Pelvic floor muscle training versus watchful waiting or pessary treatment for pelvic organ prolapse (POPPS): Design and participant baseline characteristics of two parallel pragmatic randomized controlled trials in primary care

被引:25
作者
Wiegersma, Marian [1 ]
Panman, Chantal M. C. R. [1 ]
Kollen, Boudewijn J. [1 ]
Vermeulen, Karin M. [2 ]
Schram, Aaltje J. [3 ]
Messelink, Embert J. [4 ]
Berger, Marjolein Y. [1 ]
Lisman-Van Leeuwen, Yvonne [1 ]
Dekker, Janny H. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Gen Practice, NL-9700 AD Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, NL-9700 AD Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Gynecol, NL-9700 AD Groningen, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Urol, NL-9700 AD Groningen, Netherlands
关键词
Pelvic organ prolapse; Pelvic floor muscle training; Pessaries; Watchful waiting; Primary health care; Pragmatic randomized controlled trial; QUALITY-OF-LIFE; SHORT-FORM; TERMINOLOGY; STANDARDIZATION; INCONTINENCE; DISORDERS; SYMPTOMS;
D O I
10.1016/j.maturitas.2013.10.014
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Pelvic floor muscle training (PFMT) and pessaries are commonly used in the conservative treatment of pelvic organ prolapse (POP). Because there is a lack of evidence regarding the optimal choice between these two interventions, we designed the "Pelvic Organ prolapse in primary care: effects of Pelvic floor muscle training and Pessary treatment Study" (POPPS). POPPS consists of two parallel open label randomized controlled trials performed in primary care, in women aged >= 55 years, recruited through a postal questionnaire. In POPPS trial 1, women with mild POP receive either PFMT or watchful waiting. In POPPS trial 2, women with advanced POP receive either PFMT or pessary treatment. Patient recruitment started in 2009 and was finished in December 2012. Primary outcome of both POPPS trials is improvement in POP-related symptoms. Secondary outcomes are quality of life, sexual function, POP-Q stage, pelvic floor muscle function, post-void residual volume, patients' perception of improvement, and costs. All outcomes are measured 3, 12, and 24 months after the start of treatment. Cost-effectiveness will be calculated based on societal costs, using the PFDI-20 and the EQ-5D as outcomes. In this paper the POPPS design, the encountered challenges and our solutions, and participant baseline characteristics are presented. For both trials the target numbers of patients in each treatment group are achieved, giving this study sufficient power to lead to promising results. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:168 / 173
页数:6
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