CClinicalTrials.gg
RecruitingNCT05294068NO-BARRIERSUpdated Apr 19, 2023

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

An observational study in Disability or Chronic Disease Leading to Disablement, sponsored by Institut de Sante Parasport Connecte Synergies. Recruiting at 1 site in France. Open to participants aged 6 Years and older. Per ClinicalTrials.gov, last updated 2023-04-19.

Sponsored by Institut de Sante Parasport Connecte Synergies · Observational

From the registry’s dates

  • Started Apr 2022; still recruiting 4 years 6 months later.
Study type
Observational
Model
Cohort
Time perspective
Other
Enrollment
1,000
Ages
6 Years and older
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Disability or Chronic Disease Leading to Disablement

Browse trials for

Keywords

  • Physical activities
  • Barriers
  • Disability
03

In context

Chronic Disease

990 studies on the registry are indexed under Chronic Disease; 178 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 419 across 249 observational studies indexed under Chronic Disease.

Browse Chronic Disease studies →

Lead sponsor

Institut de Sante Parasport Connecte Synergies is the lead sponsor of 7 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Subjects with cognitive, neuromotor or sensory impairments.

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

Exclusion Criteria:

  • Under court protection.
05

Study design

Observational model
Cohort
Time perspective
Other
Enrollment
1,000 participants (estimated)
Target follow-up
5 Years
Patient registry
Yes

Groups and cohorts

  • All subjects with cognitive impairments

    Other: standard of care for patients with cognitive impairments

  • All subjects with neuromotor impairments

    Other: standard of care for patients with neuromotor impairments

  • All subjects with sensory impairments

    Other: standard of care for patients with sensory impairments

Interventions

  • Otherstandard of care for patients with cognitive impairments

    clinical examination, radiological, biological and physiological examinations.

  • Otherstandard of care for patients with neuromotor impairments

    clinical examination, radiological, biological and physiological examinations.

  • Otherstandard of care for patients with sensory impairments

    clinical examination, radiological, biological and physiological examinations.

06

What researchers measure

Primary outcomes

  1. Changes of barriers to physical activity during aging

    Questionnaires assessing barriers and facilitators to physical activity (ex: BPAQ)

    Time frame: through study completion, an average of 1 year

Secondary outcomes

  1. Changes of physical activity level during aging

    Questionnaires assessing physical activity levels (ex: PASPID)

    Time frame: through study completion, an average of 1 year

  2. Characteristics of medical and medico-social therapies implemented to limit barriers to physical activity

    Number and description of medical and medico-social therapies

    Time frame: through study completion, an average of 1 year

  3. 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

    Time frame: through study completion, an average of 1 year

  4. 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

    Time frame: through study completion, an average of 1 year

  5. Evolution of comorbidities during aging

    Prevalence of comorbidities (e.g. obesity, diabetes, hypertension, sleep apnea, ...)

    Time frame: through study completion, an average of 1 year

  6. Evolution of exercise stress tests results during aging

    Stress tests results

    Time frame: through study completion, an average of 1 year

07

Study locations

1 of 1 sites recruiting
  • Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP
    Garches, 92380, France
    • Vincent T. Carpentier · Contact
    • François Genêt · Principal investigator
    • Constance Amelon-Petit · Sub investigator
    • Vincent T. Carpentier · Sub investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 19, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05294068
Lead sponsor
Institut de Sante Parasport Connecte Synergies
Collaborators
Assistance Publique - Hôpitaux de Paris
Responsible party
Sponsor
First posted
Mar 24, 2022
Start date
Apr 1, 2022
Primary completion
Feb 1, 2032 (estimated)
Completion
Feb 1, 2034 (estimated)
Last update
Apr 19, 2023

Study contacts

François Genêt, MD-PhD
Contact
francois.genet@aphp.fr
+33 1 47 10 70 82
Vincent T Carpentier, MD-MSc
Contact
vincent.carpentier@ispc-synergies.org
+33 1 47 10 70 82
François Genêt, MD-PhD
principal investigator · Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP, 92380 Garches, France
Vincent T Carpentier, MD-MSc
study director · Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP, 92380 Garches, France

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion