video recording for Parkinson's (NCT07392411)
Distinguish Parkinson from similar disorders
- Trial ID
- NCT07392411
- Official Title
- Study on Artificial Intelligence-Based Facial and Speech-Related Patterns in Parkinson's Disease and Their Digital Biomarkers
- Goal
- Distinguish Parkinson from similar disorders
- Status
- RECRUITING
- Sponsor
- Beijing Tiantan Hospital
- Study Type
- OBSERVATIONAL
- Enrollment
- 720 participants
- Conditions
- Parkinson's Disease, Progressive Supranuclear Palsy(PSP), Multiple System Atrophy, Healthy Control
- Interventions
- video recording
Summary For Families
The goal is to see if computer analysis of facial expressions and speech can be turned into digital tools that help diagnose and tell apart Parkinson's disease and similar disorders. The team records videos of faces and audio of speech and uses artificial intelligence to look for patterns that signal each condition. They are enrolling adults about 18 to 75 years old, including people with Parkinson's at early or mid-to-late stages, people with progressive supranuclear palsy or multiple system atrophy, and healthy volunteers, and everyone must agree to the video and audio recording. People with major past brain injuries or conditions, very poor performance on a standard thinking test, or severe involuntary movements that would interfere with recording are not eligible.
Locations
- 首都医科大学附属北京天坛医院, Beijing, Beijing Municipality, China
Frequently Asked Questions
- What is this trial testing?
- This trial is studying video recording. The goal is to see if computer analysis of facial expressions and speech can be turned into digital tools that help diagnose and tell apart Parkinson's disease and similar disorders. The team records videos of faces and audio of speech and uses artificial intelligence to look for patterns that signal each condition. They are enrolling adults about 18 to 75 years old, including people with Parkinson's at early or mid-to-late stages, people with progressive supranuclear palsy or multiple system atrophy, and healthy volunteers, and everyone must agree to the video and audio recording. People with major past brain injuries or conditions, very poor performance on a standard thinking test, or severe involuntary movements that would interfere with recording are not eligible.
- Who can participate?
- Participants must be between 15 Years and 75 Years.
- Where is this trial located?
- This trial is recruiting at 1 location.
- Does it cost anything to join?
- You are never charged a fee to join a legitimate clinical trial, and the study treatment and study-specific tests are provided by the trial sponsor at no charge. In the US, routine care you would receive anyway can still be billed to you or your insurance; coverage rules differ by country, and trials in the UK and Canada usually run through public health systems. Travel, parking, and time are real costs, and some trials reimburse them while others do not. Before enrolling, ask the study coordinator to explain in writing what is and is not covered.
- How long does the trial last?
- This trial is estimated to last approximately 3 years and 5 months.
- Can I leave the trial if I change my mind?
- Yes. You can withdraw from any clinical trial at any time, for any reason, without affecting your standard medical care. Trials are voluntary by law. The team may ask if you are willing to do a brief exit visit so they can collect safety information, but you are not obligated.
- Can my spouse or care partner come with me to visits?
- In most cases yes, and it is often encouraged. Care partners can help with notes, questions, and getting home safely after a long visit. Some study assessments do need to happen one on one, but care partners are usually welcome for the rest of the appointment.
- Will I get a placebo in this trial?
- This is an observational study, so there is no placebo and no experimental treatment is assigned. Researchers observe and collect information while you continue your usual care.
- What procedures are involved in this trial?
- Based on the protocol, this trial involves: Surgical procedure (invasive); Walking & movement tests (non-invasive). Confirm the full schedule with the study coordinator.