Pain
Conditions
Keywords
65 years old
Brief summary
The purpose of the project is to validate the use of Pain Monitor™ device, not invasive and simple of employment, for old people able to answer to a digital scale of pain intensity. The main objective is to develop and to validate a model of prediction of the pain in old subject at the time of the care, using the measure of variation of the skin conductance.
Interventions
DEVICEPain Monitor™
Pain measured by Pain Monitor™
Sponsors
Hopital Foch
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* hospitalized patient; * patient over 65 years of age; * communicating, without cognitive impairment; * having to undergo an act presumed to be painful during which the patient's mobility is limited: nursing care (removal of a drain, dressing of a chronic wound, urinary catheterization, etc.), medical examination, etc.; * benefiting from a social security scheme or having rights; * having given their prior informed written consent; * person able to read.
Exclusion criteria
* cutaneous anomaly on the site of measure; * pacemaker or internal defibrillator; * extremities twitching; * Treated by neostigmine.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation between Number of pics of skin conductance per second measured by Pain Monitor™ device with Numerical visual scale score for pain | 14 days |
Secondary
| Measure | Time frame |
|---|---|
| Hospital Anxiety and Depression (HAD) score | 14 days |
| Percentage of efficient poses of Pain Monitor | 14 days |
| Percentage of patient refusal to use of the Pain monitor | 14 days |
Countries
France
Outcome results
None listed