Hypnotic Intervention for Women With Chronic Pelvic Pain
CompletedNot applicableNCT04851626
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
Objective: To establish whether the pilot online hypnosis design was well received by women with persistent pelvic pain and worthy of a full randomised control trial To establish whether hypnosis improves mental health outcomes, including anxiety, depression, life impact and catastrophizing, in women with chronic pelvic pain conditions.
Study details
- Official title
- Hypnotic Intervention for Women With Chronic Pelvic Pain: a Pilot Randomised Control Trial
- Conditions
- Chronic Pain
- Pelvic Pain
- Psychological
- Hypnosis, Animal
- Interventions
- Other: Hypnotic intervention for persistent pelvic pain.
- Other: Control group persistent pelvic pain no intervention.
- Sponsor
- University of South Australia
- Start date
- 2020-11-02
- Primary completion
- 2020-12-21
- Sex
- Female
- Age range
- from 18 Years to 100 Years
- Results posted
- No results posted in this snapshot
- Countries
- Australia
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Meets criteria for persistent pelvic pain. Having experienced pain in the pelvic region below the umbilicus for over three months either beyond the healing time of a pathology or injury or without a diagnosed cause. * Must be biologically female. * Must be over the age of 18 years old. Exclusion Criteria: * Must not have a previously diagnosed or current mental health disorder involving dissociative states. Examples include diagnosed or current symptoms of Bipolar Type 1 or 2, psychotic disorders, untreated Post-Traumatic Stress Disorder. * Must not reported current plan or intent to commit suicide.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04851626