- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05294068
Barriers to Physical Activity in Patients With Cognitive, Neuromotor or Sensory Impairments During Aging (NO-BARRIERS)
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.
Study Overview
Status
Detailed 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.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
-
Garches, France, 92380
- Recruiting
- Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
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 Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
All subjects with cognitive impairments
|
clinical examination, radiological, biological and physiological examinations.
|
All subjects with neuromotor impairments
|
clinical examination, radiological, biological and physiological examinations.
|
All subjects with sensory impairments
|
clinical examination, radiological, biological and physiological examinations.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Changes of barriers to physical activity during aging
Time Frame: through study completion, an average of 1 year
|
Questionnaires assessing barriers and facilitators to physical activity (ex: BPAQ)
|
through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Changes of physical activity level during aging
Time Frame: through study completion, an average of 1 year
|
Questionnaires assessing physical activity levels (ex: PASPID)
|
through study completion, an average of 1 year
|
Characteristics of medical and medico-social therapies implemented to limit barriers to physical activity
Time Frame: through study completion, an average of 1 year
|
Number and description of medical and medico-social therapies
|
through study completion, an average of 1 year
|
Characteristics of the medical and medico-social therapies implemented to limit disability-related underperformance factors for competitive sports
Time Frame: through study completion, an average of 1 year
|
Number and description of medical and medico-social therapies
|
through study completion, an average of 1 year
|
Characteristics of devices (orthoses, prostheses, etc.) and technical aids used to facilitate the practice of physical activity
Time Frame: through study completion, an average of 1 year
|
Number and description of devices (orthoses and prostheses) and technical aids
|
through study completion, an average of 1 year
|
Evolution of comorbidities during aging
Time Frame: through study completion, an average of 1 year
|
Prevalence of comorbidities (e.g.
obesity, diabetes, hypertension, sleep apnea, ...)
|
through study completion, an average of 1 year
|
Evolution of exercise stress tests results during aging
Time Frame: through study completion, an average of 1 year
|
Stress tests results
|
through study completion, an average of 1 year
|
Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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