Neuro-Orthopaedic Disorders During Aging in Patients With Neuromotor Disability

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorInstitut de Sante Parasport Connecte Synergies

About this trial

People with neuromotor disability (i.e. following an inborn or acquired spinal cord, cerebral or peripheral neurological lesion) are at risk of worsening their neuro-orthopaedic disorders during aging, including fracture risk. Nevertheless, at the present time, the natural evolution of their neuro-orthopedic disorders and the long-term functional impact of their medical and surgical treatments is unknown.

The aim of this study is to describe neuro-orthopedic disorders during aging of patients with neuromotor disability, their functional repercussions, their comorbidities and the therapeutic strategies used.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients >= 18 years old ;

Treated in the Neuro Orthopaedic Unit (UPOH) of the Physical Medicine and Rehabilitation Department of our university hospital ;

Having a neuromotor disability ;

No opposition to be enrolled in the study from the patient, or from a legally authorized close relative if the patient's state of health does not allow it ;

Disqualifiers

Under court protection.

Trial population

Subjects with neuromotor disability

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

  • standard of care for patients with neuromotor disability

    Other intervention

    clinical examination, radiological, biological and physiological examinations.

Treatment groups

2,000 Participants
are divided into 1 treatment group
Group A: All subjects with neuromotor disability1 intervention

Trial outcomes

Primary outcomes

1

Evolution of mobility during aging

Walking range

Time frame
Through study completion, an average of 1 year

Secondary outcomes

1

Prevalence of falls and fractures

Number and description of falls and fractures

Time frame
Through study completion, an average of 1 year
2

Characteristics of infiltrative procedures and surgeries

Number and description of infiltrative procedures and surgeries

Time frame
Through study completion, an average of 1 year
3

Changes of devices (orthoses and prostheses) and technical aids used during aging

Number and description of devices (orthoses and prostheses) and technical aids

Time frame
Through study completion, an average of 1 year
4

Changes of physical activity, as well as barriers and facilitators to physical activity, during aging

Questionnaires assessing physical activity levels (ex: PASPID) and barriers and facilitators to physical activity (ex: BPAQ)

Time frame
Through study completion, an average of 1 year

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Institut de Sante Parasport Connecte Synergies

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Collaborator