...
首页> 外文期刊>Revista Latino-Americana de Enfermagem >Comparison among the efficacy of interventions for the return rate to receive the pap test report: randomized controlled clinical trial 1
【24h】

Comparison among the efficacy of interventions for the return rate to receive the pap test report: randomized controlled clinical trial 1

机译:接受宫颈涂片检查报告的回报率干预措施的功效比较:随机对照临床试验1

获取原文
           

摘要

ABSTRACT Objective: to test the effects of a behavioral, an educative and a comparative intervention on women's adherence to the return appointment to receive the pap test report. Methods: randomized controlled clinical trial at a Primary Health Care Service, involving three groups: EG (educative session and test demonstration), BG (recall ribbon) and standard intervention (card containing the return appointment - graphical reminder), called comparative group here (CG). To select the sample, the following was established: having started sexual activity and undergoing the pap smear during the study, resulting in 775 women. Results: among the 775 women, 585 (75.5%) returned to receive the test result within 65 days. The educative group presented the highest return rate (EG=82%/CG=77%/BG=66%), statistically significant only when compared to the behavioral group (p=0.000). The educative group obtained the smallest interval (p<0.05) concerning the mean number of days of return to receive the test result (EG:M=43days/BG:M=47.5days/CG:M=44.8 days). Conclusion: the educative group reached higher return rates and the women returned earlier, but the behavioral intervention showed to be the least effective. Brazilian Clinical Trial Register: RBR-93ykhs.
机译:摘要目的:测试行为,教育和比较干预措施对妇女遵守回国任命接受子宫颈抹片检查报告的影响。方法:在初级卫生保健服务机构进行的随机对照临床试验,分为三组:EG(教育会议和测试演示),BG(召回功能区)和标准干预措施(包含返回预约的图形提醒),在此处称为比较组( CG)。为了选择样本,确定了以下内容:在研究期间已开始性活动并进行了子宫颈抹片检查,结果有775名妇女。结果:在775名女性中,有585名(75.5%)在65天内返回接受测试结果。教育组的回报率最高(EG = 82%/ CG = 77%/ BG = 66%),仅与行为组相比有统计学意义(p = 0.000)。对于接受测试结果的平均返回天数,教育组获得的最小间隔(p <0.05)(EG:M = 43天/BG:M=47.5天/CG:M=44.8天)。结论:教育组的返乡率较高,妇女返乡较早,但行为干预效果最差。巴西临床试验注册簿:RBR-93ykhs。

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