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Neuro-Orthopaedic Disorders During Aging in Patients With Neuromotor Disability

Neuro-Orthopaedic Disorders During Aging in Patients With Neuromotor Disability

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05294029
Acronym
NO-AGING
Enrollment
2000
Registered
2022-03-24
Start date
2022-05-01
Completion date
2034-02-01
Last updated
2022-12-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Disability or Chronic Disease Leading to Disablement

Keywords

Neuromotor Disability, Neuro-Orthopaedics

Brief summary

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.

Detailed description

This is an ambispective, monocentric, cohort study of subjects with neuromotor disability followed in a Physical Medicine and Rehabilitation Department. All consecutive eligible inpatient and outpatient subjects treated in the Neuro Orthopaedic Unit (UPOH) of the Physical Medicine and Rehabilitation Department of our university hospital will be included. Data will be collected from the patients' medical records, in particular data related to their clinical, radiological, biological and physiological examinations.

Interventions

OTHERstandard of care for patients with neuromotor disability

clinical examination, radiological, biological and physiological examinations.

Sponsors

Assistance Publique - Hôpitaux de Paris
CollaboratorOTHER
Institut de Sante Parasport Connecte Synergies
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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 ; * Affiliation to a social security scheme.

Exclusion criteria

* Under court protection.

Design outcomes

Primary

MeasureTime frameDescription
Evolution of mobility during agingThrough study completion, an average of 1 yearWalking range

Secondary

MeasureTime frameDescription
Prevalence of falls and fracturesThrough study completion, an average of 1 yearNumber and description of falls and fractures
Characteristics of infiltrative procedures and surgeriesThrough study completion, an average of 1 yearNumber and description of infiltrative procedures and surgeries
Changes of devices (orthoses and prostheses) and technical aids used during agingThrough study completion, an average of 1 yearNumber and description of devices (orthoses and prostheses) and technical aids
Prevalence of pressure soresThrough study completion, an average of 1 yearNumber and description of pressure sores
Evolution of comorbidities during agingThrough study completion, an average of 1 yearPrevalence of comorbidities (e.g. obesity, diabetes, hypertension, sleep apnea, ...)
MedicationThrough study completion, an average of 1 yearMedication list
Changes of physical activity, as well as barriers and facilitators to physical activity, during agingThrough study completion, an average of 1 yearQuestionnaires assessing physical activity levels (ex: PASPID) and barriers and facilitators to physical activity (ex: BPAQ)

Countries

France

Contacts

Primary ContactFrançois Genêt, MD-PhD
francois.genet@aphp.fr+33 1 47 10 70 82
Backup ContactVincent T Carpentier, MD-MSc
vincent.carpentier@ispc-synergies.org+33 1 47 10 70 82

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026