Actively Recruiting
Neuro-Orthopaedic Disorders During Aging in Patients With Neuromotor Disability
Led by Institut de Sante Parasport Connecte Synergies · Updated on 2022-12-23
2000
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
Sponsors
I
Institut de Sante Parasport Connecte Synergies
Lead Sponsor
A
Assistance Publique - Hôpitaux de Paris
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying how neuro-orthopedic disorders develop and affect people with neuromotor disabilities as they age. This includes patients with neurological damage from birth or injury affecting the spinal cord, brain, or peripheral nerves. The study aims to understand the long-term changes in these disorders, their impact on daily function, related health problems, and treatments used, as this information is currently limited. This observational study collects data from patients treated at a university hospital's Neuro Orthopaedic Unit within the Physical Medicine and Rehabilitation Department. Participants receive standard care involving clinical, radiological, biological, and physiological examinations. Researchers review medical records to gather detailed information about each patient's condition and treatments. Participants will be monitored for about one year to observe changes in mobility and other aspects such as fall and fracture rates, surgeries, use of orthoses and prostheses, physical activity levels, comorbidities, medications, and pressure sores. The study uses these measures to track the natural progression of their disorders and effects of care during aging.
CONDITIONS
Brief Title
Neuro-Orthopaedic Disorders During Aging in Patients With Neuromotor Disability
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 18 years old or older
- Treated in the Neuro Orthopaedic Unit of the Physical Medicine and Rehabilitation Department at a university hospital
- Have a neuromotor disability
- No opposition to enrollment from the patient or legally authorized close relative if the patient cannot consent
- Affiliated to a social security scheme
You will not qualify if you...
- Under court protection
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Approximately 1 year
Participants who undergo routine care are observed through collection of clinical, radiological, biological, and physiological data related to their neuromotor disability and aging.
Visits as part of routine healthcare over the study duration
Trial Site Locations
Total: 1 location
1
Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP
Garches, France, 92380
Actively Recruiting
Research Team
F
François Genêt, MD-PhD
V
Vincent T Carpentier, MD-MSc
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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