Skip to main content
OpenTrials
Completed

NCT Number: NCT03131193

Primary Care Provider Supply and Patient Outcomes

The evidence on how primary care provider supply and skill relates to patient outcomes is limited and inconclusive. The issue of skill is a particularly important one in low-income countries where the shortage of skilled medical professionals has led to greater use of the task-shifting model in which medical tasks are redistributed from highly skilled health workers to mid-level providers who receive less training. In this large-scale cluster-randomized trial, the investigators randomly select primary health care facilities to receive a highly skilled provider (a doctor), a mid-level health provider, or no additional providers (the control group). The investigators study the effect of this intervention on patient outcomes. Embedded within this trial is another experimental intervention in which pregnant women residing in communities served by the primary health care facilities are assigned to receive a cash transfer conditional on using antenatal, delivery and postnatal care. The investigators study the effect of the cash transfer on health care utilization and on maternal and infant outcomes.

Completed

Looking for future studies?

Notify Me

Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Aminu Kano Teaching Hospital

Kano, Nigeria

About this study

180 primary health care facilities in Nigeria are participating in this study. In one arm of this trial, 60 of the participating facilities are randomly assigned a physician (in addition to existing clinic staff); in a second arm, 60 facilities are randomly assigned an additional mid-level provider (of similar training to existing providers); and the third arm consists of facilities that receive no additional providers (the control group). Assigned providers will practice in those facilities for approximately one year. Stratifying by treatment arm, the investigators further randomize 10-15 enumeration areas within each facility catchment (service) area to either a Conditional Cash Transfer (CCT) arm or to a control arm. The cash transfer is intended for currently pregnant women in those enumeration areas and is conditioned upon attending four antenatal care visits, giving birth in the facility, and attending at least one postnatal visit.

To measure the effects of the interventions the investigators randomly sample 15 households in each facility catchment area and enroll all currently pregnant women within the study enumeration areas. Women at an advanced stage of pregnancy - third trimester - are excluded because such women will not be exposed to the intervention for the majority of their pregnancy. All household members are interviewed at baseline, midline (6 months later) and endline (12 months later) to collect information about health-seeking behavior and health status. Pregnant women are also interviewed at baseline and approximately 1-3 months after birth to collect information about health care utilization and birth outcomes. Additionally the investigators collect data from the participating health facilities and providers. Using a combination of provider surveys, clinical vignettes, direct clinical observation, and patient exit interviews the investigators examine the effects of the intervention on service delivery and quality.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for Households:

  • Resident in a community served by the study PHC

Exclusion criteria

for Households: none

Inclusion criteria

for Women:

  • Resident in a community served by the study PHC
  • Must be in 1st or 2nd trimester of pregnancy

Exclusion criteria

for Women:

  • 3rd trimester of pregnancy

Treatment and study plan

Physician

Other

Study primary health centers will be staffed with an additional physician

Mid-level provider

Other

Study primary health centers will be staffed with an additional mid-level provider

Conditional cash transfer

Behavioral

Study participants (who are pregnant women) will receive a cash transfer conditional upon: registering for and attending antenatal care in the study clinic, giving birth in the study clinic and completing a postnatal visit with the new infant

Primary outcomes

  1. Clinic attendance

    Time frame: 6-12 months after enrollment

    Utilization of health services will be measured using a questionnaire

  2. Self-reported health

    Time frame: 6-12 months after enrollment

    Self-reported health status will be measured using a questionnaire

Secondary outcomes

  1. Mortality

    Time frame: 6-12 months after enrollment

    Child mortality will be measured using a questionnaire

  2. Quality of care

    Time frame: 6-12 months after enrollment

    Process quality based on adherence to clinical protocols will be measured via direct observation (observer will complete a standardized checklist)

  3. Child weight

    Time frame: 12 months after enrollment

    Child weight in kg will be measured using a weighing scale

  4. Child height

    Time frame: 12 months after enrollment

    Child height in cm will be measured using a measuring board or stadiometer as appropriate

Sponsors and collaborators

Lead sponsor

RAND

Other

Registry information

Official study title

Estimating the Returns to Provider Human Capital

Important dates

Study start
2017
Primary completion
2018
Study completion
2022
First posted
Apr 27, 2017
Registry last updated
Oct 21, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.