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Primary Care Provider Supply and Patient Outcomes

Estimating the Returns to Provider Human Capital

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03131193
Enrollment
10852
Registered
2017-04-27
Start date
2017-03-20
Completion date
2022-06-30
Last updated
2022-10-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Services Accessibility, Health Behavior, Health Care Quality, Access, and Evaluation

Brief summary

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.

Detailed description

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.

Interventions

Study primary health centers will be staffed with an additional physician

OTHERMid-level provider

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

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

Sponsors

RAND
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Clinic attendance6-12 months after enrollmentUtilization of health services will be measured using a questionnaire
Self-reported health6-12 months after enrollmentSelf-reported health status will be measured using a questionnaire

Secondary

MeasureTime frameDescription
Mortality6-12 months after enrollmentChild mortality will be measured using a questionnaire
Quality of care6-12 months after enrollmentProcess quality based on adherence to clinical protocols will be measured via direct observation (observer will complete a standardized checklist)
Child weight12 months after enrollmentChild weight in kg will be measured using a weighing scale
Child height12 months after enrollmentChild height in cm will be measured using a measuring board or stadiometer as appropriate

Countries

Nigeria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026