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Health Belief Model-Based Breast Self-Examination Education in University Students

30. september 2026 opdateret af: Esma Demirezen, Istanbul University - Cerrahpasa

The Effect of Health Belief Model-Based Breast Self-Examination Education on the Precaution Adoption Process Among University Students

This study aims to evaluate the effect of Health Belief Model-based breast self-examination education on the precaution adoption process among university students who have never performed breast self-examination. Participants are assigned to intervention and control groups. The intervention group receives Health Belief Model-based education on breast health and breast self-examination, while the control group does not receive this education during the study period. The study examines whether the educational intervention promotes progression through the stages of the Precaution Adoption Process Model and influences health beliefs related to breast self-examination.

Studieoversigt

Status

Aktiv, ikke rekrutterende

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

110

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Istanbul
      • Istanbul, Istanbul, Tyrkiet (Türkiye), 34403
        • Istanbul Atlas University

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Barn
  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Kvinde

Beskrivelse

Inclusion Criteria:

  • Female university students
  • Able to understand and communicate in Turkish
  • Voluntary participation in the study
  • Have never performed breast self-examination (BSE)

Exclusion Criteria:

  • Unable to understand or communicate in Turkish
  • Unwilling to participate in the study

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Health Belief Model-Based Education Group

Participants in this arm receive Health Belief Model-based education on breast health and breast self-examination.

Participants in the intervention group receive Health Belief Model-based education on breast health and breast self-examination. The educational intervention is designed to improve health beliefs related to breast self-examination and facilitate progression through the stages of the Precaution Adoption Process Model.

Ingen indgriben: Control Group

Participants in this arm do not receive the Health Belief Model-based breast self-examination education during the study period.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Precaution Adoption Process Model Stage for Breast Self-Examination
Tidsramme: Approximately 1 month after the intervention

The Precaution Adoption Process Model (PAPM) is used to assess participants' stage of adoption of breast self-examination (BSE) approximately one month after the intervention. PAPM stage is assessed using a single-choice staging question adapted to BSE. Participants select the statement that best describes their current status regarding BSE and are classified into one of seven stages: (1) never performed BSE, (2) aware of BSE but has not considered it personally relevant or necessary, (3) undecided about performing BSE, (4) decided not to perform BSE, (5) decided to perform BSE but has not yet started, (6) started performing BSE within the last six months but does not yet perform it regularly, or (7) regularly performs BSE, defined as at least once per month during the last six months. The outcome is reported as the number and percentage of participants in each PAPM stage, and the distribution of stages is compared between the intervention and control groups.

Approximately 1 month after the intervention

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in Health Beliefs Related to Breast Self-Examination Assessed Using the Champion Health Belief Model Scale
Tidsramme: Baseline and approximately 1 month after the intervention

Health beliefs related to breast self-examination (BSE) are assessed using Karayurt's Turkish adaptation of the Champion Health Belief Model Scale. The scale consists of 42 items rated on a 5-point Likert scale ranging from 1 (strongly disagree) to 5 (strongly agree), and each subscale is scored separately. The subscales and possible score ranges are: susceptibility (3-15), seriousness (7-35), perceived benefits of BSE (4-20), perceived barriers to BSE (11-55), BSE self-efficacy/confidence (10-50), and health motivation (7-35). Higher scores indicate higher levels of the corresponding construct. Thus, higher susceptibility, seriousness, perceived benefits, self-efficacy/confidence, and health motivation scores indicate higher levels of these beliefs, whereas higher perceived barriers scores indicate greater perceived barriers to BSE. Changes in each subscale score from baseline to approximately one month after the intervention are compared between the intervention and control groups.

Baseline and approximately 1 month after the intervention

Samarbejdspartnere og efterforskere

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Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

18. februar 2026

Primær færdiggørelse (Anslået)

20. oktober 2026

Studieafslutning (Anslået)

20. oktober 2026

Datoer for studieregistrering

Først indsendt

24. september 2026

Først indsendt, der opfyldte QC-kriterier

30. september 2026

Først opslået (Faktiske)

1. oktober 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

1. oktober 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

30. september 2026

Sidst verificeret

1. september 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

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Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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