Barriers to Physical Activity in Patients With Cognitive, Neuromotor or Sensory Impairments During Aging
NCT ID: NCT05294068
Last Updated: 2023-04-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
1000 participants
OBSERVATIONAL
2022-04-01
2034-02-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Fragility and Adapted Physical Activity
NCT02690402
An INtervention TO Improve MOBility of Older Hospitalized Patients
NCT05639231
Prevention of the Older Adult's Loss of Autonomy at Home Through a Targeted Physical Exercise Program
NCT03992222
Home-based Adapted Physical Activity in Anorexia Nervosa: a Feasibility Pilot Study
NCT05803707
Prospective Study and Analysis of Biomechanical Parameters of Human Movement Based on Disability Indicators in Older Adults
NCT05656690
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
OTHER
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
All subjects with cognitive impairments
standard of care for patients with cognitive impairments
clinical examination, radiological, biological and physiological examinations.
All subjects with neuromotor impairments
standard of care for patients with neuromotor impairments
clinical examination, radiological, biological and physiological examinations.
All subjects with sensory impairments
standard of care for patients with sensory impairments
clinical examination, radiological, biological and physiological examinations.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
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.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
6 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Assistance Publique - Hôpitaux de Paris
OTHER
Institut de Sante Parasport Connecte Synergies
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
François Genêt, MD-PhD
Role: PRINCIPAL_INVESTIGATOR
Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP, 92380 Garches, France
Vincent T Carpentier, MD-MSc
Role: STUDY_DIRECTOR
Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP, 92380 Garches, France
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP
Garches, , France
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Vincent T. Carpentier
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2022-001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.