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NCT Number: NCT05294068

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

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.

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Key information

Age range

6 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP

Garches, 92380, France

Location status: Recruiting

Location contact

Constance Amelon-Petit

SUB_INVESTIGATOR

François Genêt

PRINCIPAL_INVESTIGATOR

Vincent T. Carpentier

CONTACT

Vincent T. Carpentier

SUB_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

standard of care for patients with cognitive impairments

Other

clinical examination, radiological, biological and physiological examinations.

standard of care for patients with neuromotor impairments

Other

clinical examination, radiological, biological and physiological examinations.

standard of care for patients with sensory impairments

Other

clinical examination, radiological, biological and physiological examinations.

Primary outcomes

  1. 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)

Secondary outcomes

  1. Changes of physical activity level during aging

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

    Questionnaires assessing physical activity levels (ex: PASPID)

  2. 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

  3. 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

  4. 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

  5. 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, ...)

  6. Evolution of exercise stress tests results during aging

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

    Stress tests results

Study contacts

Contact information is provided by the study sponsor or research team.

François Genêt, MD-PhD

CONTACT

[email protected]

+33 1 47 10 70 82

Vincent T Carpentier, MD-MSc

CONTACT

[email protected]

+33 1 47 10 70 82

Sponsors and collaborators

Lead sponsor

Institut de Sante Parasport Connecte Synergies

Other

Collaborators

  • Assistance Publique - Hôpitaux de Paris

Registry information

Acronym: NO-BARRIERS

Important dates

Study start
2022
Primary completion
2032
Study completion
2034
First posted
Mar 24, 2022
Registry last updated
Apr 19, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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