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Preliminary Study Leading to Prevention of Pressure Ulcers by the Use of an On-board Device : Ergonomic Assessment of Wheelchair-seat Pressures in Spinal Cord Injured (SCI) Patients ( PRESDIE)

Preliminary Study Leading to Prevention of Pressure Ulcers by the Use of an On-board Device : Ergonomic Assessment of Wheelchair-seat Pressures in Spinal Cord Injured (SCI) Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01834417
Acronym
PRESDIE
Enrollment
90
Registered
2013-04-17
Start date
2013-04-18
Completion date
2020-01-31
Last updated
2020-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pressure Ulcer

Keywords

Pressure ulcer, spinal cord injury, on-board device

Brief summary

Analysis of stored seat-pressures in SCI patients during a 4-week use of an on-board device. During this period, patients write in an agenda noteworthy events that could occur while they're using their wheelchair. A control is done every week and the device can be changed until it is returned at the end of the study period.

Detailed description

* inclusion visit : recovery of the signed informed-consent form, clinical examination, skin control, seat-pressures control, device 9-position control, delivery of the agenda for noteworthy events * 3 follow-up visits : noteworthy events check, skin control, cushioncloth control, device 9-position control * return visit : device return, agenda return, skin control, seat-pressures control

Interventions

DEVICETexiMat

Sponsors

Nantes University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

: * Patient is male or female, aged ≥ 18 * Patient accepting the initial assessment and the following visits during the protocol * Written informed consent has been obtained * Patient having a social assurance * Spinal cord injury ≤ C6 stable Spinal cord trauma \> 1 an * Main mode of ambulation : own manual wheelchair

Exclusion criteria

: * Aged ≤ 18 * Adults under guardianship * Patients do not speak French, refusing or unable to be followed * Pregnant or lactating women * Person deprived of their liberty by judicial or administrative decision * Person hospitalised without consent * Pelvic pressure ulcer ongoing * Cognitive disorder incompatible with the use of the device, understanding and conduct of the study

Design outcomes

Primary

MeasureTime frameDescription
Intra- and inter-patients variability of stored pressures for the whole included population Intra- and inter-patients variability of stored pressures for the whole included population4 weeksIntra- and inter-patients variability of stored pressures for the whole included population Measured at the end of the study Each topic will be equipped with a layer of pressure sensors 32x32. The pressure maps are stored every second rule, which will be of the order of 30 000 maps daily. For each topic, we will be able to calculate the frequency and location of peak pressure

Secondary

MeasureTime frameDescription
Intra- and inter-patients variability of stored pressures for subpopulations4 weeksIntra- and inter-patients variability of stored pressures for subpopulations : * quadriplegic vs paraplegic * according to high-risk areas for pressure ulcers * according to noteworthy events Each topic will be equipped with a layer of pressure sensors 32x32. The pressure maps are stored every second rule, which will be of the order of 30 000 maps daily. For each topic, we will be able to calculate the frequency and location of peak pressure Measured at the end of the study

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026