The Turkish Version of the Smartphone Impact Scale

Sponsor
Istanbul University-Cerrahpasa (Other)
Overall Status
Completed
CT.gov ID
NCT04337775
Collaborator
(none)
264
1
2.7
99.2

Study Details

Study Description

Brief Summary

Smartphone Impact Scale (SIS) was originally developed in English to determine the cognitive, affective, social, and behavioral impacts of smartphones in everyday life. The purpose of this study was to translate and cross-culturally adapt the SIS instrument into Turkish and investigate its psychometric properties.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Smartphone Impact Scale (SIS) was originally developed in English to determine the cognitive, affective, social, and behavioral impacts of smartphones in everyday life. The purpose of this study was to translate and cross-culturally adapt the SIS instrument into Turkish and investigate its psychometric properties. Two hundred healthy young adults will include. For cross-cultural adaptation, two bi-lingual translators used the back-translation procedure. Within a 5-to-7-day period after the first assessment, the participants completed the Turkish version of SIS (SIS-T) to evaluate test-retest reliability. Cronbach's alpha (α) was used to assess internal consistency. The correlations with the Turkish version of the Smartphone Addiction Scale (SAS-T) and Turkish version of the Nottingham Health Profile (NHP-T) will determine to check the validity.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    264 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Cross-Sectional
    Official Title:
    The Reliability and Validity of the Turkish Version of the Smartphone Impact Scale
    Actual Study Start Date :
    May 7, 2020
    Actual Primary Completion Date :
    Jun 8, 2020
    Actual Study Completion Date :
    Jul 27, 2020

    Outcome Measures

    Primary Outcome Measures

    1. Smartphone Impact Scale [Baseline (First assessment)]

      The Smartphone Impact Scale is a reliable and scale for evaluating cognitive, affective, social, and behavioral impacts of smartphones in everyday life. It assesses loss of control of smartphone use ,nomophobia, smartphone-mediated communication, emotion regulation through smartphone usage, smartphone support to romantic relationships, smartphone tasks support, and awareness of smartphone negative impact. A high score in the subscales shows a higher negative impact of smartphone on cognitive, affective, social, and behavioral aspects.

    Secondary Outcome Measures

    1. Smartphone Impact Scale [Within a 5-to-7-day period after the first assessment (Second assessment)]

      The Smartphone Impact Scale is a reliable and scale for evaluating cognitive, affective, social, and behavioral impacts of smartphones in everyday life. It assesses loss of control of smartphone use ,nomophobia, smartphone-mediated communication, emotion regulation through smartphone usage, smartphone support to romantic relationships, smartphone tasks support, and awareness of smartphone negative impact. A high score in the subscales shows a higher negative impact of smartphone on cognitive, affective, social, and behavioral aspects.

    2. Smartphone Addiction Scale [Baseline (First assessment)]

      Smartphone Addiction Scale (SAS) is a self-reported scale developed by Kwon et al. based on internet addiction and the features of smartphones in 20135. The scale consisted of 33 items rated on a 6-point Likert-type scale from 1 to 6. A high total score in the scale, which has no cut-off score, shows a smartphone addiction risk. The Turkish version of SAS (SAS-T), which was previously reported as a reliable instrument, will use in the present study.

    3. Nottingham Health Profile [Baseline (First assessment)]

      Nottingham Health Profile is patient-completed questionnaire used to determine and quantify perceived health problems. Composed of 38 items divided into six domains: 1) sleep, 2) mobility, 3) energy, 4) pain, 5) emotional reactions, 6) social isolation. Total Score ranges from 0 (no perceived distress) to 100 (maximum perceived distress). The Turkish version of Nottingham Health Profile, which was previously reported as a reliable and valid instrument, will use in the present study.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 35 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Aged between 18 and 35 years

    • Having a smartphone that was connected to the Internet for at least 6 months

    • Being a volunteer to participate

    Exclusion Criteria:
    • Having cognitive impairment

    • Having disabilities in understanding, speaking and reading Turkish

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Istanbul University-Cerrahpasa Istanbul Bakırkoy Turkey 34147

    Sponsors and Collaborators

    • Istanbul University-Cerrahpasa

    Investigators

    • Principal Investigator: Ebru Kaya Mutlu, PhD, Istanbul University-Cerrahpasa

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Tansu Birinci, PT, MSc Research Assistant, Istanbul University-Cerrahpasa
    ClinicalTrials.gov Identifier:
    NCT04337775
    Other Study ID Numbers:
    • 3278
    First Posted:
    Apr 8, 2020
    Last Update Posted:
    Jul 28, 2020
    Last Verified:
    Jul 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Tansu Birinci, PT, MSc Research Assistant, Istanbul University-Cerrahpasa
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 28, 2020