Use of Virtual Reality Mask or Music Therapy for Analgesia and Anxiolytic Purpose When Totally IVAD for Chemotherapy Under Local Anesthesia (REVCCI)

  • STATUS
    Recruiting
  • End date
    Dec 2, 2023
  • participants needed
    127
  • sponsor
    Institut Curie
Updated on 25 May 2022

Summary

Evaluate 2 medical devices on pain average and/or anxiety average in the totally Implanted Venous Access Device (IVAD) procedure under local anesthesia.

Description

Evaluate the efficacy of virtual reality and music therapy on pain average and/or anxiety average in the totally Implanted Venous Access Device (IVAD) procedure under local anesthesia.

Details
Condition Implanted Venous Access Device
Treatment REV : local anesthesia and virtual reality, MUS : local anesthesia and music therapy
Clinical Study IdentifierNCT04804735
SponsorInstitut Curie
Last Modified on25 May 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Patient aged between 18 and 85 years
Patient with cancer care and having a totally Implanted Venous Access Device (IVAD) procedure under local anesthesia for chemotherapy
Absence of anxiolytic premedication
Patient affiliated to social insurance
Absence of contra-indication to the use of virtual reality, music therapy instrument or local lidocaine anesthesia
Signed informed consent form

Exclusion Criteria

Patient already participated to this study
Patient deprived of liberty or under legal representative or under curatorship
Psychiatric disease enabling communication
Deafness or visual impairement
Patient under beta-blockers medication
Chronic pain present and not equilibrated before the measured procedure as > 3 by the NRS
Tracheotomy
Low cervical tumor, or bilateral low cervical adenopathies
Compression or jugular stenosis (uni or bilateral)
Jugular or subclavian thrombosis
Patient under anticoagulants medication or having hesmostasis troubles
Claustrophobia or thalassophobia inducing the possibility of rejecting the virtual reality mask or music therapy mask
Patients not speaking french
Pregnant and breastfeeding women
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

0/250

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note