Effectiveness of HYPNOsis Masks During Botulinum TOXin Injections in Idiopathic Overactive Bladder(HypnoTox) (HypnoTox)
Primary Purpose
Idiopathic Overactive Bladder
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
HyPNOS self-hypnosis mask from DREAMINZZ
Sponsored by
About this trial
This is an interventional supportive care trial for Idiopathic Overactive Bladder focused on measuring hypnosis mask, idiopathic overactive bladder, pain, anxiety
Eligibility Criteria
Inclusion Criteria:
- Woman with non-neurological overactive bladder, confirmed by urodynamic assessment and cystoscopy, having resisted a well-conducted pharmacological treatment (trials of various anticholinergics).
- Age over 18 years
- Having understood the study and agreed to participate (signing of informed consent)
- Beneficiary of a health insurance plan
Exclusion Criteria:
- Neurological patient: tetraplegic, paraplegic, multiple sclerosis for a reliable pain assessment
- Patients who have already been injected with botulinum toxin in the treatment of this pathology.
- Psychiatric pathology at risk of decompensation with self-hypnosis
- Patients who are difficult to assess because of a psychological disorder that does not allow them to answer questionnaires and pain assessment scales
- Patients under court protection, guardianship or curatorship
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
control arm
interventional arm
Arm Description
conventional anaesthesia The botulinum toxin injection procedure will be carried out in the standard way, according to the recommendations applicable in France, and after local anaesthesia.
conventional anaethesia and use of the self-hypnosis mask The mask and the helmet are positioned and activated 10 minutes before the procedure, with the "travel to india" programme chosen because it was developed for pain management and its duration is compatible with the procedure (25 minutes).
Outcomes
Primary Outcome Measures
Pain felt at the time of the injections
Measured by a Visual Analogue Scale (VAS) rated from 0 to 100 millimetres
Secondary Outcome Measures
Anxiety
Measured by the STAI Forme Y-A which assesses the state of anxiety at a given time
Pain felt on insertion of the cystoscope
Measured by a Visual Analogue Scale (VAS) rated from 0 to 100 millimetres
Occurrence of complications
Hematuria, Acute Urine Retention and Urinary Tract Infection
Success of the 50IU procedure
Assessed by the doctor
Full Information
NCT ID
NCT05352945
First Posted
April 25, 2022
Last Updated
May 2, 2022
Sponsor
Centre Hospitalier de Roubaix
1. Study Identification
Unique Protocol Identification Number
NCT05352945
Brief Title
Effectiveness of HYPNOsis Masks During Botulinum TOXin Injections in Idiopathic Overactive Bladder(HypnoTox)
Acronym
HypnoTox
Official Title
Effectiveness of HYPNOsis Masks in the Management of Pain and Anxiety During Botulinum TOXin Injections in the Treatment of Idiopathic Overactive Bladder: a Multicenter Randomized Parallel Group Study.
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 2022 (Anticipated)
Primary Completion Date
February 2024 (Anticipated)
Study Completion Date
June 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier de Roubaix
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Monocenter, prospective, randomized, parallel group study (1:1) evaluating the efficacy of self-hypnosis performed by mask on pain and anxiety in patients receiving botulinum toxin injections in the treatment of idiopathic overactive bladder refractory to conventional pharmacological treatment.
Patients will be randomized into two groups before injection:
Group 1: conventional anesthesia
Group 2: conventional anesthesia and use of the self-hypnosis mask
At the end of the procedure, the patient will express the pain felt thanks to the VAS (Visual Analog Scale) and will answer a questionnaire of anxiety (STATE-TRAIT Anxiety Inventory).
Detailed Description
Day 0: 1st consultation for overactive bladder refractory to drug treatment: verification of inclusion and non-inclusion criteria. Proposal of the study to the patient and handing over of the information note relating to the study.
D15: Collection of consent and randomisation - execution of the procedure
Botulinum toxin injection procedure
Control arm: conventional anaesthesia The botulinum toxin injection procedure will be carried out in a standard manner, according to French guidances, and after local anaesthesia as specified below.
For the procedure, the patient will be hospitalised in a urological day hospital. She must have a sterile cytobacteriological exam of urine 10 days before the procedure or be on antibiotics, and must not have any coagulation problems.
A local anaesthetic is given 30 minutes before the procedure according national guidances.
Experimental arm: conventional anaesthesia and use of the self-hypnosis mask
Same procedure as described for the control arm with the addition of the self-hypnosis mask during the procedure:
The mask and the headphones are positioned and activated 10 minutes before the procedure, with the program "travel to India" chosen because it was developed for pain management and of a duration compatible with the procedure (25 minutes).
