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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
Centre Hospitalier de Roubaix
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

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

    First Posted
    April 25, 2022
    Last Updated
    May 2, 2022
    Sponsor
    Centre Hospitalier de Roubaix
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    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.
    Citations:
    PubMed Identifier
    24548148
    Citation
    Zhang ZS, Wang XL, Xu CL, Zhang C, Cao Z, Xu WD, Wei RC, Sun YH. Music reduces panic: an initial study of listening to preferred music improves male patient discomfort and anxiety during flexible cystoscopy. J Endourol. 2014 Jun;28(6):739-44. doi: 10.1089/end.2013.0705. Epub 2014 Mar 31.
    Results Reference
    background
    PubMed Identifier
    19937315
    Citation
    Haylen BT, de Ridder D, Freeman RM, Swift SE, Berghmans B, Lee J, Monga A, Petri E, Rizk DE, Sand PK, Schaer GN. An International Urogynecological Association (IUGA)/International Continence Society (ICS) joint report on the terminology for female pelvic floor dysfunction. Int Urogynecol J. 2010 Jan;21(1):5-26. doi: 10.1007/s00192-009-0976-9. Epub 2009 Nov 25.
    Results Reference
    result
    PubMed Identifier
    25662706
    Citation
    Game X, Karsenty G, Ruffion A, Amarenco G, Ballanger P, Chartier-Kastler E, Cosson M, Costa P, Fatton B, Deffieux X, Haab F, Hermieu JF, Le Normand L, Saussine C, Denys P. [Idiopathic overactive bladder and BOTOX((R)): Literature review]. Prog Urol. 2015 Jun;25(8):461-73. doi: 10.1016/j.purol.2015.01.006. Epub 2015 Feb 3. French.
    Results Reference
    result
    PubMed Identifier
    11412210
    Citation
    Milsom I, Abrams P, Cardozo L, Roberts RG, Thuroff J, Wein AJ. How widespread are the symptoms of an overactive bladder and how are they managed? A population-based prevalence study. BJU Int. 2001 Jun;87(9):760-6. doi: 10.1046/j.1464-410x.2001.02228.x. Erratum In: BJU Int 2001 Nov;88(7):807.
    Results Reference
    result
    PubMed Identifier
    21371240
    Citation
    Coyne KS, Sexton CC, Kopp ZS, Ebel-Bitoun C, Milsom I, Chapple C. The impact of overactive bladder on mental health, work productivity and health-related quality of life in the UK and Sweden: results from EpiLUTS. BJU Int. 2011 Nov;108(9):1459-71. doi: 10.1111/j.1464-410X.2010.10013.x. Epub 2011 Mar 3.
    Results Reference
    result
    PubMed Identifier
    22036776
    Citation
    Denys P, Le Normand L, Ghout I, Costa P, Chartier-Kastler E, Grise P, Hermieu JF, Amarenco G, Karsenty G, Saussine C, Barbot F; VESITOX study group in France. Efficacy and safety of low doses of onabotulinumtoxinA for the treatment of refractory idiopathic overactive bladder: a multicentre, double-blind, randomised, placebo-controlled dose-ranging study. Eur Urol. 2012 Mar;61(3):520-9. doi: 10.1016/j.eururo.2011.10.028. Epub 2011 Oct 25.
    Results Reference
    result
    PubMed Identifier
    10702067
    Citation
    Schurch B, Schmid DM, Stohrer M. Treatment of neurogenic incontinence with botulinum toxin A. N Engl J Med. 2000 Mar 2;342(9):665. doi: 10.1056/NEJM200003023420918. No abstract available.
    Results Reference
    result
    PubMed Identifier
    24472109
    Citation
    Karsenty G, Baverstock R, Carlson K, Diaz DC, Cruz F, Dmochowski R, Fulford S, Giannantoni A, Heesakkers J, Kaufmann A, Peyrat L, Thavaseelan J, Dasgupta P. Technical aspects of botulinum toxin type A injection in the bladder to treat urinary incontinence: reviewing the procedure. Int J Clin Pract. 2014 Jun;68(6):731-42. doi: 10.1111/ijcp.12360. Epub 2014 Jan 29.
    Results Reference
    result
    PubMed Identifier
    24286546
    Citation
    Hermieu JF, Ballanger P, Amarenco G, Chartier-Kastler E, Cosson M, Costa P, Fatton B, Deffieux X, Denys P, Game X, Haab F, Karsenty G, Le Normand L, Ruffion A, Saussine C. [Guidelines for practical usage of botulinum toxin type A (BoNTA) for refractory idiopathic overactive bladder management]. Prog Urol. 2013 Dec;23(17):1457-63. doi: 10.1016/j.purol.2013.10.006. Epub 2013 Nov 7. French.
    Results Reference
    result
    PubMed Identifier
    26599994
    Citation
    Kendrick C, Sliwinski J, Yu Y, Johnson A, Fisher W, Kekecs Z, Elkins G. Hypnosis for Acute Procedural Pain: A Critical Review. Int J Clin Exp Hypn. 2016;64(1):75-115. doi: 10.1080/00207144.2015.1099405.
    Results Reference
    result
    PubMed Identifier
    31410922
    Citation
    Noergaard MW, Hakonsen SJ, Bjerrum M, Pedersen PU. The effectiveness of hypnotic analgesia in the management of procedural pain in minimally invasive procedures: A systematic review and meta-analysis. J Clin Nurs. 2019 Dec;28(23-24):4207-4224. doi: 10.1111/jocn.15025. Epub 2019 Sep 3.
    Results Reference
    result
    PubMed Identifier
    30280915
    Citation
    Gezginci E, Iyigun E, Kibar Y, Bedir S. Three Distraction Methods for Pain Reduction During Cystoscopy: A Randomized Controlled Trial Evaluating the Effects on Pain, Anxiety, and Satisfaction. J Endourol. 2018 Nov;32(11):1078-1084. doi: 10.1089/end.2018.0491.
    Results Reference
    result

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    Effectiveness of HYPNOsis Masks During Botulinum TOXin Injections in Idiopathic Overactive Bladder(HypnoTox)

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