- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07693582
Smartphone-Based Digital Literacy Training for Older Adults
Smartphone-based Digital Literacy Training for Older Adults in a Lifelong-learning Setting: a Nonrandomised Wait-list-controlled Study With 3-month Follow-up
Study Overview
Status
Intervention / Treatment
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.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Antalya, Turkey (Türkiye), 07070
- Akdeniz University 60+ Tazelenme University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
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.
|
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.
|
|
No Intervention: Wait-list control
Second-year cohort continuing usual programme activities with the training deferred; served as the comparison group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Digital Literacy Scale (DLS) score
Time Frame: 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)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Smartphone Self-Efficacy Scale (SSES) score
Time Frame: 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
Time Frame: 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)
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Gülüşan Özgün Başıbüyük, Akdeniz University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- TBAEK-181
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- ANALYTIC_CODE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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