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Smartphone-Based Digital Literacy Training for Older Adults

8. juli 2026 opdateret af: Barış Kılıç, Akdeniz University

Smartphone-based Digital Literacy Training for Older Adults in a Lifelong-learning Setting: a Nonrandomised Wait-list-controlled Study With 3-month Follow-up

This study examined whether a structured, classroom-based smartphone training programme can improve digital literacy and confidence in using a smartphone among adults aged 60 years and older enrolled in a lifelong-learning programme. The study used a non-randomised, wait-list-controlled design with two existing class cohorts: one cohort received the training first (intervention group), and the other continued with its usual programme activities and served as a comparison (wait-list control group). Digital literacy and smartphone self-efficacy were measured before the training, immediately after the training, and again three months later. The aim was to determine whether older adults who took part in the training showed greater improvement than those who did not.

Studieoversigt

Detaljeret beskrivelse

The training programme consisted of 12 sessions delivered over 6 weeks (two sessions per week, each lasting 90 to 105 minutes). Content was mapped to the DigComp 2.2 digital competence framework and covered practical smartphone skills for everyday life. Sessions used participants' own Android smartphones together with a projector for demonstration, a class messaging group for support, and between-session practice tasks. The intervention arm comprised the advanced-level cohort of the Akdeniz University 60+ Refresher (Tazelenme) University, and the wait-list control arm comprised the second-year cohort of the same programme.

Two instruments were used. Digital literacy was assessed with the Digital Literacy Scale (score range 12 to 60), the primary outcome. Smartphone self-efficacy was assessed with the Smartphone Self-Efficacy Scale (score range 20 to 100), a secondary outcome. Both were administered at baseline (T1), immediately after the intervention (T2), and at three-month follow-up (T3). Programme satisfaction was assessed with a short questionnaire after the intervention.

The primary analysis used a baseline-adjusted linear mixed model on the full analysis set, including a group-by-baseline interaction and adjustment for age, sex, education, and marital status. Robustness was examined through several pre-specified sensitivity analyses, including per-protocol analysis, difference-in-differences, propensity-score overlap weighting, multiple imputation, and a conservative worst-case (missing-not-at-random) analysis.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

140

Fase

  • Ikke anvendelig

Kontakter og lokationer

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

Studiesteder

      • Antalya, Tyrkiet (Türkiye), 07070
        • Akdeniz University 60+ Tazelenme 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

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • Aged 60 years or older
  • Enrolled in the Akdeniz University 60+ Refresher (Tazelenme) University programme
  • Owns and regularly uses an smartphone
  • Able to attend the scheduled training sessions
  • Provides written informed consent

Exclusion Criteria:

  • Severe cognitive, visual, or hearing impairment that would prevent participation in the training

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Andet
  • Tildeling: Ikke-randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Smartphone-based digital literacy training
Advanced-level cohort receiving a structured smartphone training programme: 12 sessions over 6 weeks (two sessions per week, 90 to 105 minutes each), mapped to the DigComp 2.2 framework, using participants' own Android smartphones.
Instructor-led smartphone training delivered in 12 sessions over 6 weeks (twice weekly, 90 to 105 minutes), mapped to the DigComp 2.2 framework, using participants' own Android smartphones, a projector for demonstration, a class messaging group, and between-session practice tasks.
Ingen indgriben: Wait-list control
Second-year cohort continuing usual programme activities with the training deferred; served as the comparison group.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in Digital Literacy Scale (DLS) score
Tidsramme: Baseline (T1), immediately post-intervention (approximately week 6, T2), and 3-month follow-up (T3)
Digital literacy assessed with the Digital Literacy Scale. Scores range from a minimum of 12 to a maximum of 60. Higher scores indicate greater digital literacy (a better outcome).
Baseline (T1), immediately post-intervention (approximately week 6, T2), and 3-month follow-up (T3)

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in Smartphone Self-Efficacy Scale (SSES) score
Tidsramme: Baseline (T1), immediately post-intervention (approximately week 6, T2), and 3-month follow-up (T3)
Smartphone self-efficacy assessed with the Smartphone Self-Efficacy Scale. Scores range from a minimum of 20 to a maximum of 100. Higher scores indicate greater smartphone self-efficacy (a better outcome).
Baseline (T1), immediately post-intervention (approximately week 6, T2), and 3-month follow-up (T3)
Programme satisfaction
Tidsramme: Immediately post-intervention (approximately week 6, T2)
Participant satisfaction with the training programme, assessed with a 10-item satisfaction questionnaire. Scores range from a minimum of 10 to a maximum of 50. Higher scores indicate greater satisfaction (a better outcome).
Immediately post-intervention (approximately week 6, T2)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Studieleder: Gülüşan Özgün Başıbüyük, Akdeniz University

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)

15. april 2025

Primær færdiggørelse (Faktiske)

22. august 2025

Studieafslutning (Faktiske)

22. august 2025

Datoer for studieregistrering

Først indsendt

4. juli 2026

Først indsendt, der opfyldte QC-kriterier

8. juli 2026

Først opslået (Faktiske)

9. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

9. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

8. juli 2026

Sidst verificeret

1. juli 2026

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • TBAEK-181

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

JA

IPD-planbeskrivelse

De-identified individual participant data underlying the reported results are available from the corresponding author (B.K.) on reasonable request, subject to ethics and participant-confidentiality restrictions. The analysis code is likewise available from the corresponding author on reasonable request.

IPD-delingstidsramme

Available beginning after publication of the main results, with no fixed end date.

IPD-delingsadgangskriterier

Requests are reviewed by the corresponding author (B.K.). De-identified data and analytic code will be shared with researchers who submit a methodologically sound proposal and sign a data-access and confidentiality agreement, subject to applicable ethics approvals and participant-confidentiality restrictions.

IPD-deling Understøttende informationstype

  • ANALYTIC_CODE

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Ingen

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