The Turkish Version of the Parental Smartphone Use Management Scale (PSUMS)

Sponsor
Istanbul University-Cerrahpasa (Other)
Overall Status
Completed
CT.gov ID
NCT04409106
Collaborator
(none)
200
1
5
39.8

Study Details

Study Description

Brief Summary

Parental Smartphone Use Management Scale (PSUMS) was originally developed in English language to parents to educate adolescents and communicate with them about online behavior and safety, as well as to conduct plans to manage adolescents' internet and smartphone use. The purpose of this study was to translate and cross-culturally adapt the PSUMS.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Parental Smartphone Use Management Scale (PSUMS) was originally developed in English language to parents to educate adolescents and communicate with them about online behavior and safety, as well as to conduct plans to manage adolescents' internet and smartphone use. The purpose of this study was to translate and cross-culturally adapt the PSUMS. The study will include adults who have been using smartphones for at least the past month and have children aged 11-18. For cross-cultural adaptation, two bi-lingual translators used the back-translation procedure. Within a 5-to-7 day period after first assessment, the participants completed the Turkish version of the Parental Smartphone Use Management Scale (PSUMS) to evaluate test-retest reliability. Cronbach's alpha (α) was used to assess internal consistency. The correlations with the Turkish version of The Smart Phone Addiction Scale-Short Form for Adolescent and the Turkish version of PedsQL in Adolescents 13-18 years old will determine to check the validity.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    200 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Cross-Sectional
    Official Title:
    The Reliability and Validity of the Turkish Version of the Parental Smartphone Use Management Scale (PSUMS)
    Actual Study Start Date :
    Sep 10, 2020
    Actual Primary Completion Date :
    Oct 1, 2020
    Actual Study Completion Date :
    Feb 10, 2021

    Outcome Measures

    Primary Outcome Measures

    1. Parental Smartphone Use Management Scale (PSUMS) [Baseline (First assessment)]

      Prior to developing the PSUMS, an item pool was established by conducting a literature review and a focus group. The item pool contained 18 items. A 7-point Likert scale was used to rate the level of agreement with items, ranging from 0 (no efficacy at all) to 6 (very strong efficacy).

    Secondary Outcome Measures

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

      Prior to developing the PSUMS, an item pool was established by conducting a literature review and a focus group. The item pool contained 18 items. A 7-point Likert scale was used to rate the level of agreement with items, ranging from 0 (no efficacy at all) to 6 (very strong efficacy).

    2. Smartphone Addiction Scale -Short form for adolescent Version (SAS-SF) [Baseline (First assessment)]

      Smartphone Addiction Scale -Short form for adolescent Version (SAS-SF) is a self-report scale with 10 items rated on a 6-point Likert scale (1= largely untrue, 6= largely true). Higher scores from the scale indicate higher level of the smartphone addiction. . The validity and reliability study of the questionnaire was done in Turkish.

    3. PedsQL in Adolescents [Baseline (First assessment)]

      It is a general quality of life scale that evaluates the physical and psychosocial lives of children between the ages of 11-18. The scale prepared for the 13-18 age group has a parent and child form. The parent form is filled out by the caregiver and the adolescent form by the child included in the study separately and simultaneously. The most important features are that "PedsQL in adolescents" is short, it can be filled in about 5-10 minutes, and it is easy to apply and score by the researcher.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Working at Istanbul University-Cerrahpaşa Faculty of Health Sciences

    • Having children using smart phones for at least the last one month

    • Having children between aged 11 and 18 years.

    • Being a volunteer to participate

    Exclusion Criteria:
    • Having any serious vision problems or 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 Turkey

    Sponsors and Collaborators

    • Istanbul University-Cerrahpasa

    Investigators

    • Principal Investigator: Ebru KAYA MUTLU, PhD, Istanbul University - Cerrahpaşa

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ebru Kaya Mutlu, PT, PT, PhD, Assoc Prof., Istanbul University-Cerrahpasa
    ClinicalTrials.gov Identifier:
    NCT04409106
    Other Study ID Numbers:
    • 2020/5
    First Posted:
    Jun 1, 2020
    Last Update Posted:
    Feb 12, 2021
    Last Verified:
    Feb 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Ebru Kaya Mutlu, PT, PT, PhD, Assoc Prof., Istanbul University-Cerrahpasa
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 12, 2021