- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07655947
Theory of Planned Behavior-Based Digital Addiction and Screen Time Management Training for Teachers
The Impact of a Planned Behavior Theory-Based Digital Addiction and Screen Time Management Training on Teachers' Internet Addiction, Sleep Quality, and Psychological Well-being
This thesis focuses on problematic internet use, a widespread issue in contemporary society, and its negative effects on sleep quality and psychological well-being. The indispensable role of the internet in daily life and the risks associated with excessive use constitute an important area of research, particularly in relation to internalizing symptoms and health-related problems. Within this context, considering teachers' intensive engagement with digital media and their role as role models, the study aims to improve their awareness and behaviors regarding digital media use.
The aim of the thesis is to examine the effects of a Theory of Planned Behavior (TPB)-based Digital Addiction and Screen Time Management training program on levels of internet addiction, sleep quality, and psychological well-being among middle school teachers in Aydın province, using a randomized controlled experimental design.
In terms of methodology, a total of 102 teachers-51 in the intervention group and 51 in the control group-will be assessed before and after the training. Data will be collected using a Personal Information Form, the Young Internet Addiction Test-Short Form, the Pittsburgh Sleep Quality Index, and the Psychological Well-Being Scale.
The expected outcomes are that the implemented training will significantly reduce teachers' levels of internet addiction, improve their sleep quality, and lead to improvements in psychological well-being. These findings are expected to contribute to teachers' health and to provide guidance for the development of similar intervention programs for other populations.
Studienübersicht
Status
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Aydın
-
Efeler, Aydın, Türkei (türkiye)
- AydınAdnan Menderes University, Faculy of Nursing, Division Public Health Nursing
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
Teachers who voluntarily agree to participate in the study and provide written informed consent.
- Teachers who regularly use digital devices and the internet in their daily lives.
Exclusion Criteria:
- Teachers who are receiving medical treatment or psychological support due to digital addiction, sleep disorders, or psychological conditions.
- Teachers who are unable to attend the training program on a regular basis.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Versorgungsforschung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: experimental group
The teachers in the experimental group were provided with Digital Addiction and Screen Time Management Trainings based on the Theory of Planned Behavior, which were developed by the researchers through literature review and expert opinions.
|
The Digital Addiction and Screen Time Management Training Based on the Theory of Planned Behavior was implemented over a period of six weeks.
|
|
Experimental: Control group
The control group received no intervention.
|
The control group received no intervention.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Personal Information Form
Zeitfenster: Baseline, immediately after intervention, 3 month after intervention.
|
The form, prepared by the researchers, consists of 9 questions created in line with the literature review, covering general information about the teachers' socio-demographic characteristics.
|
Baseline, immediately after intervention, 3 month after intervention.
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Young Internet Addiction Test-Short Form
Zeitfenster: Baseline, immediately after intervention, 3 month after intervention.
|
The scale was originally developed by Young, and its short form was later created by Pawlikowski, Altstötter-Gleich, and Brand.
The scale is a 12-item, unidimensional, 5-point Likert-type scale (scored from 1 to 5).
The Turkish adaptation of the scale was carried out by Kutlu and colleagues.
The total score ranges from 12 to 60, with no reverse-coded items or cut-off point.
Higher scores on the scale indicate a higher level of internet addiction in the individual.
While the Cronbach's Alpha internal consistency coefficient of the YIAT-SF scale was 0.85, this value was calculated as 0.89 in this study.
|
Baseline, immediately after intervention, 3 month after intervention.
|
Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Pittsburgh Sleep Quality Index (PSQI)
Zeitfenster: Baseline, immediately after intervention, 3 month after intervention.
|
Developed by Buysse et al. (1989), PSQI measures sleep quality/problems over the past month.
Cronbach's alpha = 0.80; validity confirmed via test-retest.
Turkish adaptation by Ağargün et al. (1996) also showed α = 0.80, confirming psychometric stability.
Total 24 items: 19 self-reported, 5 based on spouse/roommate observations (clinical use only; roommate item excluded from scoring).
Scoring uses 18 items across 7 components, each item 0-3.
Total score 0-21; ≥5 = clinically significant.
Components: Subjective Sleep Quality (item 6), Sleep Latency (items 2+5a), Sleep Duration (item 4), Sleep Efficiency (items 1+3+4), Sleep Disturbances (5b-5j), Medication Use (item 7), Daytime Dysfunction (items 8+9).
Item 4 is used for both Sleep Duration and Sleep Efficiency, a key design feature.
|
Baseline, immediately after intervention, 3 month after intervention.
|
|
Psychological Well-Being Scale
Zeitfenster: Baseline, immediately after intervention, 3 month after intervention.
|
Diener and colleagues (2009) developed a measurement tool to assess individuals' socio-psychological health status (Diener et al., 2010).
This scale was later adapted to Turkish culture by Telef (2013) and transformed into an 8-item form (Telef et al., 2013).
In the analyses conducted, the factor loadings of the scale items were found to range between 0.54 and 0.76.
As a result of the reliability analyses of the scale, the Cronbach's alpha coefficient was calculated as 0.80.
It was determined that the item-total correlation coefficients ranged between 0.41 and 0.63, and the t-test results were statistically significant (p < 0.001).
The response options used in the scale have a seven-point Likert-type structure: "Strongly disagree," "Disagree," "Slightly disagree," "Undecided," "Slightly agree," "Agree," and "Strongly agree.
|
Baseline, immediately after intervention, 3 month after intervention.
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- Digital Addiction
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
IPD-Sharing-Zeitrahmen
IPD-Sharing-Zugriffskriterien
Art der unterstützenden IPD-Freigabeinformationen
- CSR
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .