- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07706738
DIGITAL FOOTPRINT EDUCATION PROGRAM FOR PARENTS
July 10, 2026 updated by: Şeyma Emsal Şen, Akdeniz University
YOUR CHILD'S DIGITAL IDENTITY IS SHAPED BY YOUR FINGERSTIPS: EFFECTIVENESS OF A DIGITAL FOOTPRINT EDUCATION PROGRAM FOR PARENTS
In today's digitalized world, children conduct a significant portion of their learning experiences through online environments.
However, a lack of digital awareness among parents can adversely affect both children's privacy and their educational development.
To address this issue, this study aims to support children's development within a conscious, safe, and ethical digital learning environment by educating parents on digital footprints, online safety, and responsible sharing.
Children, who are not yet capable of constructing their own digital identities, have their virtual personas shaped at an early age by their parents' online behavior.
This unmonitored digital exposure can compromise a child's sense of privacy and negatively impact their self-development, self-esteem, and social identity formation.
Prioritizing the best interests of the child, this project introduces a parent education program designed to empower families in digital literacy and establish an indirect protective framework throughout the educational process.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Digital footprints represent the permanent traces that individuals leave behind in online environments, either consciously or unconsciously.
Today, social media stands out as one of the platforms where these footprints are most intensively generated.
As one of the most active user groups on social media, parents frequently share photos, videos, and personal information about their children, directly impacting their privacy, digital safety, and psychosocial development.
Furthermore, this behavior creates a negative role model, leading children to adopt unconscious digital habits from their parents.
This unmonitored exposure increases the likelihood of children facing risks such as abuse, cyberbullying, and labeling in digital spaces, thereby threatening their psychosocial safety within school and learning environments.At this juncture, enhancing parents' digital awareness is critically important for both ensuring children's online safety and safeguarding their healthy development throughout the educational process.
Designed within this framework, this project introduces a parent education program that prioritizes the best interests of the child, empowers families in digital literacy, and serves as an indirect protective shield in the educational process.
In this regard, the study closely aligns with children's academic and psychosocial development goals by both contributing to family education and enhancing the safety of educational environments.
The "Digital Footprint Education Program," developed within this scope, aims to raise parents' awareness regarding social media and online sharing practices, while enabling them to cultivate attitudes that protect their children's digital identity and privacy.
Study Type
Interventional
Enrollment (Actual)
79
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Antalya, Turkey (Türkiye)
- Antalya, Konyaalti
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being the parent of a child enrolled in kindergarten,
- The parent uses social media
- The parent uses WhatsApp
- The parent is literate
- The parent can speak and understand Turkish
Exclusion Criteria:
- The parent has a diagnosed psychiatric or mental disorder.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Intervention group
The startup group was given training as part of the digital footprint training program.
|
A review of the literature reveals a paucity of research focusing on children aged 3-6, with existing scholarship predominantly centered on primary school students and older cohorts.
Implemented with the parents of children aged 3-6 within the intervention group, this educational program aims to favorably modulate the digital footprints of this specific age bracket and safeguard their digital identities.
In this regard, the intervention diverges significantly from extant literature.
Other Names:
|
|
No Intervention: control group
No action was taken against this group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sharenting scale
Time Frame: Baseline and 15 days after the intervention
|
The Sharenting Scale is a 17-item instrument designed to assess parental sharenting behaviors.
The scale comprises four subscales: sharing behavior, social comparison behavior, positive feedback effect, and negative feedback effect.
Items are rated on a 5-point Likert scale, and the items in the social comparison behavior and negative feedback effect subscales are reverse scored.
Total scores range from 17 to 85, with higher scores indicating greater levels of sharenting behaviors.
|
Baseline and 15 days after the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Social Media Addiction Scale
Time Frame: Baseline and 15 days after the intervention
|
The Social Media Addiction Scale is a 13-item instrument designed to assess the level of social media addiction in adults.
The scale includes three subscales: functional impairment, preference for virtual life, and virtual pleasure.
Each item is rated on a 5-point Likert scale ranging from 1 (strongly disagree) to 5 (strongly agree).
Total scores range from 13 to 65, with higher scores indicating greater levels of social media addiction.
|
Baseline and 15 days after the intervention
|
|
Brief Self-Control Scale
Time Frame: Baseline and 15 days after the intervention
|
The Brief Self-Control Scale is a 13-item self-report instrument designed to assess self-control.
The scale consists of two subscales: self-discipline and impulsivity.
Items are rated on a 5-point Likert scale ranging from 1 (not at all like me) to 5 (very much like me).
Nine items are reverse scored.
Total scores range from 13 to 65, with higher scores indicating greater levels of self-control.
|
Baseline and 15 days after the intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Sarkadi A, Dahlberg A, Fangstrom K, Warner G. Children want parents to ask for permission before 'sharenting'. J Paediatr Child Health. 2020 Jun;56(6):981-983. doi: 10.1111/jpc.14945. No abstract available.
- Steinberg, S. (2017). Sharenting: Children's privacy in the age of social media. Emory Law Journal, 66(4), 839-884.
- Talukdar, N. (2020). The adverse effects of family vlogging on children. International Journal of Research and Analytical Reviews, 7(1), 749-756.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 15, 2026
Primary Completion (Actual)
April 15, 2026
Study Completion (Actual)
May 15, 2026
Study Registration Dates
First Submitted
July 6, 2026
First Submitted That Met QC Criteria
July 10, 2026
First Posted (Actual)
July 16, 2026
Study Record Updates
Last Update Posted (Actual)
July 16, 2026
Last Update Submitted That Met QC Criteria
July 10, 2026
Last Verified
July 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- sesen
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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