Relationships Between Nomophobia Levels and Perceived Stress, Body Image and Food Addiction Among University Students

April 15, 2026 updated by: Beyza Terzioğlu, Bahçeşehir University

An Investigation of the Relationships Between Nomophobia Levels and Stress, Body Image and Food Addiction Among University Students

The purpose of this study is to examine the effects of nomophobia levels on stress, food addiction, and body image among undergraduate students aged 18-30 at Bahçeşehir University, Faculty of Health Sciences. The primary questions it aims to answer are:

  • Is there a statistically significant relationship between nomophobia levels and perceived stress, food addiction, and body image among university students?
  • Is there a correlation between objective anthropometric data (body fat percentage, skeletal muscle mass) measured via Bioelectrical Impedance Analysis (BIA), waist/hip circumference measurements, and the individual's perceived body image?

Study Overview

Detailed Description

The data collection process for this study will involve undergraduate students aged 18-30 at Bahçeşehir University, Faculty of Health Sciences. Participants will first complete a survey consisting of a socio-demographic form, daily screen time tracking, the Nomophobia Questionnaire (NMP-Q), the Perceived Stress Scale (PSS-10), the Yale Food Addiction Scale (YFAS), and the Stunkard Figure Rating Scale (FRS) to assess subjective body image.To ensure the accuracy of the biological data, participants will be required to follow a standardized measurement protocol, including at least 8 hours of fasting, avoidance of heavy physical activity prior to the assessment, and the removal of all metal accessories. Under these conditions, objective physical data will be gathered using the InBody 270 body composition analyzer via Bioelectrical Impedance Analysis (BIA) to record body weight (kg), body fat percentage (%), and skeletal muscle mass (kg). Additionally, anthropometric measurements including waist and hip circumferences (cm) will be manually collected using a standardized non-elastic tape to calculate Body Mass Index (BMI) and Waist-to-Hip Ratio (WHR). These objective metrics will be compared with the participants' subjective survey responses to analyze the impact of nomophobia on body image distortion, stress levels, and eating behaviors.

Study Type

Observational

Enrollment (Estimated)

150

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • beşiktaş
      • Istanbul, beşiktaş, Turkey (Türkiye), 34353
        • Recruiting
        • Bahçeşehir University, Faculty of Health Sciences
        • Contact:
        • Contact:

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

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

The study population consists of university students who are active smartphone users and have provided informed consent. Participants do not have pacemakers, metallic prostheses, or pregnancy, and they do not have diagnosed metabolic disorders (e.g., Cushing's syndrome, diabetes, thyroid disorders) or psychiatric conditions that could affect eating behavior. Individuals with current eating disorders, severe psychiatric diagnoses, regular use of psychiatric medications, recent corticosteroid or hormone therapy, or those who do not complete the questionnaires and measurement procedures are excluded.

Description

Inclusion Criteria:

  • Being an active smartphone user
  • Reading and providing consent via the Informed Consent Form
  • Absence of conditions such as pacemaker implantation, metallic prostheses in the body, or pregnancy
  • Not having a diagnosed metabolic disorder (e.g., Cushing's syndrome, diabetes, thyroid disorders) or any acute/chronic psychiatric condition that may affect eating behavior

Exclusion Criteria:

  • Individuals with a current diagnosis of an eating disorder (e.g., anorexia nervosa, bulimia nervosa, binge eating disorder, etc.)
  • Individuals with a psychiatric diagnosis of severe depression, bipolar disorder, psychotic disorder, or an anxiety disorder requiring treatment
  • Individuals who regularly use psychiatric medications (e.g., SSRIs, SNRIs, antipsychotics, mood stabilizers, etc.)
  • Individuals who have used corticosteroids or similar hormone-regulating medications in the past 3 months
  • Pregnant or breastfeeding individuals
  • Participants who did not complete the questionnaires or the measurement procedures

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
University Students
Participants (n:150) will complete questionnaires assessing nomophobia, perceived stress, body image, and food addiction. In addition, objective anthropometric measurements, including body composition (fat mass, muscle mass) via Bioelectrical Impedance Analysis (InBody 270) and waist-to-hip ratio measurements, will be collected. No drugs or treatments are administered.
Participants will complete self-report questionnaires including the Nomophobia Questionnaire (NMP-Q), Perceived Stress Scale (PSS-10), Body Image Questionnaire (BIQ), Food Addiction Scale (YFAS 2.0), and the Stunkard Figure Rating Scale (FRS). Objective anthropometric measurements, including body composition using InBody 270 and waist-to-hip ratio, will also be obtained.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Nomophobia
Time Frame: Baseline

The level of nomophobia experienced by participants, measured using the Nomophobia Questionnaire (NMP-Q).

This form aims to assess your feelings and thoughts when you cannot access your smartphone or are away from it, a condition known as nomophobia. There are no right or wrong answers; what matters is answering honestly based on your own experience. Indicate your level of agreement with each statement about your smartphone use (1 = strongly agree, 7 = strongly disagree).

Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perceived Stress
Time Frame: Baseline

The level of stress perceived by participants, measured using the Perceived Stress Scale (PSS).

Below are a series of questions about your personal experiences over the past month. Please read each question carefully and mark the box under the option that best reflects you. There are no right or wrong answers; what matters is that you respond in a way that reflects your own feelings and thoughts.

Never - Almost Never - Sometimes - Quite Often - Very Often

Baseline
Body Image
Time Frame: Baseline

Self-perceived body image assessed using the Stunkard Figure Rating Scale (FRS), where participants select a figure that best represents their current and ideal body shape.

The images in this section are designed to assess individuals' body perception. Below are figures representing different body types. Please examine these figures carefully and select the one that you think best represents you at the moment. There are no right or wrong answers in this study; what matters is reflecting your own perception as accurately as possible.

Baseline
Food Addiction
Time Frame: Baseline

Assessment of addictive eating behaviors using the Yale Food Addiction Scale 2.0 (YFAS 2.0).

This questionnaire asks about your eating habits over the past year. People sometimes have difficulty controlling their intake of certain foods, such as;

  • Sweets like ice cream, chocolate, pastries, cookies, cake, and candy
  • Starches such as white bread, bread, pasta, and rice
  • Salty snacks like chips, pretzels, and crackers
  • Fatty foods such as steak, bacon, hamburgers, cheeseburgers, pizza, and French fries
  • Sugary drinks like soda and fruit juice

When the following questions refer to SPECIFIC FOODS, please think of ANY foods similar to those listed in each category, or ANY OTHER foods that you may have had problems with during the past year.

Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Beyza Terzioğlu, Bahcesehir university
  • Study Chair: Ecenur Özkul Erdoğan, PhD, Bahcesehir university

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)

February 10, 2026

Primary Completion (Actual)

April 1, 2026

Study Completion (Estimated)

May 1, 2026

Study Registration Dates

First Submitted

April 2, 2026

First Submitted That Met QC Criteria

April 2, 2026

First Posted (Actual)

April 8, 2026

Study Record Updates

Last Update Posted (Actual)

April 17, 2026

Last Update Submitted That Met QC Criteria

April 15, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

No individual participant data (IPD) will be shared with other researchers. Individual-level data will remain confidential in accordance with data protection regulations (e.g., KVKK); however, aggregated data, summary statistics, and group-level results may be reported in publications and presentations.

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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