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Feasibility of Use of Vibrators With Vaginal Dilators for Vaginismus. (Vibrator Therapy and Dilators in Vaginismus) (ViTaDiVa)

Primary Purpose

Vaginismus

Status
Recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
External Vibrator - patient-administered.
Standard care
Sponsored by
Barts & The London NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Vaginismus

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Able and willing to give informed consent (additional measures have to be in place if children, vulnerable adults or adults unable to give consent are included)
  • Female
  • Over the age of 18
  • With symptoms and clinical signs consistent with vaginismus/ vaginismus and vulvodynia.

Exclusion Criteria:

  • Unwilling or unable to give consent
  • Transgender male / on testosterone therapy
  • Inability to understand written and / or verbal English
  • Current dermatological skin conditions requiring active treatment
  • Genital herpes simplex virus symptoms within preceding 3 months
  • Not reporting symptoms of vaginismus, and no evidence of vaginismus on clinical examination.

Sites / Locations

  • Ambrose King Sexual Health CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Vibrator Therapy + dilator/standard therapy

Dilator/standard therapy

Arm Description

Patient will receive standard therapy (initial appointment, referral for womens health physiotherapy or psychosexual counselling as standard, together with vadinal dilators and lidocaine gel) plus an external vibrator.

Patient will receive standard therapy (initial appointment, referral for womens health physiotherapy or psychosexual counselling as standard, together with vadinal dilators and lidocaine gel).

Outcomes

Primary Outcome Measures

Is vibration therapy (through the use of handheld external vibrators on clitoral and vulval area) acceptable to women as part of medical management of vaginismus and vaginismus/vulvodynia, alongside current medical management?
Qualitative questionnaire

Secondary Outcome Measures

Does the use of clitoral/ vulval vibrators help women to progress more easily with the use of vaginal dilators compared to women not using these?
Qualitative questionnaire
Is there any self-reported difference in experiences of pleasure or enjoyment around sexual experiences in the two groups of women as reported by FSDS (Female Sexual Distress Scale) Scores?
Questionnaire - FSDS (above)
Is there any self-reported difference in experiences of pleasure or enjoyment around sexual experiences in the two groups of women as reported by FSFI (Female Sexual Function Index) Scores?
Questionnaire - FSFI (above)

Full Information

First Posted
August 3, 2020
Last Updated
August 7, 2023
Sponsor
Barts & The London NHS Trust
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1. Study Identification

Unique Protocol Identification Number
NCT04635345
Brief Title
Feasibility of Use of Vibrators With Vaginal Dilators for Vaginismus. (Vibrator Therapy and Dilators in Vaginismus)
Acronym
ViTaDiVa
Official Title
A Pilot Study Assessing the Feasibility of Using Clitoral Vibrators to Aid Vaginal Dilator Therapy in Women Presenting to Psychosexual Services With Vaginismus.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 11, 2021 (Actual)
Primary Completion Date
August 2024 (Anticipated)
Study Completion Date
August 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Barts & The London NHS Trust

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The acceptability of vulvar vibration therapy has been evaluated in women with vulvodynia, and found to be acceptable, however has not been assessed in women with a primary complaint of vaginismus. This proposed study looks at the feasibility and acceptability of using clitoral vibration therapy, alongside current therapy, for women with vaginismus. It is likely that many, if not most, of these women will also have an element of vulvodynia. The investigators propose that the use of external clitoral or vulval vibration therapy is likely to be acceptable in most women with vaginismus, based on acceptability of vulvar vibration therapy in women with vulvodynia. It is proposed that vibrator therapy may help women with female sexual dysfunction to use vaginal dilators.
Detailed Description
This is a nonrandomized controlled trial, with the initial cluster of patients receiving standard therapy, and the second cluster receiving standard therapy plus vibrator. Recruitment will be an initial 15 participants who will receive standard therapy, and then another 15 who will receive an external vibrator. This study will take place over approximately 12 months. Enrollment of patients will be from a joint psychosexual clinic led by a medical doctor and a clinical psychologist. Female patients are referred to this clinic by General Practitioners, from within the Sexual Health service, or via Gynaecologists, frequently with complaint of difficulty or pain with penetrative sex. Exclusion criteria will be: patients unable/ unwilling to consent, transgender male or on testosterone therapy, unable to understand written and/or verbal English, current dermtatological skin conditions requiring active treatment, genital herpes simplex virus within 3 months, or not reporting symptoms of vaginismus with no evidence of vaginismus on clinical examination. Trial information will be given at the initial appointment. If the patient wishes to enrol, than an initial baseline questionnaire will be given, and a follow up questionnaire will be filled out by phone contact at 3-4 months afterward the initial consultation at the patients consent.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vaginismus

