首页> 外文期刊>Contemporary clinical trials >Menstrual pain and quality of life in women with primary dysmenorrhea: Rationale, design, and interventions of a randomized controlled trial of effects of a treadmill-based exercise intervention
【24h】

Menstrual pain and quality of life in women with primary dysmenorrhea: Rationale, design, and interventions of a randomized controlled trial of effects of a treadmill-based exercise intervention

机译:原发性痛经女性的月经疼痛和生活质量:基于跑步机的运动干预效果的随机对照试验的原理,设计和干预

获取原文
获取原文并翻译 | 示例
           

摘要

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.
机译:没有骨盆异常的痛经被称为原发性痛经(PD)。帕金森氏病的健康负担以及社会和经济成本很高,因为据报道,帕金森氏病是少女和年轻人中因学校或工作反复缺勤的主要原因。认为锻炼能减轻PD患者的症状的信念是基于轶事证据和非实验研究。随机对照试验(RCT)所提供的证据表明,使用运动减轻月经痛的程度非常有限。这项研究的目的是评估运动对减轻PD患者的疼痛强度和改善生活质量的有效性。我们描述了单盲(评估者),前瞻性,两臂RCT的研究设计,以及年龄在18至43岁之间的70名女性的参与者特征。该研究的主要结果是疼痛强度。该研究的次要结果是生活质量,功能受限,睡眠,治疗的整体改善和方案依从性。在试验期间,在第一月经期(基线,第0周),第二月经期(第4周)和其他两个时间点(第16周和第28周)进行结果评估。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号