Available Assistive Technology Outcome Measures: Systematic Review.
Francesca Borgnis, Lorenzo Desideri, Rosa Maria Converti...
https://pubmed.ncbi.nlm.nih.gov/37782310Actively Recruiting
Led by Fondazione Don Carlo Gnocchi Onlus · Updated on 2025-08-26
50
Participants Needed
1
Research Sites
4 weeks
Total Duration
F
Fondazione Don Carlo Gnocchi Onlus
Lead Sponsor
M
Ministry of Health, Italy
Collaborating Sponsor
This research aims to improve the quality of prosthetic interventions and assess the suitability of assistive devices used for Augmentative Alternative Communication (AAC), computer accessibility, and environmental control. The study will recruit fifty patients who require these prosthetic interventions, including devices such as communicators, specialized keyboards, mouse emulators, eye pointers, accessibility software, and remote controls. The study is observational and conducted at the Fondazione Don Carlo Gnocchi "IRCCS S.Maria Nascente" in Milan. At the start (T0), patients will undergo clinical and cognitive evaluations by a physician and psychologist using various assessment tools administered via accessible software on PCs or web pages. Based on these assessments, the most appropriate assistive solution will be prescribed or suggested. The assistive devices will be classified according to international standards. Participants will then be followed up 3 to 6 months after receiving their assistive technology (T1), during which the assessments will be repeated to measure outcomes. Throughout the study, participants will complete questionnaires and tests including quality of life measures, satisfaction with assistive technology, and the importance and severity of problems they expect to improve. Data will be collected at baseline and follow-up to evaluate the effectiveness and satisfaction with the assistive devices. The study aims to use both quantitative and qualitative data to understand the outcomes of these interventions over the course of 3 to 6 months.
CONDITIONS
Outcomes of ICT Assistive Technology in RehabiliTAtIoN Pathways
You may qualify if you...
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - At baseline
Participants undergo clinical and cognitive assessments to evaluate their needs for assistive technology. The multidisciplinary team identifies and prescribes the most appropriate assistive solution based on these assessments.
1 visit (in-person)
Duration - 3 to 6 months after receiving assistive solution
Participants are contacted 3 to 6 months after receiving the assistive solution to assess satisfaction and outcomes using questionnaires and scales.
1 follow-up visit (in-person)
Total: 1 location
1
IRCCS Fondazione Don Carlo Gnocchi ONLUS
Milan, MI, Italy, 20148
Actively Recruiting
C
Claudia Salatino
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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