Virtual Rehabilitation Assistant Via Instant Messaging Communication to Promote Adherence to Rehabilitation After Reverse Shoulder Replacement
NCT ID: NCT06153381
Last Updated: 2023-12-12
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.
RECRUITING
NA
30 participants
INTERVENTIONAL
2023-09-01
2024-06-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Chatbot care
Chatbot
Rehabilitation program based on standard care, but assisted via an instant messaging application using a personal smartphone
Standard car
Rehabilitation program based on standard care, assisted with one education session plus informative brochure
Standard care
Standard car
Rehabilitation program based on standard care, assisted with one education session plus informative brochure
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Chatbot
Rehabilitation program based on standard care, but assisted via an instant messaging application using a personal smartphone
Standard car
Rehabilitation program based on standard care, assisted with one education session plus informative brochure
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* With a personal smartphone
* An instant messaging application installed
* Familiar with the use of such an application (i.e., at least three accessess per week)
* Able to write and read in the Spanish language
Exclusion Criteria
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hospital Universitario La Fe
OTHER
University of Valencia
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Jose MarÃa Blasco Igual
Principal Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hospital Universitario y Politécnico La Fe
Valencia, Valencia, Spain
Countries
Review the countries where the study has at least one active or historical site.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Marta Navarro, MD
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
SIP_LaFe
Identifier Type: -
Identifier Source: org_study_id