Turkish Version of the Smart Tools Proneness Questionnaire
NCT ID: NCT06148987
Last Updated: 2024-02-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
330 participants
OBSERVATIONAL
2023-12-15
2024-02-06
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Based on these collective theories, the Smart Tools Proneness Questionnaire (STP-Q), developed by Navarro J. and colleagues, aims to explore and measure interindividual differences influencing an individual's propensity to use smart tools, their initial selection of smart tools, and subsequent usage. In practice, measuring the propensity of any individual to use smart tools will be significantly beneficial for both professionals and non-professionals involved in designing, producing, and implementing such tools. Therefore, the purpose of this study is to translate, validate, and establish the reliability of the Turkish version of the STP-Q.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Validity and Reliability of the Turkish Version of the Testing Emotionalism After Recent Stroke - Questionnaire
NCT05822986
Turkish Adaptation of Heart Health Self-efficacy and Self-Management Scale
NCT05939297
Turkish Validity and Reliability of the Social Frailty Index
NCT06288789
Turkish Version of Computer Usage Proficiency Questionnaire
NCT06794463
Reliability and Validity of the Turkish Version of the Laval
NCT06243055
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Smart tools are understood as any machine or device that can complete tasks involving information, mechanics, or electronics in lieu of or in connection with individuals. The smartphone can now be considered a ubiquitous example of such tools, reaching approximately half or more of the global population in the past decade. In high-income countries in North America and Europe, over 80% of the population owns a smartphone. The idea that individual differences play a crucial role in the implementation of any technological innovation has become a recurring theme in various disciplines, including information systems, manufacturing, and marketing.
Technologically advanced tool solutions (i.e., the highest level of automation) may not always be the preferred choice for participants when given an option. Various experiments show that in vehicles, low to moderate levels of automation are often preferred over highly automated vehicles. The association of higher task demands with smarter tools has been reported to influence tool selection along with task demand. However, participants may avoid using a fully automatic tool even if the task is highly laborious. In fact, in a series of experiments, participants more distinctly preferred manually completing routine tasks over more efficient fully automatic task completion.
Based on these collective theories, the Smart Tools Proneness Questionnaire (STP-Q), developed by Navarro J. and colleagues, aims to explore and measure interindividual differences influencing an individual's propensity to use smart tools, their initial selection of smart tools, and subsequent usage. In practice, measuring the propensity of any individual to use smart tools will be significantly beneficial for both professionals and non-professionals involved in designing, producing, and implementing such tools. Therefore, the purpose of this study is to translate, validate, and establish the reliability of the Turkish version of the STP-Q.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
OTHER
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Questionnaire group
This study will be conducted in Turkey between January and August Ferbruary 2024, and it aims to investigate the Turkish translation, reliability, and validity of the AAE-A survey. All participants must meet the following inclusion criteria: (i) be 18 years old or older, (ii) use smart devices and tools, and (iii) provide written consent to participate. Participants with specific abnormalities such as cognitive or neurological disorders, upper extremity pain, functional limitations, or cognitive impairments will be excluded from the study to ensure the accuracy of the norms. It is estimated that a sample size of 270 individuals, with 10 individuals per item, will be needed for the sample size of this study."
Questionnaire
The translation and cultural adaptation of the survey will be conducted according to the guidelines of Beaton et al. Following the Beaton guidelines, the translation and cultural adaptation steps are as follows: 1) The original version of the survey will be translated into Turkish separately by two individuals whose native language is Turkish and who are proficient in English. One translator will be an English linguistics scholar unfamiliar with the concepts and terms, while the other will be a physiotherapist familiar with the concepts and terms; 2) Subsequently, the translations will be merged into a single text by these two translators; 3) The final Turkish version of the survey will be translated back into English by two translators who are unaware of the study; 4) The translations will then be combined by these two translators to create a harmonized and single text; 5) The back-translation and cultural adaptation
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Questionnaire
The translation and cultural adaptation of the survey will be conducted according to the guidelines of Beaton et al. Following the Beaton guidelines, the translation and cultural adaptation steps are as follows: 1) The original version of the survey will be translated into Turkish separately by two individuals whose native language is Turkish and who are proficient in English. One translator will be an English linguistics scholar unfamiliar with the concepts and terms, while the other will be a physiotherapist familiar with the concepts and terms; 2) Subsequently, the translations will be merged into a single text by these two translators; 3) The final Turkish version of the survey will be translated back into English by two translators who are unaware of the study; 4) The translations will then be combined by these two translators to create a harmonized and single text; 5) The back-translation and cultural adaptation
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* The inclusion criteria for participants in this validation study require individuals to be 18-55 years, actively use smart devices, provide written consent, possess proficiency in the Turkish language, and not have specific abnormalities or impairments that may hinder accurate survey completion. Ethical considerations, aligned with the principles of the Helsinki Declaration, will be maintained throughout the study.
Exclusion Criteria:
* Conversely, exclusion criteria involve disqualifying individuals below the age of 18 or above 55, non-users of smart devices, those unwilling to provide written consent, individuals lacking proficiency in Turkish, and those with physical or cognitive impairments. This comprehensive approach ensures that participants are suitable for the research, promoting reliable and meaningful responses while upholding ethical standards in the study's execution.
18 Years
55 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Çankırı Karatekin University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ceyhun Türkmen
Assoc. Prof.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Çankırı Karatekin University
Çankırı, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ab2e5654208645eb
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.