Barriers to Physical Activity in Patients With Cognitive, Neuromotor or Sensory Impairments During Aging

Disability or Chronic Disease Leading to Disablement Clinical Trial

— NO-BARRIERS  

Official title:

Barriers to Physical Activity in Patients With Cognitive, Neuromotor or Sensory Impairments During Aging

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05294068
• Other study ID #: 2022-001
• Status: Recruiting
• 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
• 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.

Related Conditions & MeSH terms

• Chronic Disease
• Disability or Chronic Disease Leading to Disablement

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