Integrating Artificial Intelligence Into International Classification of Functioning, Disability,… (NCT07021781) | Clinical Trial Compass
CompletedNot Applicable
Integrating Artificial Intelligence Into International Classification of Functioning, Disability, and Health Coding: Effectiveness of a Mobile Application for Patient Questionnaires
Kazakhstan185 participantsStarted 2024-11-25
Plain-language summary
Mobile applications and artificial intelligence are increasingly integrated into medical practice, yet their impact on workflow optimization and diagnostic accuracy remains understudied. This study evaluates the effectiveness of the MedQuest mobile application in optimizing patient questionnaire processes and assesses the accuracy of AI-driven International Classification of Functioning, Disability and Health (ICF) coding in comparison to traditional clinician-based coding.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Aged 18 and older.
. Owned a smartphone (iOS or Android operating system) with internet access.
. Deemed by the investigator to be able to understand and comply with the study requirements.
. Provided a signed and dated written informed consent form, along with any necessary personal data processing permissions, before any examination procedures.
Exclusion criteria
. Patients with severe cognitive impairments that would prevent them from understanding and completing the questionnaires independently
. Patients with severe visual impairments that would interfere with their ability to use mobile applications
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Time required to complete and process questionnaire
Timeframe: Baseline
2
Accuracy of AI-generated ICF coding compared to clinician coding
Timeframe: At study completion, approximately 3 months