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Vibrator Therapy + dilator/standard therapy
Arm Type
Experimental
Arm Description
Patient will receive standard therapy (initial appointment, referral for womens health physiotherapy or psychosexual counselling as standard, together with vadinal dilators and lidocaine gel) plus an external vibrator.
Arm Title
Dilator/standard therapy
Arm Type
Active Comparator
Arm Description
Patient will receive standard therapy (initial appointment, referral for womens health physiotherapy or psychosexual counselling as standard, together with vadinal dilators and lidocaine gel).
Intervention Type
Other
Intervention Name(s)
External Vibrator - patient-administered.
Intervention Description
Patient provided with external vibrator for self-use, as well as vaginal dilators.
Intervention Type
Other
Intervention Name(s)
Standard care
Intervention Description
Dilators, lidocaine topical gel, referral to psychotherapy, group therapy or womens health physio if required, self-help resources.
Primary Outcome Measure Information:
Title
Is vibration therapy (through the use of handheld external vibrators on clitoral and vulval area) acceptable to women as part of medical management of vaginismus and vaginismus/vulvodynia, alongside current medical management?
Description
Qualitative questionnaire
Time Frame
12-18 months
Secondary Outcome Measure Information:
Title
Does the use of clitoral/ vulval vibrators help women to progress more easily with the use of vaginal dilators compared to women not using these?
Description
Qualitative questionnaire
Time Frame
12-24 months
Title
Is there any self-reported difference in experiences of pleasure or enjoyment around sexual experiences in the two groups of women as reported by FSDS (Female Sexual Distress Scale) Scores?
Description
Questionnaire - FSDS (above)
Time Frame
12-24 months
Title
Is there any self-reported difference in experiences of pleasure or enjoyment around sexual experiences in the two groups of women as reported by FSFI (Female Sexual Function Index) Scores?
Description
Questionnaire - FSFI (above)
Time Frame
12-24 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Able and willing to give informed consent (additional measures have to be in place if children, vulnerable adults or adults unable to give consent are included) Female Over the age of 18 With symptoms and clinical signs consistent with vaginismus/ vaginismus and vulvodynia. Exclusion Criteria: Unwilling or unable to give consent Transgender male / on testosterone therapy Inability to understand written and / or verbal English Current dermatological skin conditions requiring active treatment Genital herpes simplex virus symptoms within preceding 3 months Not reporting symptoms of vaginismus, and no evidence of vaginismus on clinical examination.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jessica Gaddie, MbCHb, BSc
Phone
0207 377 7315
Email
j.gaddie1@nhs.net
First Name & Middle Initial & Last Name or Official Title & Degree
Jill Zelin
Email
jill.zelin@nhs.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jess Gaddie
Organizational Affiliation
Barts & The London NHS Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ambrose King Sexual Health Centre
City
London
ZIP/Postal Code
E1 2BB
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jessica Gaddie, MBChB
Email
j.gaddie1@nhs.net

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Feasibility of Use of Vibrators With Vaginal Dilators for Vaginismus. (Vibrator Therapy and Dilators in Vaginismus)

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