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The Effect of Structured Health Information-Seeking Training on Cyberchondria and E-Health Literacy in Menopausal Women: A Randomized Controlled Trial

17 september 2026 bijgewerkt door: Merve Tuncer, Istanbul University

This randomized controlled study will examine whether two different forms of structured health information-seeking education can help women in perimenopause or postmenopause use online health information more effectively. It will assess whether video-based education and Pecha Kucha-based education reduce cyberchondria, which refers to repeated online health searches that may increase health-related worry, and improve e-health literacy and knowledge about menopause.

The study will include 60 women aged 40 to 65 years. Participants will be randomly assigned in a 1:1:1 ratio to a video-based education group, a Pecha Kucha-based education group, or a control group, with 20 participants in each group. The education will cover how to identify reliable online health sources, evaluate health information, recognize misleading content, use effective search methods, and avoid online searching behaviors that may increase anxiety. The control group will not receive structured education during the study period. Outcomes will be assessed before the intervention, immediately after the intervention, and one month later. The findings will help determine which educational method is more effective in supporting safe and informed online health information-seeking among women during the menopausal transition.

Studie Overzicht

Gedetailleerde beschrijving

The increasing use of the internet as a source of health information may help women access information about menopause, but it may also expose them to inaccurate, misleading, or anxiety-provoking content. Repeated online searching for symptoms and diseases may increase health-related worry and contribute to cyberchondria. Therefore, the ability to find, understand, evaluate, and appropriately use online health information is particularly important during the menopausal transition.

This study is designed as a three-arm, parallel-group randomized controlled trial to compare the effects of video-based and Pecha Kucha-based structured health information-seeking education among women in perimenopause or postmenopause. A total of 60 women will be randomly assigned in a 1:1:1 ratio to the video-based education group, the Pecha Kucha-based education group, or the control group. Each group will include 20 participants.

Participants in the video-based education group will receive structured health information-seeking education through a video. Participants in the Pecha Kucha-based education group will receive structured education through a concise, visually focused Pecha Kucha presentation. Both educational approaches will address the benefits and risks of seeking health information online, methods for identifying reliable sources, evaluation of authorship and scientific evidence, recognition of advertising and misleading content, effective search strategies, verification of information across multiple sources, and strategies for limiting repetitive online searches that may increase anxiety. The control group will not receive structured health information-seeking education during the study period.

Data will be collected from all three groups at three time points: before the intervention, immediately after the intervention, and one month after the intervention. The study will examine changes in cyberchondria severity, e-health literacy, and menopause knowledge over time. Changes will be compared among the video-based education, Pecha Kucha-based education, and control groups. The findings will provide evidence regarding the effectiveness of the two educational approaches and help determine which method better supports safe and informed online health information-seeking during the menopausal transition.

Studietype

Ingrijpend

Inschrijving (Geschat)

60

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

45 jaar tot 65 jaar (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Vrouw

Beschrijving

Inclusion Criteria:

  • Aged 40 to 65 years
  • Being in the perimenopausal or postmenopausal period
  • Able to read and understand Turkish
  • Having experience using a smartphone, the internet, or social media
  • Willing to participate and able to provide informed consent

Exclusion Criteria:

  • Having a diagnosed psychiatric disorder
  • Having a neurological disorder that affects cognitive functioning
  • Having a hearing or visual impairment that prevents effective communication or participation
  • Having a severe health condition that prevents regular participation in the study

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Ander
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Video-Based Education Group

Participants will receive structured health information-seeking education delivered through a video.

Video-Based Health Information-Seeking Education: Participants will receive structured health information-seeking education through an educational video. The video will explain the benefits and risks of searching for health information online; how to assess the author, institution, publication date, and scientific basis of online content; how to recognize advertisements, commercial content, sensational headlines, and misleading social media information; how to use appropriate search terms and verify information across multiple reliable sources; and how to limit repetitive searches that may increase health-related anxiety. The video format allows the educational content to be delivered in a standardized audiovisual format.

Experimenteel: Pecha Kucha-Based Education Group

Participants will receive structured health information-seeking education delivered using the Pecha Kucha presentation format.

Pecha Kucha-Based Health Information-Seeking Education: Participants will receive structured health information-seeking education using the Pecha Kucha presentation format. The presentation will consist of 20 visually focused slides, each displayed automatically for

Geen tussenkomst: Control Group

Participants will not receive structured health information-seeking education during the study period. They will complete the assessments at the same time points as the intervention groups.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in Cyberchondria Severity Scale-Short Form Score
Tijdsspanne: Baseline, immediately after the intervention, and 1 month after the intervention

Cyberchondria will be assessed using the 12-item Cyberchondria Severity Scale-Short Form (CSS-12). The scale evaluates excessive online health searches, distress, reassurance seeking, and compulsive searching. Each item is rated on a 5-point scale. Total scores range from 12 to 60, with higher scores indicating greater cyberchondria severity. Changes in scores will be compared among the video-based education, Pecha Kucha-based education, and control groups.

Baseline, immediately after the intervention, and 1 month after the intervention

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in E-Health Literacy Scale Score
Tijdsspanne: Baseline, immediately after the intervention, and 1 month after the intervention

E-health literacy will be assessed using the E-Health Literacy Scale. The scale evaluates participants' perceived ability to find, understand, evaluate, and use health information obtained from electronic sources. The eight scored items are rated on a 5-point scale, producing a total score ranging from 8 to 40. Higher scores indicate greater e-health literacy. Changes in scores will be compared among the three study groups.

Baseline, immediately after the intervention, and 1 month after the intervention

Andere uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in Menopause Knowledge Scale Score
Tijdsspanne: Baseline, immediately after the intervention, and 1 month after the intervention

Knowledge about menopause will be assessed using the 14-item Menopause Knowledge Scale. The scale includes two domains: general menopause knowledge and knowledge of menopausal symptoms and their management. Total scores range from 14 to 70, with higher scores indicating greater menopause knowledge. Changes in scores will be compared among the three study groups.

Baseline, immediately after the intervention, and 1 month after the intervention

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

24 januari 2027

Primaire voltooiing (Geschat)

30 maart 2027

Studie voltooiing (Geschat)

1 juni 2027

Studieregistratiedata

Eerst ingediend

17 september 2026

Eerst ingediend dat voldeed aan de QC-criteria

17 september 2026

Eerst geplaatst (Werkelijk)

22 september 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

22 september 2026

Laatste update ingediend die voldeed aan QC-criteria

17 september 2026

Laatst geverifieerd

1 september 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

Individual participant data will not be shared with other researchers because the data contain personal health information and external data sharing is not included in the current study protocol and ethical approval. Study findings will be reported only in aggregate form to protect participant confidentiality.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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