Virtual Mindfulness for the Management of Endometriosis Pelvic Pain.
NCT ID: NCT05554497
Last Updated: 2023-12-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
15 participants
INTERVENTIONAL
2021-02-01
2023-01-13
Brief Summary
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The objective of this pilot project is to assess the effectiveness of virtual mindfulness-based workshops to improve quality of life and pain in patients with endometriosis. The information from the workshops will then be used to create free online resources for patients to learn mindfulness-based approaches to manage endometriosis-related pelvic pain to reduce the financial and geographical barriers to access. Better access to mindfulness-based endometriosis management will enhance the treatment options for people suffering from this condition.
Detailed Description
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A registered social worker with knowledge of gynecology clinic practice will create and run the virtual mindfulness workshops based on a standard mindfulness-based stress reduction curriculum. She will receive additional training in teaching mindfulness prior to the start of the study. The workshops will run weekly for eight-weeks over the Zoom platform. The sessions will last 2.5 hours and be held in the evening to ensure those with daytime commitments can participate.
For this pilot project a before and after study design will be employed. Participants will complete questionnaires before and after participation in the eight-week mindfulness workshop. Follow up questionnaires will be completed six and twelve months after completion of the workshop. The primary outcome for this study is an improvement in quality-of-life measures. Secondary outcomes are decrease in pain intensity, reduction in psychological stress, improvement in sexual function, reduction in quantity of pain modifiers used and reduction in opiate pain medication use. These main outcomes will be measured using a previously validated tool, The Endometriosis Health Profile Questionnaire (EHP-30).29 Additional tools to assess baseline demographics, barriers to accessing mindfulness and pain medication use have been created for this study. This project has been submitted to the St. Michael's Hospital research ethics board for approval.
Upon completion of the curriculum participants will be invited to a focus group to provide qualitative feedback on their experiences with mindfulness-based stress reduction, personal barriers to accessing this treatment, how it contributed to their overall treatment plan and types of activities they found mindfulness most useful for. This data will be coded by two members of the research team to look for themes and potential areas for improvements or change before proceeding with future workshops. It will also be used to inform future knowledge translation projects.
An initial 15 participants will be recruited to the study from the gynaecology clinics at St. Michael's hospital. This is a maximum group size suggested for an effective mindfulness workshop. The goal of this small group is to determine the feasibility and effectiveness of mindfulness-based therapy for endometriosis-related pelvic pain delivered in a virtual platform prior to completing a larger study.
Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Mindfulness training
8 week virtual mindfulness-based stress reduction curriculum. Weekly 2.5 hour sessions over zoom.
Mindfulness-based stress reduction curriculum
Standard 8-week mindfulness-based stress reduction curriculum
Interventions
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Mindfulness-based stress reduction curriculum
Standard 8-week mindfulness-based stress reduction curriculum
Eligibility Criteria
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Inclusion Criteria
* Have been symptomatic for six months or greater;
* Clinical or surgical diagnosis of endometriosis (must have at least one of the following):
i)Documented Clinical Diagnosis of endometriosis based on symptoms
ii)Previous endometriosis surgery confirmed by histopathology
iii)Imaging suggestive of endometriosis (ultrasound or MRI)
iv)Receiving standard medical treatment for endometriosis including combined oral contraceptives, progestin, GnRH agonists, GnRH antagonist.
Exclusion Criteria
* Vulvar pain diagnosis including vulvodynia, vaginismus
* Changes to current medical treatment or surgical intervention for endometriosis during the workshop period (8 weeks) which will be reviewed at the start of each workshop session;
* Inability to attend at least 6 out of the 8-sessions;
* Inability to complete the survey package before and after the total 8-session period;
* Prior mindfulness-based workshop participation or training;
* Currently practicing mindfulness meditation.
* No internet access and microphone access: for the use of the zoom virtual platform and to enable participation in the workshops.
* Non-English speaking.
* Unable to consent.
18 Years
45 Years
FEMALE
Yes
Sponsors
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Unity Health Toronto
OTHER
Responsible Party
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Locations
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Unity Health Toronto - St. Michael's Hospital
Toronto, Ontario, Canada
Countries
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Other Identifiers
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20-285C
Identifier Type: -
Identifier Source: org_study_id