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Mobility of Elderly Patients When Using the l'Ergonome Mobility Device

Evaluation of the Mobility of Elderly Patients (> 65 Years) When Using the l'Ergonome Mobility Device: a Randomized, Monocentric Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01746433
Acronym
L'ERGONOME
Enrollment
37
Registered
2012-12-11
Start date
2013-11-30
Completion date
2014-01-31
Last updated
2015-03-26

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

Conditions

Elderly, Supine Position

Brief summary

The main objective of this study is to compare the percentage of patients that successfully pass from a laying position to a sitting position in less than 10 seconds between study arms: * experimental arm: these patients will use the ERGONOME device to help them sit up * standard arm: these patients will use traditional hanging triangle bar to help them sit up

Detailed description

The secondary objectives of this study are to compare the following between study arms: * The average time (s) required to sit up * How the patient's center of gravity moves in relation to a fixed axis

Interventions

OTHERSitting up

The patient is positioned on a Winncare type bed dressed with a pressure-sensor sheet and equipped with either a hanging triangle bar (supporting arm of the bar is adjusted to 30 degrees) or an ERGONOME device according to randomization. The patient is first installed on the bed in a strictly supine position, the pelvis centered, and the greater trochanter over the fold of the backrest. The investigator then gives instructions on how to use the randomized device (correct hand placement). The patient is asked to sit up twice (two consecutive attempts). The first attempt is a learning attempt. The observations necessary for this study will be taken on the second attempt. Thus the second sitting attempt is timed, video-taped and recorded via the pressure-sensor sheet beneath the patient.

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* The patient must have given his/her informed and signed consent * The patient must be insured or beneficiary of a health insurance plan * The patient must be in stable medical condition (no complications for the last 10 days) * The patient is incapable of changing from a laying position to a sitting position by his/herself in \<10 secondes, and requires help for such movement * The patient has a sitting-balance score \> 2/4 (Brun et al 1991: Actual Rééduc Réadaptat: (16):412-7))

Exclusion criteria

* The patient is in an exclusion period determined by a previous study * The patient is under judicial protection, under tutorship or curatorship * The patient refuses to sign the consent * It is impossible to correctly inform the patient * The patient has fractured vertebrae or pelvis * The patient has a weak heart * The patient has joint pain localized to the dorso-lumbar region * The patient has behavioral disorders (opposition, agitation, dementia) * The patient has a medical prescription for physical restraint by bed rails. * The patient is incapable of understanding the utility of the proposed technical aide, and using it for rolling and sitting up (notion of compliance).

Design outcomes

Primary

MeasureTime frameDescription
Successful transition from a laying position to a sitting positionBaseline (day 0)yes/no

Secondary

MeasureTime frameDescription
Time needed to sit upbaseline (day 0)(minutes) The time needed to sit up is defined as follows: * The minimum time recorded for two attempts in the Hanging Triangle Bar group * The maximum time recorded for two attempts in the Ergonome group
Shift in the patient's center of mass (cm)baseline (day 0)Shift in the patient's center of mass away from the x-axis of a pressure-sheet placed on the bed.

Countries

France

Outcome results

None listed

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