Herramienta De Procesamiento De Lenguaje Natural En Dispositivo Móvil Inteligente Para Fomentar La Adherencia a La Rehabilitación Domiciliaria
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- University of Valencia
- Enrollment
- 65
- Locations
- 1
- Primary Endpoint
- Adherence
Study Overview
Brief Summary
A Chatbot oriented to virtually assist patients in a physiotherapy treatment has been designed and developed to interact with patients with musculoskeletal disorders in need for domiciliary rehabilitation. The tool has been designed to promote adherence to rehabilitation, what in turn may have an impact on clinical outcome. A randomized clinical trial involving patients undergoing total knee replacement has bee designed to determine the applicability of the proposal. The participants will be assigned into exerimental group (intervention with the software tool) or control group (standard care).
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Double (Participant, Outcomes Assessor)
Eligibility Criteria
- Ages
- — to 75 Years (Child, Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Individuals on the waiting list for total knee replacement surgery
- •Undergoing primary total knee replacement surgery
- •Who have a personal smartphone
- •Who have an instant messaging application installed
- •Familiar with the use of such application (more than 3 accesses per week),
Exclusion Criteria
- •Evident cognitive state that prevents to understand care provider instructions
- •Vestibular or central nervous system affection (e.g. stroke)
- •Cannot read or write
- •Do not understand Spanish language
- •Not able to consent to participate
Arms & Interventions
Control
Intervention: Standard care (Other)
Experimental
Intervention: Chatbot Assistant (Other)
Outcomes
Primary Outcomes
Adherence
Time Frame: Change from baseline to 3 months after surgery date
Compliance with intervention measured as the percentage of sessions carried out with respect to the total planned
Secondary Outcomes
- Knee Pain(Change from baseline to 3 months and one year after surgery date)
- Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)(Change from baseline to 3 months and one year after surgery date)
Investigators
Jose María Blasco Igual
Principal investigator
University of Valencia