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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05294068
Other study ID # 2022-001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 1, 2022
Est. completion date February 1, 2034

Study information

Verified date April 2023
Source Institut de Sante Parasport Connecte Synergies
Contact François Genêt, MD-PhD
Phone +33 1 47 10 70 82
Email francois.genet@aphp.fr
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

People with disabilities are less physically active than the general population. Their barriers to physical activity are multiple and include intrapersonal, organizational, societal and interpersonal reasons. Nevertheless, at present, the evolution of their barriers to physical activity and the short- and long-term impact of medical and medico-social treatments to limit them are unknown. The aim of this study is to describe barriers to physical activity, or disability-related underperformance factors in competitive sports, in patients with cognitive, neuromotor or sensory impairments during aging.


Description:

This is an ambispective, monocentric, cohort study of subjects with cognitive, neuromotor or sensory impairments followed in a Physical Medicine and Rehabilitation Department. All consecutive eligible outpatient subjects consulting to the Parasport Health Unit of the Physical Medicine and Rehabilitation Department of our university hospital will be included. Clinical activities related to the Parasport Health Unit and performed outside the hospital will also be included. Data will be collected from the patients' medical records, in particular data related to their clinical, radiological, biological and physiological examinations.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date February 1, 2034
Est. primary completion date February 1, 2032
Accepts healthy volunteers No
Gender All
Age group 6 Years and older
Eligibility Inclusion Criteria: - Patients >= 6 years old ; - Consulting to the Parasport Health Unit of the Physical Medicine and Rehabilitation Department of our university hospital ; - Having a neuromotor, cognitive or sensory impairment ; - 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, or from each of the holders of parental authority if a minor ; - Affiliation to a social security scheme. Exclusion Criteria: - Under court protection.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
standard of care for patients with cognitive impairments
clinical examination, radiological, biological and physiological examinations.
standard of care for patients with neuromotor impairments
clinical examination, radiological, biological and physiological examinations.
standard of care for patients with sensory impairments
clinical examination, radiological, biological and physiological examinations.

Locations

Country Name City State
France Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP Garches

Sponsors (2)

Lead Sponsor Collaborator
Institut de Sante Parasport Connecte Synergies Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes of barriers to physical activity during aging Questionnaires assessing barriers and facilitators to physical activity (ex: BPAQ) through study completion, an average of 1 year
Secondary Changes of physical activity level during aging Questionnaires assessing physical activity levels (ex: PASPID) through study completion, an average of 1 year
Secondary Characteristics of medical and medico-social therapies implemented to limit barriers to physical activity Number and description of medical and medico-social therapies through study completion, an average of 1 year
Secondary Characteristics of the medical and medico-social therapies implemented to limit disability-related underperformance factors for competitive sports Number and description of medical and medico-social therapies through study completion, an average of 1 year
Secondary Characteristics of devices (orthoses, prostheses, etc.) and technical aids used to facilitate the practice of physical activity Number and description of devices (orthoses and prostheses) and technical aids through study completion, an average of 1 year
Secondary Evolution of comorbidities during aging Prevalence of comorbidities (e.g. obesity, diabetes, hypertension, sleep apnea, ...) through study completion, an average of 1 year
Secondary Evolution of exercise stress tests results during aging Stress tests results through study completion, an average of 1 year
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