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Evaluation of the Impact of Touch Relaxation in Sedated Intubated Patients Hospitalized in Intensive Care at Niort Hospital (ETDR)

C

Centre Hospitalier de Niort

Status

Enrolling

Conditions

Reaction Anxiety
Difficult or Failed Intubation

Treatments

Other: this arm will received relaxing touch (hands, feet, head) during 30 minutes twice a day

Study type

Interventional

Funder types

Other

Identifiers

NCT06346119
PI-2023-01

Details and patient eligibility

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.

Enrollment

72 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

72 participants in 2 patient groups

control
No Intervention group
Description:
this arm will not received relaxing touch. It's a control arm
Experimental
Experimental group
Description:
this arm will received relaxing touch twice a day
Treatment:
Other: this arm will received relaxing touch (hands, feet, head) during 30 minutes twice a day

Trial contacts and locations

1

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Central trial contact

Jean Marc M. Le Guevel, Nurse coordinator

Data sourced from clinicaltrials.gov

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