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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04337775
Other study ID # 3278
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 7, 2020
Est. completion date July 27, 2020

Study information

Verified date July 2020
Source Istanbul University-Cerrahpasa
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 264
Est. completion date July 27, 2020
Est. primary completion date June 8, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility 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

Study Design


Locations

Country Name City State
Turkey Istanbul University-Cerrahpasa Istanbul Bakirkoy

Sponsors (1)

Lead Sponsor Collaborator
Istanbul University-Cerrahpasa

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Smartphone Impact Scale 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. Baseline (First assessment)
Secondary Smartphone Impact Scale 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. Within a 5-to-7-day period after the first assessment (Second assessment)
Secondary Smartphone Addiction Scale 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. Baseline (First assessment)
Secondary Nottingham Health Profile 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. Baseline (First assessment)
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