Physical Activity in People With Sequelae of Poliomyelitis

January 18, 2023 updated by: Institut de Sante Parasport Connecte Synergies

Physical Activity in People With Sequelae of Poliomyelitis : a Cross-sectional Study

People with disabilities are less physically active than the general population. At present, the physical activity level of people with poliomyelitis sequelae and their barriers to physical activity are unknown.

The aim of this study is to describe the physical activity level of people with poliomyelitis sequelae and their barriers to physical activity.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

This is a cross-sectional, monocentric, cohort study of subjects with poliomyelitis sequelae followed in a Physical Medicine and Rehabilitation Department.

All consecutive eligible outpatient subjects consulting to the Physical Medicine and Rehabilitation Department of our university hospital will be included.

Data will be collected from the patients' medical records, in particular data related to their clinical, radiological, biological and physiological examinations.

It is an ancillary study to the NO-AGING study.

Study Type

Observational

Enrollment (Anticipated)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • France
      • Garches, France, 92380
        • Recruiting
        • Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP
        • Sub-Investigator:
          • Marjorie Salga

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Subjects with poliomyelitis sequelae.

Description

Inclusion Criteria:

  • Consulting to the Physical Medicine and Rehabilitation Department of our university hospital
  • Having poliomyelitis sequelae
  • No opposition to be enrolled in the study from the patient
  • Affiliation to a social security scheme

Exclusion Criteria:

  • Disability that does not allow the completion of questionnaires
  • Acute intercurrent medical situation
  • Use of electric wheelchair
  • Under court protection.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
All subjects with poliomyelitis sequelae
Other: standard of care for patients with poliomyelitis sequelae
clinical examination, radiological, biological and physiological examinations.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Physical activity level
Time Frame: Baseline
Physical Activity Scale for Individuals with Physical Disabilities (PASIPD) Questionnaire
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Barriers of physical activity
Time Frame: Baseline
Barriers to Physical Activity Questionnaire for People with Mobility Impairments (BPAQ-MI)
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Institut de Sante Parasport Connecte Synergies

Collaborators

Assistance Publique - Hôpitaux de Paris

Investigators

  • Study Chair: Vincent T Carpentier, MD-MSc, Department of Physical Medicine and Rehabilitation, Raymond Poincaré Hospital, AP-HP, 92380 Garches, France

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2022

Primary Completion (Anticipated)

October 1, 2023

Study Completion (Anticipated)

December 1, 2023

Study Registration Dates

First Submitted

March 15, 2022

First Submitted That Met QC Criteria

March 26, 2022

First Posted (Actual)

March 31, 2022

Study Record Updates

Last Update Posted (Estimate)

January 19, 2023

Last Update Submitted That Met QC Criteria

January 18, 2023

Last Verified

January 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2022-003

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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