NCT07097610

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 15, 2025

Completed
28 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 15, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 25, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

July 23, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 31, 2025

Completed
Last Updated

July 31, 2025

Status Verified

July 1, 2025

Enrollment Period

28 days

First QC Date

July 23, 2025

Last Update Submit

July 30, 2025

Conditions

Keywords

nomophobiachilddependencesmart phone addictionpuzzle activity

Outcome Measures

Primary Outcomes (1)

  • Nomophobia Scale (NO) for the 9-18 Age Group

    The Nomophobia Scale developed by Yıldırım and Correia (2015) is a Likert-type measure that assesses the level of fear experienced by children when they do not have access to their cell phones. The validity and reliability of the scale were studied by Özdemir and Bektaş (2020). The scale consists of 20 items. It is a 7-point Likert-type scale (1: Strongly disagree; 7: Strongly agree). The scale has four subscales: inability to access information, giving up comfort, inability to communicate, and loss of online connection. A score of 20 on the scale indicates no nomophobia, 21 ≤ NÖ Score \< 60 indicates mild nomophobia, 60 ≤ NÖ Score \< 100 indicates moderate nomophobia, and 100 ≤ NÖ Score ≤ 140 indicates severe nomophobia. The scale ranges from a minimum of 20 to a maximum of 140 points. As the score increases, the level of nomophobia increases. Individuals who score 61 or higher on the raw score can be classified as having 'severe or moderate' nomophobia.

    From enrollment to the end of treatment at 10 weeks.

Study Arms (2)

Experimental: "Mosaic Puzzle Intervention Group"

EXPERIMENTAL

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

Other: Mosaic Puzzle Intervention

No Intervention: Control Group

NO INTERVENTION

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.

Interventions

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.

Experimental: "Mosaic Puzzle Intervention Group"

Eligibility Criteria

Age12 Years - 14 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • 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

You may not qualify if:

  • Be under 12 years of age and over 14 years of age
  • Have scored less than 60 points on the nomophobia scale

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Pamukkale University

Denizli, Kınıklı, 20160, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: The study includes one intervention group and one control group.
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Nurse (PhD Candidate)

Study Record Dates

First Submitted

July 23, 2025

First Posted

July 31, 2025

Study Start

February 15, 2025

Primary Completion

March 15, 2025

Study Completion

May 25, 2025

Last Updated

July 31, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations