Kannan Priya, Chapple Cathy M, Miller Dawn, Claydon Leica S, Baxter G David
Centre for Health, Activity and Rehabilitation Research, University of Otago, New Zealand.
Centre for Health, Activity and Rehabilitation Research, University of Otago, New Zealand.
Contemp Clin Trials. 2015 May;42:81-9. doi: 10.1016/j.cct.2015.03.010. Epub 2015 Mar 31.
Dysmenorrhea in the absence of pelvic abnormality is termed primary dysmenorrhea (PD). The health burden and social and economic costs of PD are high as it is reported to be the leading cause of recurrent absenteeism from school or work in adolescent girls and young adults. The belief that exercise works for relieving symptoms in women with PD is based on anecdotal evidence and non-experimental studies. There is very limited evidence from randomized controlled trials (RCTs) to support the use of exercise to reduce the intensity of menstrual pain. The objective of this study is to evaluate the effectiveness of exercise to reduce intensity of pain and improve quality of life in women with PD. We describe the study design of a single-blind (assessor), prospective, two-arm RCT, and the participant characteristics of the 70 women recruited in the age-group 18 to 43 years. The primary outcome of the study is pain intensity. The secondary outcomes of the study are quality of life, functional limitation, sleep, global improvement with treatment, and protocol adherence. The outcomes assessments are done at first menstrual period (baseline, Week 0), 2nd menstrual period (Week 4) and at two additional time points (Week 16 and Week 28) during the trial. The results of the study will provide physiotherapists, medical practitioners, and researchers as well as the women who have PD with new insights, knowledge, and evidence about the use of exercise to manage pain in women with PD.
在没有盆腔异常的情况下发生的痛经被称为原发性痛经(PD)。据报道,原发性痛经是青春期女孩和年轻女性反复缺课或旷工的主要原因,因此其健康负担以及社会和经济成本都很高。认为运动有助于缓解原发性痛经女性症状的观点是基于轶事证据和非实验性研究。来自随机对照试验(RCT)的证据非常有限,不足以支持通过运动来减轻经期疼痛的强度。本研究的目的是评估运动对减轻原发性痛经女性疼痛强度和改善生活质量的有效性。我们描述了一项单盲(评估者)、前瞻性、双臂随机对照试验的研究设计,以及招募的70名年龄在18至43岁之间女性的参与者特征。该研究的主要结局是疼痛强度。次要结局包括生活质量、功能受限、睡眠、治疗后的整体改善情况以及方案依从性。结局评估在试验期间的第一个月经期(基线,第0周)、第二个月经期(第4周)以及另外两个时间点(第16周和第28周)进行。该研究结果将为物理治疗师、医生、研究人员以及患有原发性痛经的女性提供有关运动用于管理原发性痛经女性疼痛的新见解、知识和证据。