H. Management of asthma: Adherence, inhaler technique and self-management. Practice Nursing 2018; 29: 4. 13. WHO 14. Orozco-Olvera V, Shen F, Cluver L. The effectiveness of using entertainment education narratives to promote safer sexual behaviors of youth: A meta-analysis, 1985-2017. PLoS One. 2019 Feb 12;14(2):e0209969. doi: 10.1371/journal.pone.0209969. 15. Francis A, Abraham E, Verma G, et al. (September 21, 2024) Assessment of Knowledge and Attitude of Asthmatic Patients and Their Caregivers Regarding the Disease Using an Asthma Knowledge Questionnaire in a Tertiary Care Hospital in Chennai. Cureus 16(9): e69832. doi:10.7759/cureus.69832
Other Identifiers
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CUL25/0877
Identifier Type: -
Identifier Source: org_study_id
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