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Not yet recruiting NCT07570797

Mentor-Supported Digital Literacy Training

No phase Interventional eHealth Literacy Digital Literacy Migrants

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: MEDOYE, control grup.
Who it may be relevant to
Registry conditions: eHealth Literacy, Digital Literacy, Migrants. Basic parameters: 18 years — 74 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effects of Digital Literacy Mentoring Delivered by Young Migrants on eHealth and Digital Literacy Among Older Migrants: A Randomized Controlled Trial

Overview

Purpose This study is a randomized controlled experimental trial aiming to evaluate the effects of mentoring-based digital literacy training delivered by young migrants on older migrants' eHealth literacy and their ability to seek and verify health information in digital environments. The study will be conducted among young and older Ahiska Turkish migrants living in the Üzümlü district of Erzincan province. Method The study will be conducted in two phases. In the first phase, young migrants will receive digital literacy training that includes mentoring skills. In the second phase, these individuals will provide training to older migrants. The sample size has been determined based on a power analysis and will consist of a total of 80 participants. Data will be collected using the eHealth Literacy Scale and the Digital Health Information Seeking and Verification Scale. Data will be analyzed using SPSS software, and appropriate parametric and/or non-parametric tests will be applied. Training sessions will be conducted in controlled environments, in small groups, and tailored to participants' needs. Participant follow-up will be maintained throughout the process to support the sustainability of the intervention. Research Hypotheses Primary Hypothesis * H0: Mentoring-based digital literacy training delivered by young migrants has no effect on older migrants' levels of eHealth literacy and digital literacy. * H1: Mentoring-based digital literacy training delivered by young migrants has a significant effect on older migrants' levels of eHealth literacy and digital literacy. Secondary Hypothesis * H0: Mentoring-based digital literacy training delivered by young migrants has no effect on older migrants' eHealth literacy levels. * H2: Mentoring-based digital literacy training delivered by young migrants has a significant effect on older migrants' eHealth literacy levels. Third Hypothesis * H0: Mentoring-based digital literacy training delivered by young migrants has no effect on older migrants' digital literacy levels. * H3: Mentoring-based digital literacy training delivered by young migrants has a significant effect on older migrants' digital literacy levels.

Interventions

  • Other MEDOYE
    Participants who agree to take part in the study will be enrolled in a mentoring-based training program. The training content will include group process management, warm-up activities, computer-assisted instruction (PowerPoint presentations), verbal instruction, role-playing, demonstration and practice, small group discussions, and question-answer techniques. A total of nine training sessions will be conducted twice a week, each lasting 45-90 minutes. Short breaks not exceeding 15 minutes will
  • Other control grup
    Participants in the control group will receive no intervention during the study period. At baseline, participants will complete the pre-test assessments, including the Personal Information Form, the eHealth Literacy Scale, and the Digital Health Information Seeking and Verification Scale. After the completion of the experimental group intervention, post-test assessments will be administered. Following the study, digital literacy training will also be provided to control group participants.

Primary outcome measures

  • eHealth Literacy Scale [Time frame: Baseline and 6 weeks after intervention]
Secondary outcome measures (1)
  • Digital Health Information Seeking and Verification Scale [Time frame: Baseline and 6 weeks after intervention]

Eligibility criteria

Inclusion Criteria:Young Participants (Migrants)

  • Aged between 18-64 years
  • Being a migrant
  • Literate (able to read and write)
  • Able to speak and write in Turkish
  • Able to communicate verbally
  • Having access to internet at home or workplace
  • Having access to a smartphone or a phone that belongs to a family member and can be used by the participant
  • Able to use the internet
  • Willing to participate in the study
  • Willing to act as a mentor

Older Participants (Migrants)

  • Aged between 65-74 years
  • Literate in Turkish
  • Having internet access at home
  • Using a smartphone

Exclusion criteria

Young Participants (Migrants)

  • Presence of visual or hearing impairments that would prevent participation in the study
  • Having a physical or mental health condition that may interfere with participation
  • Inability to attend training sessions regularly during the intervention period

Older Participants (Migrants)

  • Presence of visual or hearing impairments that would prevent participation in the study
  • Inability to attend training sessions regularly during the intervention period

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07570797 · 24

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