A short presentation acting as a pre-hypnotic speech can introduce the use of the mask on a patient in order to orientate the effects in the desired goal (analgesia, relaxation, etc.).
After connecting the mask to the mobile application, the caregiver will set the appropriate program for the treatment, place the mask over the patient's closed eyes, place the headphones over the patient's ears as well and start the session in question.
Following the procedure, monitoring in the day hospital and evaluation at 30 minutes of the procedure by a trained nurse, of the pain felt during the insertion of the cystoscope and during the injections by VAS.
Completion of the STATE-TRAIT Anxiety Inventory test.
D45: Regular monitoring consultation with evaluation of treatment effectiveness. Collection of data concerning complications (haematuria, urine retention and urinary tract infection). Discharge from the study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Overactive Bladder
Keywords
hypnosis mask, idiopathic overactive bladder, pain, anxiety
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients newly eligible for treatment of idiopathic overactive bladder with botulinum toxin injection will be randomised into two groups before injection:
Group 1: conventional anaesthesia
Group 2: conventional anaesthesia and use of self-hypnosis mask
Masking
None (Open Label)
Masking Description
Blinding is not possible with the self-hypnosis mask as it emits sounds and lights for its effect.
Allocation
Randomized
Enrollment
70 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
control arm
Arm Type
No Intervention
Arm Description
conventional anaesthesia
The botulinum toxin injection procedure will be carried out in the standard way, according to the recommendations applicable in France, and after local anaesthesia.
Arm Title
interventional arm
Arm Type
Experimental
Arm Description
conventional anaethesia and use of the self-hypnosis mask
The mask and the helmet are positioned and activated 10 minutes before the procedure, with the "travel to india" programme chosen because it was developed for pain management and its duration is compatible with the procedure (25 minutes).
Intervention Type
Device
Intervention Name(s)
HyPNOS self-hypnosis mask from DREAMINZZ
Intervention Description
The use of the HyPNOS self-hypnosis mask from DREAMINZZ allows patients to immerse themselves in a state of self-hypnosis.
A Hypnos session is a narrative accompanied by spatialized sounds (3D) and ambiance for an immersive experience.
We aim to evaluate the use of the HyPNOS mask in the management of pain and anxiety in botulinum toxin injections
Primary Outcome Measure Information:
Title
Pain felt at the time of the injections
Description
Measured by a Visual Analogue Scale (VAS) rated from 0 to 100 millimetres
Time Frame
During the botulinum toxin injections
Secondary Outcome Measure Information:
Title
Anxiety
Description
Measured by the STAI Forme Y-A which assesses the state of anxiety at a given time
Time Frame
During the botulinum toxin injections
Title
Pain felt on insertion of the cystoscope
Description
Measured by a Visual Analogue Scale (VAS) rated from 0 to 100 millimetres
Time Frame
During insertion of the cystoscope
Title
Occurrence of complications
Description
Hematuria, Acute Urine Retention and Urinary Tract Infection
Time Frame
During the 7 days post-procedure
Title
Success of the 50IU procedure
Description
Assessed by the doctor
Time Frame
At 1 month post-procedure
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Woman with non-neurological overactive bladder, confirmed by urodynamic assessment and cystoscopy, having resisted a well-conducted pharmacological treatment (trials of various anticholinergics).
Age over 18 years
Having understood the study and agreed to participate (signing of informed consent)
Beneficiary of a health insurance plan
Exclusion Criteria:
Neurological patient: tetraplegic, paraplegic, multiple sclerosis for a reliable pain assessment
Patients who have already been injected with botulinum toxin in the treatment of this pathology.
Psychiatric pathology at risk of decompensation with self-hypnosis
Patients who are difficult to assess because of a psychological disorder that does not allow them to answer questionnaires and pain assessment scales
Patients under court protection, guardianship or curatorship
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Camille Trouillet, PM
Phone
03.20.99.31.31
Email
camille.trouillet@ch-roubaix.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Louise M Van Sante, CRA
Phone
03.20.99.31.31
Email
louise.vansante@ch-roubaix.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
François Pecoux, Doctor
Organizational Affiliation
CH Roubaix
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
The database created will remain the property of the Hospital Center of Roubaix. The Hospital Center of Roubaix will carry out the main publication of the research.
Once this has been done, the investigating centres that participated in the research can request access to the database for the purpose of secondary publications.
If the request is successful, the database will be transmitted securely and completely anonymously to the applicant.
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Effectiveness of HYPNOsis Masks During Botulinum TOXin Injections in Idiopathic Overactive Bladder(HypnoTox)
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