Status:
COMPLETED
Program to Overcome Pelvic Pain With Yoga
Lead Sponsor:
University of California, San Francisco
Collaborating Sponsors:
Patty Brisben Foundation For Women's Sexual Health
Conditions:
Pelvic Pain
Eligibility:
FEMALE
21+ years
Phase:
NA
Brief Summary
The POPPY Study is a pilot of an Iyengar-based, therapeutic yoga program, used to treat pelvic or genital pain, in up to 16 women. Women aged 21 years and older who report persistent or recurrent pelv...
Eligibility Criteria
Inclusion
- Women aged 21 years or older who report difficulties with pelvic or genital pain for at least 6 months
- Report that their chronic pelvic or genital pain has had an adverse effect on their interest in or ability to enjoy sexual activity
- Report an eligible average daily pain intensity score after completion of a Daily Pain Log for one week prior to baseline
- Have an established primary care or gynecologic healthcare provider (to facilitate medical follow-up of any health issues detected incidentally in the study or adverse events that develop during the study)
- Report prior clinical evaluation of their pelvic or genital pain by a health care professional including at least a superficial pelvic exam
- Willing to refrain from initiating other new clinical treatments that may affect their pelvic or genital pain during the study period (6 weeks)
Exclusion
- Participation in organized yoga classes in the past 1 month, or any prior yoga therapy directed specifically at pelvic or genital pain (regardless of timing)
- Currently pregnant (by self-report or screening test), pregnant within the past 6 months, planning pregnancy during the study, or unwilling to use contraception (if not postmenopausal) during the study
- Diagnosed with an alternate cause of pain that is unlikely to respond to yoga and requires another treatment modality, such as pelvic infection or a gynecologic dermatosis
- Surgery to the vulva, vagina, cervix, or pelvic organs within 6 months of screening, or any prior history of cancer or irradiation to these structures
- Initiation of or dose escalation of pharmacologic agents that may affect pelvic or genital pain in the past 1 month (e.g., antidepressants, anticonvulsants, anxiolytics)-women on stable dose for \>1 month are eligible
- Use of formal psychological therapies specifically for pelvic or genital pain (e.g., systematic desensitization, sex therapy, cognitive therapy, relaxation therapy) within 1 month of screening
- Use of formal behavioral therapies for pelvic or genital pain (e.g., pelvic floor rehabilitation or biofeedback performed by a certified healthcare practitioner) within 1 month of screening
- Unable to walk up a flight of stairs or at least 2 blocks on level ground (i.e., functional capacity \< 4 METs), or unable to get up from a supine to a standing position without assistance in \<10 seconds
- Currently involved in a malpractice suit or other litigation specifically related to pelvic or genital pain
- Participation in another interventional study that might interfere with or confound study procedures, inability to sign an informed consent or fill out questionnaires, or conflict with available yoga class dates
Key Trial Info
Start Date :
October 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2016
Estimated Enrollment :
16 Patients enrolled
Trial Details
Trial ID
NCT02261740
Start Date
October 1 2014
End Date
June 1 2016
Last Update
October 4 2016
Active Locations (1)
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1
University of California, San Francisco
San Francisco, California, United States, 94115