The Effect of Mosaic Puzzle Game on Nomophobia in Adolescents

NCT ID: NCT07097610

Last Updated: 2025-07-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-02-15

Study Completion Date

2025-05-25

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study aims to investigate the effect of mosaic puzzle application on nomophobia in middle school children aged 12-14.

The data for the study will be collected over a 5-week period. The experimental group children will be asked to play mosaic puzzle games for 1 hour, 2 days a week for 5 weeks, at a time deemed appropriate by the school and under the supervision of the researcher. The control group children will not be given any intervention; they will only be observed, and a final test will be administered at the end of the 5 weeks. The study is planned as a single-center study, and a total of 30 children aged 12-14 with a nomophobia scale score of 60 or higher who meet the inclusion criteria will be included in the study.

Hypothesis 1: The intervention group's level of nomophobia is lower than that of the control group.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Nomophobia Puzzle Activity Child Dependence Smart Phone Addiction

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

nomophobia child dependence smart phone addiction puzzle activity

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The study includes one intervention group and one control group.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Experimental: "Mosaic Puzzle Intervention Group"

Arm Description: In the study, the child's level of nomophobia will first be determined using a Personal Information Form and a nomophobia measurement tool. Subsequently, the mosaic puzzle intervention will be administered to the children in the experimental group twice a week for one hour over a period of five weeks, at times deemed appropriate by the school, and will be monitored by the researcher.

Mosaic Puzzle Initiative A mosaic puzzle is the process of creating a picture or image by putting together small crystal stones. It involves sticking the appropriate crystal stones onto a canvas painting using wax and a wax pencil, matching them with the symbols (letters, numbers, shapes, etc.) shown on the painting. (e.g., sticking blue crystal stones gathered under the \* symbol onto the square marked with \* on the canvas). The student presses the wax pencil onto the wax to pick up a small amount of wax. Then, they press the wax-coated pencil onto the crystal stone and stick it onto the

Group Type EXPERIMENTAL

Mosaic Puzzle Intervention

Intervention Type OTHER

This study aims to investigate the effect of mosaic puzzle application on nomophobia in adolescents. The data for the study will be collected over a 5-week period. The experimental group children will be asked to play mosaic puzzle games for 1 hour, 2 days a week for 5 weeks at a time deemed appropriate by the school under the supervision of the researcher. The control group children will not be given any application; they will only be observed, and a final test will be administered at the end of the 5 weeks. The study is planned as a single-center study, and a total of 30 children aged 12-14 with a nomophobia scale score of 60 or higher who meet the inclusion criteria will be included in the study.

No Intervention: Control Group

Arm Description: In the study, the child's level of nomophobia will first be determined using the Personal Information Form and the Nomophobia measurement tool in the control group. No intervention will be performed on the children in this group, and a test will be administered at the end of the intervention.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Mosaic Puzzle Intervention

This study aims to investigate the effect of mosaic puzzle application on nomophobia in adolescents. The data for the study will be collected over a 5-week period. The experimental group children will be asked to play mosaic puzzle games for 1 hour, 2 days a week for 5 weeks at a time deemed appropriate by the school under the supervision of the researcher. The control group children will not be given any application; they will only be observed, and a final test will be administered at the end of the 5 weeks. The study is planned as a single-center study, and a total of 30 children aged 12-14 with a nomophobia scale score of 60 or higher who meet the inclusion criteria will be included in the study.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Score at least 60 points on the nomophobia scale
* Be between the ages of 12 and 14
* Written consent from parents and verbal consent from the child

Exclusion Criteria

* Be under 12 years of age and over 14 years of age
* Have scored less than 60 points on the nomophobia scale
Minimum Eligible Age

12 Years

Maximum Eligible Age

14 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Pamukkale University scientific research project department

UNKNOWN

Sponsor Role collaborator

Rabia Nur TEKİ KESKİN

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Rabia Nur TEKİ KESKİN

Nurse (PhD Candidate)

Responsibility Role SPONSOR_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Pamukkale University

Denizli, Kınıklı, Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

PamukkaleU-SBE-RNTK-01

Identifier Type: -

Identifier Source: org_study_id