ClinicalTrials.gg
CompletedNCT07693582Updated Jul 9, 2026

Smartphone-Based Digital Literacy Training for Older Adults

An interventional study of Structured smartphone-based digital literacy training in Aging, Literacy-language Intervention and Literacy, sponsored by Akdeniz University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 60 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-09.

Sponsored by Akdeniz University · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 2 months after the study started (first participant enrolled Apr 2025, registered Jul 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
140
Allocation
Non-randomized
Ages
60 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Aging
  • Literacy-language Intervention
  • Literacy
  • Older Adults (60 - 85 Years Old)

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Keywords

  • digital literacy
  • smartphone
  • ehealth
  • gerontology
  • lifelong learning
03

In context

Literacy

201 studies on the registry are indexed under Literacy; 69 are open to participants now.

This study's enrollment of 140 is above the median of 124 across 170 interventional studies indexed under Literacy.

Browse Literacy studies →

Lead sponsor

Akdeniz University is the lead sponsor of 297 studies on the registry; 62 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion criteria

Exclusion Criteria:

  • Severe cognitive, visual, or hearing impairment that would prevent participation in the training
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
140 participants (actual)

Study arms

  • Experimental
    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.

    Behavioral: Structured smartphone-based digital literacy training

  • No intervention
    Wait-list control

    Second-year cohort continuing usual programme activities with the training deferred; served as the comparison group.

Interventions

  • BehavioralStructured smartphone-based digital literacy training

    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.

06

What researchers measure

Primary outcomes

  1. Change in Digital Literacy Scale (DLS) score

    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).

    Time frame: Baseline (T1), immediately post-intervention (approximately week 6, T2), and 3-month follow-up (T3)

Secondary outcomes

  1. Change in Smartphone Self-Efficacy Scale (SSES) score

    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).

    Time frame: Baseline (T1), immediately post-intervention (approximately week 6, T2), and 3-month follow-up (T3)

  2. Programme satisfaction

    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).

    Time frame: Immediately post-intervention (approximately week 6, T2)

07

Study locations

1 site
  • Akdeniz University 60+ Tazelenme University
    Antalya, 07070, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: Yes — 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.

Supporting information: Analytic code

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

Access criteria: 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.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Apr 2025 to primary completion in Aug 2025, 4 months.

Of 115 non-industry interventional studies with no phase under Literacy, half reached primary completion within 11 months of starting (the median), counting those still running; a quarter within 4 and three quarters within 20. This study's 4 months is below that.

Counting every sponsor, half of 117 studies reached it within 11 months; a quarter within 4 and three quarters within 19.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 4, 2026
First posted
Jul 9, 2026
StartActual
Apr 15, 2025
Primary completionActual
Aug 22, 2025
CompletionActual
Aug 22, 2025
Last update
Jul 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07693582
Lead sponsor
Akdeniz University
Responsible party
Barış Kılıç (Research Assistant, Principal Investigator, Akdeniz University) — Principal investigator
First posted
Jul 9, 2026
Start date
Apr 15, 2025
Primary completion
Aug 22, 2025
Completion
Aug 22, 2025
Last update
Jul 9, 2026

Study contacts

Gülüşan Özgün Başıbüyük
study director · Akdeniz University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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