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临床试验/NCT02938936
NCT02938936已完成不适用

Waiting Time. Wasting Time: A Randomized Control Trial to Investigate the Health Impacts of Improving the Quality of Antenatal Care in Mozambique

Harvard School of Public Health (HSPH)0 个研究点目标入组 597 人开始时间: 2016年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
597
主要终点
Change in percent of women completing at least 4 prenatal care visits before and after intervention

研究概览

简要总结

Our study's principle purpose is to determine whether decreasing waiting time before being seen for antenatal care increases demand for and use of antenatal care services in Mozambique.

详细描述

This protocol describes a pilot study that will test the impact of a scheduling intervention intended to reduce waiting times for antenatal care. The study will include one intervention health clinic and one control clinic in Maputo, Mozambique. In the intervention facility women attending antenatal care will be informed that if they return at their scheduled date and time they will be seen within one hour by clinic staff rather than having to wait for an indefinite amount of time before being seen for care. Appointment cards will be clipped into ANC cards, which collect routine health data and are kept by women at the end of their ANC visit. Health facility staff will be trained to identify women who return at their scheduled time and to manage patient flow such that scheduled women are received quickly. After the start date of the intervention, all women attending ANC at the health facility will be provided a scheduled return date and time window. Baseline and endline exit interview surveys will be conducted in both intervention and control facilities to compare changes in waiting time, number of ANC visits, and provider satisfaction over the course the study period between clinics.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Inclusion criteria for individual study participants enrolled after delivery:
  • Women who delivered at the health facility during the weeks of recruitment
  • Inclusion criteria for women whose waiting time is measured:
  • Women at the health facility to seek care for antenatal care or another reproductive health service (anticipate total enrollment of 800 women)
  • Inclusion criteria for the health care provider survey is that the provider
  • Have worked in the health facility for at least 6 months
  • The health care worker provides ANC as part of their routine duties (anticipate total enrollment of 4 health care workers)

排除标准

  • Exclusion criteria for individual study participants enrolled after delivery:
  • Women under 18 years of age will be excluded
  • Women whose babies die during labor or childbirth from the delivery exit interviews
  • There are no exclusion criteria for the sample of women whose waiting time will be measured There are no exclusion criteria for the health care provider survey

研究组 & 干预措施

Scheduling Intervention

Experimental

Pre-natal visit scheduling

干预措施: Pre-natal visit scheduling (Other)

Control

No Intervention

结局指标

主要结局

Change in percent of women completing at least 4 prenatal care visits before and after intervention

时间窗: During most recent pregnancy, as reported in an exit survey conducted at discharge from delivery at baseline and six months after the start of the scheduling intervention

Change in average waiting time before being seen for prenatal care before and after intervention

时间窗: Measured for 4 weeks at baseline before the start of the intervention, and for 4 weeks, 3 months after the start of the intervention

次要结局

  • Change in proportion of key ANC services respondent reports receiving at most recent prenatal care visit, 9 possible services measured in exit survey at discharge from delivery.(Measured at baseline and 6 months after the start of the intervention)
  • Change in nurses satisfaction with their job (1-5 scale)(Measured before the start of the intervention, and 6 months after the start of the intervention)

研究者

发起方
Harvard School of Public Health (HSPH)
申办方类型
Other
责任方
Principal Investigator
主要研究者

Margaret McConnell

Assistant Professor of Global Health Economics

Harvard School of Public Health (HSPH)

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