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Waiting Time. Wasting Time

Not Applicable
Completed
Conditions
Pregnancy
Interventions
Other: Pre-natal visit scheduling
Registration Number
NCT02938936
Lead Sponsor
Harvard School of Public Health (HSPH)
Brief Summary

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.

Detailed Description

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.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
597
Inclusion Criteria

Inclusion criteria for individual study participants enrolled after delivery:

  1. Women who delivered at the health facility during the weeks of recruitment

Inclusion criteria for women whose waiting time is measured:

  1. 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

  1. Have worked in the health facility for at least 6 months
  2. The health care worker provides ANC as part of their routine duties (anticipate total enrollment of 4 health care workers)
Exclusion Criteria

Exclusion criteria for individual study participants enrolled after delivery:

  1. Women under 18 years of age will be excluded
  2. 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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Scheduling InterventionPre-natal visit schedulingPre-natal visit scheduling
Primary Outcome Measures
NameTimeMethod
Change in percent of women completing at least 4 prenatal care visits before and after interventionDuring 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 interventionMeasured for 4 weeks at baseline before the start of the intervention, and for 4 weeks, 3 months after the start of the intervention
Secondary Outcome Measures
NameTimeMethod
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

9 key services include:

* IPTP dose provided, measured by self-report

* Delivery plan discussed, measured by self-report

* Hemoglobin test measured by patient report of having had their blood drawn

* Recommendations for family planning and breast feeding provided, measured by self-report

* Detection of breech measured by report of the provider palpating the tummy

* Blood pressure

* Measurement of uterine height

* Urine test

* Recommendation for what to do in emergencies

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
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