- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06006364
Investigation of the Effect of Nomophobia on Musculoskeletal System and Sleep
Study Overview
Detailed Description
The research was planned as a quantitative research. Data collection was done online.
The scales and forms used are as follows:
- Demographic Information Form
- Nomophobia Scale
- Cornell Musculoskeletal Disorder Questionnaire
- Smart phone Addiction Scale
- Pittsburgh Sleep Quality Index
- International Physical Activity Survey
- McGill Melzack Pain Questionnaire
Questionnaires will be sent to the participants online by invitation. Participants will be asked to participate in the study by reaching them through social media, mail or mobile phone applications. The data obtained will be analyzed statistically.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Contact
- Name: Ömer ŞEVGİN
- Phone Number: +90506 978 75 35
- Email: omer.sevgin@uskudar.edu.tr
Study Locations
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-
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Istanbul, Turkey
- Uskudar University
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Contact:
- Ömer ŞEVGİN
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- To have accepted the voluntary consent form that requires participation in the survey study.
- Being a smart phone user
Exclusion Criteria:
- Not accepting the volunteer consent form
- Having undergone previous surgery
- Being on antidepressants.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
1.Group
Nomophobia Level:none
|
The scales and forms used are respectively:
|
2.Group
Nomophobia Level: mild
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The scales and forms used are respectively:
|
3.Group
Nomophobia Level: medium
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The scales and forms used are respectively:
|
4.Group
Nomophobia Level: extreme
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The scales and forms used are respectively:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Nomophobia Scale
Time Frame: 2 days
|
The Nomophobia Scale was itemized according to a 7-point Likert type.
Out of 20 items in total consists of.
The scale has four sub-dimensions: Lack of Access to Information (4 items), Losing Connection (5 items), Inability to Communicate (6 items), and Comfort Inability to feel (5 items).
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2 days
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Cornell Musculoskeletal Disorder Questionnaire
Time Frame: 2 days
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The questionnaire was conducted in 11 body regions (neck, right and left shoulder, upper arm, forearm and wrist, back and waist region) includes questions about the frequency of musculoskeletal disorders (pain/pain/discomfort), the severity of these disorders, and whether they interfere with work.
|
2 days
|
Smart phone Addiction Scale
Time Frame: 2 days
|
It is a scale developed to measure the risk of smart phone addiction, consisting of 10 items and evaluated with a six-point Likert scale.
Scale items were scored from 1 to 6. Scale scores range from 10 to 60.
As the score obtained from the test increases, it is considered that the risk for addiction increases.
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2 days
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Pittsburgh Sleep Quality Index
Time Frame: 2 days
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It is a 19-item self-report scale that evaluates sleep quality and impairment over the past month.
It consists of 24 questions, 19 questions are self-report questions, 5 questions are questions to be answered by the spouse or roommate.
The 18 scored questions of the scale consist of 7 components.
Subjective Sleep Quality, Sleep Latency, Sleep Duration, Habitual Sleep Efficiency, Sleep Disorder, Sleeping Drug Use and Daytime Dysfunction.
Each component is evaluated over 0-3 points.
The total score of the 7 components gives the scale total score.
The total score ranges from 0 to 21.
A total score greater than 5 indicates "poor sleep quality".
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2 days
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International Physical Activity Questionnaire Short Form
Time Frame: 2 days
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The questionnaire consisting of seven questions including the activities of the last seven days was prepared by the individuals themselves. self-applicable and provides information about the time people spend in moderate to vigorous activities |
2 days
|
McGill Melzack Pain Questionnaire
Time Frame: 2 days
|
Pain Questionnaire consists of four parts.
With the McGill Melzack Pain Questionnaire, the location of the pain, the feeling it creates in the individual, its relationship with time, its severity and the level of livable pain for the individual are determined.
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2 days
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Melek ÖZCAN, Uskudar University
Publications and helpful links
General Publications
- Bhattacharya S, Bashar MA, Srivastava A, Singh A. NOMOPHOBIA: NO MObile PHone PhoBIA. J Family Med Prim Care. 2019 Apr;8(4):1297-1300. doi: 10.4103/jfmpc.jfmpc_71_19.
- Kuscu TD, Gumustas F, Rodopman Arman A, Goksu M. The relationship between nomophobia and psychiatric symptoms in adolescents. Int J Psychiatry Clin Pract. 2021 Mar;25(1):56-61. doi: 10.1080/13651501.2020.1819334. Epub 2020 Sep 17.
- Notara V, Vagka E, Gnardellis C, Lagiou A. The Emerging Phenomenon of Nomophobia in Young Adults: A Systematic Review Study. Addict Health. 2021 Apr;13(2):120-136. doi: 10.22122/ahj.v13i2.309.
- Rahme C, Hallit R, Akel M, Chalhoub C, Hachem M, Hallit S, Obeid S. Nomophobia and temperaments in Lebanon: Results of a national study. Perspect Psychiatr Care. 2022 Oct;58(4):1607-1612. doi: 10.1111/ppc.12968. Epub 2021 Nov 6.
- Jahrami HA, Fekih-Romdhane F, Saif ZQ, Alhaj OA, AlRasheed MM, Pandi-Perumal SR, BaHammam AS, Vitiello MV. Sleep dissatisfaction is a potential marker for nomophobia in adults. Sleep Med. 2022 Oct;98:152-157. doi: 10.1016/j.sleep.2022.07.001. Epub 2022 Jul 11.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Uskudar55
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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