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临床试验/ACTRN12619000316101
ACTRN12619000316101已完成未知

Effect of physiotherapy-led group therapy on pain reporting and quality of life in women with chronic pelvic pain

Women's and Children's Hospital0 个研究点目标入组 90 人开始时间: 2019年2月28日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
90

研究概览

简要总结

Female persistent pelvic pain (PPP) is a complex and often debilitating condition requiring multi-disciplinary input for effective management. Increasing recognition of the important role of Physiotherapy in treating this patient cohort led to referral numbers to Women’s Physiotherapy at the Women’s and Children’s Hospital (WCH) increasing in an unsustainable way for the individualised care approach in place. A more efficient and coordinated approach was required to ensure women with PPP were able to access the care they needed in a timely manner, while maintaining the positive clinical outcomes achieved through a traditional care pathway. This project tested the impact of implementing best practice chronic pain management strategies, proven effective with other patient groups such as chronic back pain sufferers, on clinical outcomes and consumer satisfaction for women referred with PPP, when compared to the usual model of care. Eligible women were recruited into one of three treatment arms; 1) individual consultations (usual care), 2) an introductory group pain science education session followed by individual care and 3) an introductory group pain science education session followed by weekly group therapy sessions and individual care. The study demonstrated the benefit of Physiotherapy in the management of PPP, with statistically significant improvements in all clinical outcome measures and highly positive consumer feedback observed across all treatment arms. It demonstrated that the addition of a group pain science education session as a precursor to individual consultation and care (treatment arm 2) results in improved clinical outcomes (with respect to self-reported impact of pelvic pain on function and participation), when compared to those receiving individual consultation alone (treatment arm 1). While the addition of an 8-week group exercise program (treatment arm 3) demonstrated statistically significant improvements for those in the group, there was no significant added benefit when compared women assigned to treatment arm 2.

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
15 Years 至 o limit(—)
性别
Female

入选标准

  • Pelvic pain that has been present for 6 months or more that has been medically investigated, with or without confirmed or suspected endometriosis

排除标准

  • a) women from non-English speaking backgrounds requiring interpreting assistance,
  • b) women with known intellectual disability,
  • c) women who have previously accessed Physiotherapy intervention for CPP,
  • d) women with known presence of active, major mental disorder (e.g. psychotic disorder, clear suicide risk) and/or significant mental health symptoms precluding group participation,
  • e) women with an acute physical condition or illness exists which is currently being treated in a manner which would preclude adequate participation in the program,
  • f) women who have not had the source of their persistent pain adequately investigated medically.

研究者

发起方
Women's and Children's Hospital

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