Evaluation of the Impact of Touch Relaxation in Sedated Intubated Patients Hospitalized in Intensive Care at Niort Hospital
Recruiting · NCT06346119 · Interventional (participants receive a specific treatment) · Lead sponsor: Centre Hospitalier de Niort
View the official record on ClinicalTrials.gov →Interventions studied
this arm will received relaxing touch (hands, feet, head) during 30 minutes twice a day
What this trial is about
This is a randomized prospective study. This objective is the impact of "relaxing touch" on the use of chemical restraint for patients in intensive care from the lifting of sedation until extubation.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Male or female over 18 years of age
- Intubated and sedated man or woman
- Extubation within 48 hours
- Intubation of more than 48 hours in total
- Patient in intensive care at Niort hospital
- The trusted person or referent accepting the patient's participation
- Patient affiliated to the social security system
Exclusion criteria
- Known pregnancy
- Patient who refused to participate in the study after the fact
- Patients under long-term antidepressant treatment (treatment longer than 3 months)
- Patients under guardianship or curatorship
- Patient deprived of liberty
- Skin lesions on the hands/feet/head (wounds, erythema, burns, bedsores, phlyctenes)
- Inclusion in another clinical study
Where it is running
1 location listed.
- Centre Hospitalier de Niort - Niort, France