The Effect of Self-Compassion Practices on Nomophobia Symptoms in Young Adults

July 7, 2025 updated by: Behice Belkıs ÇALIŞKAN, University of Beykent

The Effect of Self-Compassion Practices on Nomophobia Symptoms in Young Adults; A Randomized Controlled Trial

The term nomophobia, which can also be defined as a symptom, has emerged with the excessive use of smartphones. Nomophobia is the anxiety and fear that people feel when they are away from their phones for any reason. Nomophobia is defined as the "fear of being deprived of phone or internet access." According to DSM5, "situational phobias are excessive, irrational fears accompanied by anxiety and distress towards a specific object or situation." Considering the anxiety, stress, and worry it creates on individuals, Bragazzi and Del Puente (2014) stated that nomophobia should be added to the DSM-5 due to the dimensions of the anxiety, stress, and worry it creates on individuals and the speed at which it spreads. They explained the symptoms of nomophobia as follows; spending most of the day with a smartphone, constantly checking the battery, in case of being away from the smartphone, thoughts such as the battery or credit running out and not being able to find the phone create anxiety in individuals, staying away from places and spaces where it is not possible to use a smartphone, constantly checking whether notifications or messages have arrived, keeping the smartphone on and nearby even while sleeping, communicating using digital tools because face-to-face conversation creates anxiety, incurring extraordinary expenses for a smartphone or getting into excessive debt.

In addition to making life easier, nomophobia, which occurs with excessive and uncontrolled use of smartphones, can cause some problems. Increasing individuality and the resulting weakening of face-to-face communication bring about addictive applications, depression, headache, visual impairments, sleep problems, musculoskeletal problems, and physiological and psychological problems.

To cope with and manage the symptoms of an addictive condition such as nomophobia, it is envisaged that young adults should be supported with self-compassion practices.

Self-compassion exists from the essence of awareness when we encounter painful and distressing situations. Self-compassion tells individuals to be kind to themselves when they encounter pain and distress. When people encounter an adverse life event, they blame themselves, criticize themselves, react to themselves, and make harmful decisions. A happy and peaceful life emerges thanks to self-compassion, a sense of security, and health. If individuals can accept and tolerate many positive and negative life events and be kind and tolerant towards themselves, they can stop limiting and ignoring their feelings and thoughts. In this way, they can avoid over-identifying by realizing that the experiences experienced are experiences that many people can experience. Individuals with high levels of self-compassion have low levels of depression, anxiety, stress, perfectionism, rumination, and suppressing thoughts. In addition, since they do not judge themselves, their happiness, optimism, enjoyment of life, and motivation are high. In line with this information, self-compassion practices can be supportive during this period when young adults encounter a problem such as nomophobia and have to manage many physiological symptoms. This study aimed to determine the effect of self-compassion practices on nomophobia symptoms in young adults.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

120

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 Contact

Study Locations

      • Istanbul, Turkey
        • Beykent ün

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

Yes

Description

Inclusion Criteria:

  • Volunteering to participate in the study
  • Being between the ages of 18-30
  • Not having any psychiatric problems

Exclusion Criteria:

  • Being under 18 years of age

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: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimantal group
This group will be given an online self-compassion program for 8 weeks..
Program includes four basic practices: breathing meditation, walking meditation, body scan, and mindful movement. Consciously focusing on what is happening allows people to observe and accept what they are experiencing in their bodies, minds, and the world around them at that moment. Mindfulness practices are an 8-week practice consisting of 2-2.5 hour sessions per week by a trained instructor, mindfulness meditation practices, yoga practices, examining the psychological and physiological aspects of stress, and recently including the concept of self-compassion. In addition, daily practices are given to participants, and a suitable day is determined as a retreat day. The aim is to enable individuals to reveal and experience their thoughts, emotions, and bodily sensations and to increase emotional tolerance by revealing avoidance behaviors. Individuals learn to return to and accept intense bodily sensations and emotional discomfort with mindfulness.
No Intervention: Control Group
There will be no intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Nomophobia Scale
Time Frame: To be filled after the 8-week training program is completed
File Nomophobia Scale by Yıldırım and Correia (2015) consists of 20 items. The scale is answered from 1 (Strongly Disagree) to 7 (Strongly Agree). The scale is a 7-point Likert type. It consists of 4 sub-dimensions: "Inability to Access Information" (4 items), "Sacrificing Comfort" (5 items), "Inability to Communicate" (6 items) and "Losing Online Connection" (5 items) (Yıldırım and Correia, 2015). Participants are between 20 and 140 on the Nomophobia Scale. It is seen that participants with less than 20 points do not have nomophobia and those with 100-14 points have extreme nomophobia. The original systems of the scale were calculated as .95. The reliability in this study was based on Cronbach's alpha value of .95.
To be filled after the 8-week training program is completed

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-Compassion Scale Short Form (SCF-K)
Time Frame: To be filled after the 8-week training program is completed
Self-Compassion Scale Short Form (SCF-K); The scale developed by Raes, Pommier, Neff, and Van Gucht (2011) considering it to be more convenient than the long form in terms of time was used. SCF-K, consisting of items taken from the 26-item Self-Compassion Scale, included two items for each subcomponent of self-compassion in order to create this short form, and there are 12 items in total. It is seen that the scale has started to be used in Western literature in recent years, especially due to its ease of use. The Turkish adaptation of the Self-Compassion Scale Short Form was made by Yıldırım and Sarı (2018).
To be filled after the 8-week training program is completed

Collaborators and Investigators

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

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 (Estimated)

August 25, 2025

Primary Completion (Estimated)

October 28, 2025

Study Completion (Estimated)

March 25, 2026

Study Registration Dates

First Submitted

July 7, 2025

First Submitted That Met QC Criteria

July 7, 2025

First Posted (Actual)

July 16, 2025

Study Record Updates

Last Update Posted (Actual)

July 16, 2025

Last Update Submitted That Met QC Criteria

July 7, 2025

Last Verified

July 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • E-45778635-050.99-182837

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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