- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07663981
The Effect of Peer-Guided Education on Organ Donation on Organ Donation Attitude
18. Juni 2026 aktualisiert von: Gülsüm ÖZCAN ÇETİNER, Suleyman Demirel University
This research will be conducted to determine the effect of peer-guided organ donation education given to anesthesia students on their attitudes towards organ donation.
Studienübersicht
Status
Abgeschlossen
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
There are many people waiting for organ donation in our country.
Therefore, it is important to develop a positive attitude towards organ donation in our society.
This study was planned to determine the effect of peer-guided organ donation education to be given to anesthesia students on the attitude towards organ donation.
In the study, anesthesia students will be informed about organ donation.
It was thought that the education given towards organ donation will develop a positive attitude in students.
Studientyp
Interventionell
Einschreibung (Tatsächlich)
46
Phase
- Unzutreffend
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
-
-
Isparta
-
Isparta, Isparta, Türkei (türkiye), 32200
- Suleyman Demirel University
-
-
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Kind
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Ja
Beschreibung
Inclusion Criteria:
- Being 17 years of age or older, studying in the program in which the research is conducted, and agreeing to participate in the research voluntarily.
Exclusion Criteria:
- Having received prior training on organ donation
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Verhütung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: Educational intervention
The educational intervention consists of a two-hour program prepared by the peer student in line with the literature.
The training session was planned to be completed in four sessions, with 30 minutes of session time.
These four sessions cover the traditional education model with the help of slide presentation.
The content of the training model was planned to use techniques such as participant activity, group work and discussion, and a brochure prepared by the researcher.
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The training on organ donation will be conducted under peer guidance.
The training will be implemented using face-to-face lectures, slide presentations, brochures and group discussions.
It will be conducted at Süleyman Demirel University in the 2025-2026 academic year for first-year anesthesia students.
The content of the training includes the concept of organ donation, the conditions for becoming a donor (physical, legal, religious), the social dimension of organ donation and attitude development sessions through group discussions.
The training, planned in four sessions, will last two hours in total.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Change in "Organ Donation Attitude Scale" Positive Attitude Sub-dimension Score
Zeitfenster: Baseline, immediately after completion of the 4-week training program (Week 4), and 1 month after completion of the training program (Week 8).
|
The Organ Donation Attitude Scale was originally developed by Parisi and Kanz (1986) and later adapted to 46 items by Kent and Owens (1995).
The Turkish validity and reliability study was conducted by Yazıcı Sayın (2016).
After removing items 6, 7, 12, 19, 27, and 45, the final version consists of 40 items rated on a 6-point Likert scale (from "strongly agree" to "strongly disagree") and includes two subscales.
TThe Positive Attitude Subscale of the Organ Donation Attitude Scale consists of 20 items assessing altruism and moral values and beliefs related to organ donation.
Each item is rated on a 6-point Likert scale.
The total subscale score ranges from 20 to 120.
Higher scores indicate a more positive attitude toward organ donation and therefore represent a better outcome.
Change in scores will be evaluated across the three assessment time points.
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Baseline, immediately after completion of the 4-week training program (Week 4), and 1 month after completion of the training program (Week 8).
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Change in "Organ Donation Attitude Scale" Negative Attitude Sub-dimension Score
Zeitfenster: Baseline, immediately after completion of the 4-week training program (Week 4), and 1 month after completion of the training program (Week 8).
|
The Organ Donation Attitude Scale was originally developed by Parisi and Kanz (1986) and later adapted to 46 items by Kent and Owens (1995).
The Turkish validity and reliability study was conducted by Yazıcı Sayın (2016).
After removing items 6, 7, 12, 19, 27, and 45, the final version consists of 40 items rated on a 6-point Likert scale (from "strongly agree" to "strongly disagree") and includes two subscales.
The Negative Attitude Subscale of the Organ Donation Attitude Scale consists of 20 items assessing fear of medical neglect and fear of bodily injury related to organ donation.
Each item is rated on a 6-point Likert scale.
The total score ranges from 20 to 120.
Higher scores indicate a more negative attitude toward organ donation and represent a worse outcome.
Changes in the Negative Attitude Subscale score will be evaluated at baseline, immediately after the training program, and at the 1-month follow-up.
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Baseline, immediately after completion of the 4-week training program (Week 4), and 1 month after completion of the training program (Week 8).
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Change in organ/tissue donation knowledge, awareness, and donation intention item scores
Zeitfenster: Baseline, immediately after completion of the 4-week training program (Week 4), and 1 month after completion of the training program (Week 8).
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Participants' knowledge, awareness, and intention regarding organ/tissue donation were assessed using items included in the researcher-developed organ/tissue donation knowledge and attitude form.
These items evaluated participants' perceived level of knowledge about organ/tissue donation, knowledge of the required steps to become an organ/tissue donor, intention to donate organs/tissues, and perceived access to reliable sources of information about organ donation.
Each item was scored using Likert-type response options.
Higher scores indicated a more positive level of knowledge, awareness, or donation intention for the relevant item.
Changes in item scores were evaluated across the pre-test, post-test, and follow-up measurements.
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Baseline, immediately after completion of the 4-week training program (Week 4), and 1 month after completion of the training program (Week 8).
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Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Ermittler
- Studienleiter: Gulsum OZCAN CETINER, Lecturer, Suleyman Demirel University
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Tatsächlich)
20. November 2025
Primärer Abschluss (Tatsächlich)
11. Dezember 2025
Studienabschluss (Tatsächlich)
25. Januar 2026
Studienanmeldedaten
Zuerst eingereicht
3. Juli 2025
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
18. Juni 2026
Zuerst gepostet (Tatsächlich)
23. Juni 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
23. Juni 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
18. Juni 2026
Zuletzt verifiziert
1. Juni 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 2025/95 (MTÜ Health Sciences Ethics Committee)
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
NEIN
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Nein
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
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