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.
Tutkimuksen yleiskatsaus
Tila
Opintotyyppi
Ilmoittautuminen (Todellinen)
Vaihe
- Ei sovellettavissa
Yhteystiedot ja paikat
Opiskelupaikat
-
-
Aydın
-
Efeler, Aydın, Turkki (Türkiye)
- AydınAdnan Menderes University, Faculy of Nursing, Division Public Health Nursing
-
-
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
- Aikuinen
Hyväksyy terveitä vapaaehtoisia
Kuvaus
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.
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Terveyspalvelututkimus
- Jako: Satunnaistettu
- Inventiomalli: Rinnakkaistehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
|
Kokeellinen: 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.
|
|
Kokeellinen: Control group
The control group received no intervention.
|
The control group received no intervention.
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Personal Information Form
Aikaikkuna: 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.
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Young Internet Addiction Test-Short Form
Aikaikkuna: 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.
|
Muut tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Pittsburgh Sleep Quality Index (PSQI)
Aikaikkuna: 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
Aikaikkuna: 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.
|
Yhteistyökumppanit ja tutkijat
Sponsori
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Todellinen)
Ensisijainen valmistuminen (Todellinen)
Opintojen valmistuminen (Todellinen)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Muita asiaankuuluvia MeSH-ehtoja
- Teknologiariippuvuus
- Käyttäytyminen, riippuvuutta aiheuttava
- Pakonomaista käyttäytymistä
- Impulsiivinen käyttäytyminen
- Käyttäytyminen
- Henkilökohtainen tyytyväisyys
- Internet-riippuvuushäiriö
- Psykologinen hyvinvointi
- Tutkintatekniikat
- Epidemiologinen tutkimussuunnittelu
- Epidemiologiset menetelmät
- Tutkimussuunnittelu
- Menetelmät
- Kontrolliryhmät
Muut tutkimustunnusnumerot
- Digital Addiction
Yksittäisten osallistujien tietojen suunnitelma (IPD)
Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?
IPD-suunnitelman kuvaus
IPD-jaon aikakehys
IPD-jaon käyttöoikeuskriteerit
IPD-jakamista tukeva tietotyyppi
- CSR
Lääke- ja laitetiedot, tutkimusasiakirjat
Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta
Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta
Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .