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Clinical Trials/NCT01003587
NCT01003587UnknownNot Applicable

Improving Use of Evidence in Policy: District Evaluation Study on Health

Unity Health Toronto4 sites in 2 countries594 target enrollmentStarted: July 2009Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
594
Locations
4
Primary Endpoint
Percentage facility-based births for the last child since 2007

Study Overview

Brief Summary

The purpose of this study is to assess the impact of disseminating information on comparative performance, along with actionable messages on how to improve health outcomes, to district-level decision-makers in India using a randomized, controlled design. This information should improve prioritization of health services by district health officers, budget allocation for health, and implementation of priority health services at the district level.

Detailed Description

Use of evidence in policy is uneven, leading to frequent waste of resources. However, the best way to promote evidence uptake in policy formulation and implementation is unclear. Information on disease control priorities based on India's disease burden and health system capacity has been produced to help focus government efforts during a period of increased spending and decentralization.

This study tests the impact of sending information on comparative performance (using district report cards) and actionable messages (on how to reduce disease burden) to district-level decision-makers on uptake of disease control priority recommendations in India. Using a cluster-randomized design, districts will be randomized to receive either the mailed information package or no intervention. The sample includes all 594 Indian districts in existence in 2001. The intervention will target key district level decision-makers: parliamentarians (Members of Parliament, Members of Legislative Assembly), bureaucrats (District Collectors), technocrats (District Health Officers), and local government officials (Zilla Parishad CEOs).

Study outcome data will be collected using sequential national surveys of health service availability and utilization, including relevant rounds of the District Level Health and Facility Surveys and the Annual Health Surveys. This study tests an inexpensive, pragmatic strategy on a large scale and will provide information on effective methods of knowledge translation to policy-makers.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

District health information package

Experimental

Intervention: District health information package (Behavioral)

No Intervention

No Intervention

Outcomes

Primary Outcomes

Percentage facility-based births for the last child since 2007

Time Frame: Five years

Percentage children 12-23 months vaccinated against measles

Time Frame: Five years

Percentage children <3 yrs with diarrhea in past 2 weeks given oral rehydration solution

Time Frame: Five years

Secondary Outcomes

  • Percentage women given advice on breastfeeding and newborn thermal care during antenatal care(Five years)
  • Percentage last child >3 yrs breast fed within 1 hr of birth(Five years)
  • Percentage community health centres with at least 1 surgeon or ob/gyn(Five years)
  • Percentage public health centres with reagents, light microscope and lab technician for malaria blood smear(Five years)
  • Percentage subcenters with oral rehydration solution available on day of survey and no stockouts for more than 10 days in last month(Five years)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (4)

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