Validation of the French ATI Scale and Predisposition to Use Technological Tools in Rehabilitation.

NCT06363279 | Recruiting

• 1 other identifier: 2024/24JAN/044
• Study Type: interventional
• Target: 1,000
• Locations: 1 country
• Sites: 1

Brief Summary

Aim of the study: The first aim of this study is to validate the translation of the Affinity for Technology Interaction (ATI) questionnaire. This questionnaire was developed in English by Franke, Attig and Wessel in 2019. It consists of 9 items and was developed to assess a person's tendency to actively engage in technological interaction, or the ease with which a person uses technological tools. Currently, the questionnaire has been translated into French by our research team according to good practice recommendations, but this French version has not yet been validated. To validate the translation of a questionnaire, it is necessary to have it completed by a large number of subjects from the population of interest. In neurorehabilitation, measuring this affinity will make it possible to better identify patients who are more likely to adhere to tele-rehabilitation and thus direct them towards this type of treatment as a complement to conventional rehabilitation. The second objective is to determine the extent to which the general population is prepared to use technological tools as part of their rehabilitation. The aim is to gain a better understanding of the profile of people who could potentially benefit from tele-rehabilitation. Accessibility to the technologies, their expectations and barriers will also be explored as part of this study.

Conditions

Stroke

Outcome Measures

Primary Outcomes (1)

• ATI - affinity technology interaction scale

  Evaluation scale in the form of a self-questionnaire to assess a person's affinity with technological communication tools. French version of the ATI questionnaire: Questionnaire consisting of 9 items designed to assess the affinity for interaction with technological systems (such as mobile phones, computers, television, etc.). The response options for each item are in the form of a Likert scale ranging from "strongly disagree" (= 1) to "strongly agree" (= 6). A total score including the 9 items is then calculated to obtain the subject's score.

  Baseline

Secondary Outcomes (1)

• Scale for assessing a person's readiness to use technological tools as part of their rehabilitation

  Basline

Study Arms (1)

Questionnaires on predisposition to the use of technology

OTHER

The questionnaire is divided into 4 main sections: * General information: Questions on age, gender, postal code, country, socio-professional status and level of education. * ATI questionnaire in French: Questionnaire consisting of 9 items to assess affinity for interaction with technological systems (such as mobile phones, computers, television, etc.). * Face validity and perceived usefulness: Five statements designed to assess the face validity and perceived usefulness of the questionnaire to respondents. The response options for each statement are in the form of a Likert scale ranging from 'strongly disagree' to 'strongly agree'. * Predisposition to use technology: Questionnaire to assess predisposition to use new technologies in general and specifically in telerehabilitation.

Other: Conducting questionnaires

Interventions

Conducting questionnaires OTHER

The questionnaires will be administered online or in person.

Questionnaires on predisposition to the use of technology

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Adult subjects (\> 18 years)
• Speak and understand French;
• Be able to give consent in paper or electronic format.
• Have had a single stroke;
• Have been out of hospital for at least 1 month.

You may not qualify if:

• Severe comprehension problems ;
• Inability to complete the questionnaire;
• Severe comprehension problems, prior to or following the stroke, preventing planned assessments.

Sponsors & Collaborators

• Cliniques universitaires Saint-Luc- Université Catholique de Louvain: lead

Study Sites (1)

Clinique Universitaires Saint-Luc

Brussels, Woluwé-Saint-Lambert, 1200, Belgium

RECRUITING

MeSH Terms

Conditions

Stroke

Condition Hierarchy (Ancestors)

Cerebrovascular Disorders; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Vascular Diseases; Cardiovascular Diseases

Study Officials

• Lejeune Thierry

  Cliniques universitaires Saint-Luc- Université Catholique de Louvain

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Lejeune Thierry

CONTACT

027641648; thierry.lejeune@saintluc.uclouvain.be

Van Durme Mathilde

CONTACT

0473423735; mathilde.vandurme@saintluc.uclouvain.be

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: OTHER
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 9, 2024
• First Posted: April 12, 2024
• Study Start: April 4, 2024
• Primary Completion: September 1, 2024
• Study Completion: October 1, 2024
• Last Updated: May 2, 2024

Record last verified: 2024-04

Locations

BE (1)