The Effect of Cancer Awareness Web-Based Education in Schools
The Effect of Web-Based Cancer Awareness Education in Schools on Students' Knowledge Level, Help-Seeking Behaviors, and Stigma Attitudes
Objective: This study aims to determine the effect of web-based cancer awareness education in schools on students' knowledge levels, help-seeking attitudes, and stigma attitudes.
Method: The Web-Based Adolescent Cancer Education (WAKE) study was planned as a school-based, randomized controlled experimental study. Qualified high schools in the public sector of Izmir province will constitute the study population. Private schools are excluded for adolescents whose additional needs cannot be met in inclusive education. Two schools will be selected using a purposive sampling method (15-18 age group) and assigned to the experimental and control groups. This will prevent interaction between students in both schools. Students in each school will be listed, and assignments to groups will be made using a web-based randomizer application with randomly selected numbers (https://www.randomizer.org/). Data will be collected using the Cancer Awareness Scale (CAM), the Cancer Stigma Scale (CASS-T), and a Basic Demographic Questionnaire. In the evaluation of the data, descriptive statistics (number, percentage, and statistic) will be used, and repeated measures analysis of variance will be employed to assess the effect of the intervention. Differences in results between the experimental and control groups will be tested using multiple regression methods.
調査の概要
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究場所
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Izmir、トルコ（Türkiye）、35130
- Dokuz Eylül University Hospital
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参加基準
適格基準
就学可能な年齢
- 子
- 大人
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Being a student aged 15-18 in selected schools
- Volunteers who have withdrawn must agree to participate
- Parents must fill out an informed consent form
- Lack of literacy skills
Exclusion Criteria:
- Having a problem that will prevent communication
- Students who do not agree to the study
- Students whose parents' permission cannot be obtained
- Not being able to access and use the internet
- The student wants to voluntarily withdraw from the research
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：防止
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的：Web-Based Cancer Awareness Education
Students receive a web-based cancer awareness education program delivered in school settings, providing education on cancer awareness, help-seeking behaviors, and cancer-related stigma.
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A web-based educational program delivered in school settings that provides education on cancer-related knowledge, help-seeking behaviors, and cancer-related stigma.
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介入なし：No Cancer Awareness Education Control
Students do not receive the web-based cancer awareness education program during the study period.
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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Cancer Awareness Level
時間枠：Baseline (pre-intervention), immediately after the intervention, 1 month after the intervention, and 3 months after the intervention.
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Cancer Awareness Level: Cancer awareness will be assessed using the Cancer Awareness Measure (CAM).
The CAM measures multiple dimensions of cancer awareness, including awareness of cancer warning signs, cancer risk factors, and help-seeking behavior.
Total scores range from 0 to 77, with higher scores indicating greater cancer awareness.
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Baseline (pre-intervention), immediately after the intervention, 1 month after the intervention, and 3 months after the intervention.
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Cancer-Related Stigma Attitudes
時間枠：Baseline (pre-intervention), immediately after the intervention, 1 month after the intervention, and 3 months after the intervention.
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Cancer-related stigma attitudes will be assessed using the Cancer Stigma Scale-Turkish (CASS-T).
The scale measures attitudes toward individuals with cancer and cancer-related stigma.
Total scores range from 25 to 150, with higher scores indicating greater perceived stigma.
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Baseline (pre-intervention), immediately after the intervention, 1 month after the intervention, and 3 months after the intervention.
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協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- Institute of Health Sciences
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。