Improving Maternal and Child Health in India: Evaluating Demand and Supply Side Strategies (IMATCHINE) (IMATCHINE)

Improving Maternal and Child Health in India: Evaluating Demand and Supply Side Strategies

The study evaluates the impact of a new conditional cash transfer (CCT) program (Thayi Bhagya Yojana) to promote child birth in obstetric facilities in the state of Karnataka, India in order to determine its policy value and to guide efforts to improve maternal and infant health outcomes nationally. In addition, the study includes a large randomized evaluation of performance-based incentive payments to providers to improve quality of medical care provided during delivery and actual health improvement in the providers' patient populations and their catchment areas.

Study Overview

• Status: Completed
• Conditions: Sepsis; Obstetric Labor Complications; Pre-eclampsia; Neonatal Mortality; Post-partum Hemorrhage
• Intervention / Treatment: Other: Experimental: Treatment 1; Other: Experimental: Treatment 2

Detailed Description

The evaluation study will first provide new evidence on the effectiveness of demand-side strategies to increase institutional deliveries and improve childbirth outcomes. Second, the study will analyze one of the first implementations of direct rewards to providers for health improvement in a developing country. Third, the study will provide critical new insight into dynamics between demand and supply-side incentives in improving population health outcomes as either complements or substitutes.

The study uses household survey to collect data from mothers on socio-economic, human capital, quality of life variables (including below poverty line [BPL] index components) and as well as information about deliveries, fertility histories, morbidity and mortality (for mothers, infants, and children), birth related complications, health service use and spending. Additionally, provider surveys will collect data on infrastructure, staffing, provider qualifications, provider knowledge and process measures of provider performance.

• Study Type: Interventional
• Enrollment (Anticipated): 14990
• Phase: Not Applicable

Contacts and Locations

Study Locations

• India
  • Karnataka
    • Bangalore, Karnataka, India
      • Imatchine

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Households with new mothers (one to three weeks after childbirth)
• Rural private sector maternity care providers who are listed on the Karnataka government's legitimate provider list.

Exclusion Criteria:

• Households without children
• Households where mothers gave birth > 3 weeks ago
• Public sector maternity care providers
• Private sector maternity care providers serving in towns with large public providers such as Community Health Centers (CHCs)

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Health Services Research
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

4

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
No Intervention: Mothers at endline; Data collected on new mothers (up to three weeks after childbirth) in 180 clusters with 100 mothers in each cluster at endline.
Experimental: Treatment 1; Data collected on new mothers (up to three weeks after childbirth) and on providers with incentives for clinical improvements in quality of maternity care in the providers' patient populations and the catchment areas served by the providers.	Other: Experimental: Treatment 1; Physicians will receive financial incentives for improving the quality of obstetric and neonatal care provided to mothers and newborns as reported by mothers during household interviews.
Experimental: Treatment 2; Data collected on new mothers (up to three weeks after childbirth) and on providers with incentives for improvement in maternal and infant health outcomes in the providers' patient populations and in the catchment areas served by the providers.	Other: Experimental: Treatment 2; Physicians will receive financial incentives for improving maternal and neonatal health outcomes as reported by mothers during household interviews.
No Intervention: Control; Data collected on new mothers (up to three weeks after childbirth) and providers with no incentives

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Increase institutional deliveries and improve maternal and infant health outcomes in the population.	Rates of deliveries in hospitals and maternal health complications such as obstetric fistulas, post-partum hemorrhage, sepsis, as well as neonatal outcomes.	1 Year

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Effectiveness of financial incentives to maternity care private providers for improvements in the clinical quality of services in the providers' patient populations and the catchment areas they serve.	Indicators of quality of services include monitoring of the fetal heartbeat, active management of labor, and monitoring of cervical dilation and effacement.	1 Year
Effectiveness of financial incentives to maternity care private providers for improvements in maternal and infant health outcomes in the providers' patient populations and the catchment areas they serve.	Indicators of improvements in maternal and neonatal health outcomes include reduced incidence of maternal morbidity outcomes such as obstetric fistulas, excessive post partum bleeding, sepsis, hospital readmission, as well as neonatal outcomes.	1 Year

Collaborators and Investigators

• Sponsor: Duke University
• Collaborators: Stanford University; Department for International Development, United Kingdom; International Initiative for Impact Evaluation; Sambodhi Research and Communication Pvt., Ltd.
• Investigators: Principal Investigator: Manoj Mohanan, PhD, MPH, Duke University

Study record dates

Study Major Dates

• Study Start: August 1, 2012
• Primary Completion (Actual): December 1, 2014
• Study Completion (Actual): November 1, 2015

Study Registration Dates

• First Submitted: November 8, 2011
• First Submitted That Met QC Criteria: November 28, 2011
• First Posted (Estimate): November 29, 2011

Study Record Updates

• Last Update Posted (Estimate): December 16, 2015
• Last Update Submitted That Met QC Criteria: December 14, 2015
• Last Verified: December 1, 2015

More Information

Terms related to this study

• Keywords: Randomized Control Trial; Maternal Health; Infant Health; Institutional Deliveries; Private Medical Providers; Provider Incentives
• Additional Relevant MeSH Terms: Pathologic Processes; Pregnancy Complications; Puerperal Disorders; Hypertension, Pregnancy-Induced; Uterine Hemorrhage; Hemorrhage; Obstetric Labor Complications; Eclampsia; Pre-Eclampsia; Postpartum Hemorrhage
• Other Study ID Numbers: Pro00031046