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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01935687
Other study ID # P101006
Secondary ID
Status Completed
Phase N/A
First received March 4, 2013
Last updated November 17, 2017
Start date December 2012
Est. completion date July 2015

Study information

Verified date November 2017
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to validate an instrumented wheel such as a new biomedical device. The physicians will compare this instrumented wheel with another instrumentation "Ergometer roller", each patient will try the both instrumentations, physical and physiological parameters will be measured.

The increase rate of radial power during the cardiac stress test may be more important when the physicians use the instrumented wheel.


Description:

* The manual wheelchair is used by people for whom walking is difficult or impossible due to spinal cord lesions, neurological and muscular diseases, lower limb trauma, age …etc.

Although the wheelchair help to regain mobility, this made of displacement is nor natural nor well-to-do.

- The CIC-IT and TSR (Transmissions Services Roulements, Mérignac, France) improved the instrumented wheel, adaptable with all wheelchairs, with information wireless transmission.

- The primary objective of study is to validate the instrumented wheel of manual wheelchair such as a new device of evaluation of capacities of displacement in ecologic situation.

- The primary criteria is to compare the mechanical power calculated using instrumented wheel versus the power calculated using ergometer roller during protocol of standard cardio-respiratory stress test.

This study is interventional, mono-centric, controlled and crossover. The population concerned is patients with spinal cord injury (SCI) and users of manual wheelchair.

Number of subjects projected for the entire study: 62 patients The total duration of participation of each patient: 7 days ±2days


Recruitment information / eligibility

Status Completed
Enrollment 62
Est. completion date July 2015
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Age : 18-70 years.

- Spinal cord injured patient.

- User of manual wheelchair for daily locomotion (having at least 30/100 at displacement items of WST questionnaire) .

- Affiliation to a social security scheme or entitled.

- Informed consent dated and signed by subject or subject's legally acceptable representative (and investigator).

Exclusion Criteria:

- Cognitive troubles.

- Progressive diseases: Tumoral, infectious, inflammatory and associated pathologies: brain injury, amputation.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Using of instrumented wheel
Using of instrumented wheel
Using of ergometer roller
Using of ergometer roller

Locations

Country Name City State
France Djamel Bensmail Garches Hauts-de-Seine

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Other Physiological parameters using instrumented wheel Heart rate, VO2 and Borg score. 6 min
Other Physiological parameters using ergometer roller Heart rate, VO2 and Borg score. 15 min
Primary Mechanical power calculated by instrumented wheel and ergometer roller. Comparison between mechanical power calculated by the instrumented wheel and mechanical power calculated by ergometer roller. 20 min
Secondary Efficient fraction of total power calculated using instrumented wheel Tangential power / total power 6 min
Secondary Efficient fraction of total power calculated using ergometer roller Tangential power / total power 15 min
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