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Strengthen the Evidence for Maternal and Child Health Programs

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Displaying records 1 through 4 (4 total).

ESM 15.1 Percent of families receiving family-to-family support who report increased confidence in navigating care for their child (Minnesota)

Measure Status: Active

Evidence Level: Expert. Aligns with MCHbest strategy 15.6 "Continuous and Adequate Insurance” . Find other NPM 15 strategies in MCHbest.

Measurement Quadrant: Quadrant 4: Measuring quality of effect (% of "is anyone better off")

Service Type: Direct services level of pyramid

Essential Public Health Services: 7. Assure effective and equitable health systems

Service Recipient: Activities directed to families/children/youth

Goal: Increase the percentage of families receiving family-to-family support who report increased confidence in navigating care for their child

Numerator: Number of families who completed the post survey and reported increased confidence in a minimum of one area

Denominator: Number of families who received family-to-family support and completed the post survey

Significance: The strategy related to this measure is, “Building the Capacity of Communities by Cultivating Knowledge and Improving Collaboration.” One of Minnesota’s approaches toward building community capacity is funding family-to-family support. Through family-to-family support, the parent/caregiver is linked with another parent who helps answer their questions, provides support, and helps them navigate the system. After receiving family-to-family support, families typically report that they’re more knowledgeable of the system of care and are more competent/confident in navigating the system. Those who are more confident in their ability to navigate and access care may be more likely to have (or gain access to) adequate and consistent insurance.

Data Sources and Data Issues: Data Source: The percentage of families reporting increased confidence is collected via a survey that is distributed to parents by the family support grantee after the families have received their support. The survey is distributed to all families who have received support around 2 months after they have completed the service. In the survey, families are asked the following question: “Since receiving support and/or information, via email or phone, from someone with the CONNECTED Program, do you feel more confident in your ability to (Please check all that apply): • Get information about community resources, (such as financial information, PCA services, educational supports) when needed • Make decisions about your child’s healthcare • Navigate the healthcare system to get services your child needs • Take care of your child’s healthcare needs The grantee will provide MDH the data for the post-survey on a regular basis, and MDH will be responsible for analyzing the data to report on the ESM. The numerator will be the number of parents who checked off that they had increased confidence in at least one of the four areas listed above. The denominator is the total number of families who completed the survey after receiving family-to-family support. Limitations of Data: The data only includes those who completed the post-survey they were sent after receiving support and/or information. There may be a bias in the population who completes the survey versus those who do not. Another limitation is that the data is only gathered via post survey and is based on parent report. A potentially more valid way of gathering this information would be conducting a pre- and post-survey, where parents/caregivers could note the change they experienced from one point to the next.

Year: 2021

Unit Type: Percentage, Unit Number: 100

ESM 15.1 15.1 Increase the percentage of CYSHCN who report having insurance when receiving services (Washington)

Measure Status: Active

Evidence Level: **Not sure what they are doing - checked State Action plan in Box

Measurement Quadrant: Quadrant 4: Measuring quality of effect (% of "is anyone better off")

Service Type: Systems level of pyramid

Essential Public Health Services: 2. Investigate and address health problems

Service Recipient: Activities directed to families/children/youth

Goal: Increase the percent of CYSHCN who have access to third party paid insurance.

Numerator: The number of CYSHCN who indicate they have insurance on their Child Health Intake Form.

Denominator: The total number of CYSHCN who have a Child Health Intake Form filled out

Significance: Adequate insurance is critical for CYSHCN to receive needed services that their families can afford. Tracking the percent of CYSHCN receiving services will help to ensure that this population continues to be able to access care.

Data Sources and Data Issues: The data will come from the Child Health Intake Form (CHIF) a data collection instrument used in Washington State to track CYSHCN to assure they receive appropriate services. The form is filled out by county/local CYSHCN directors and/or neurodevelopmental centers.

Year: 2021

Unit Type: Percentage, Unit Number: 100

ESM 15.2 # of Children with Medical Complexities Advisory Committee (CMCAC) meetings and/or sub-committee meetings attended to improve support of these children included Medicaid coverage. (Delaware)

Measure Status: Active

Evidence Level: There is limited research in the evidence base for this NPM to support this strategy.

Measurement Quadrant: Quadrant 1: Measuring quantity of effort (counts and "yes/no" activities)

Service Type: Enabling services level of pyramid

Essential Public Health Services: 4. Support and mobilize partners

Service Recipient: Activities related to systems-building

Goal: For Title V/MCH to participate and stay engaged in the CMCAC meetings and share information with Family Shade and other CYSHCN partners.

Numerator: Number of meetings attended by Title V/MCH

Denominator: Count

Significance:

Data Sources and Data Issues: During development of Delaware’s Plan for Managing the Health Care Needs of Children with Medical Complexity (the Plan), it became evident early in the planning process that there would not be enough time to perform an in-depth analysis of the full continuum of care for children with medical complexity. The data needed to perform a quantitative analysis is very detailed and complex. Therefore, the first recommendation made as a result of the Plan development, was for DMMA to continue working with stakeholders to address the needs of this vulnerable population. As a result, the Children with Medical Complexity Advisory Committee (CMCAC) was developed. This group meets quarterly to strengthen the system of care, increase collaboration across agencies, encourage community involvement, and ultimately ensure that every child with medical complexity has the opportunity to receive the adequate and appropriate health care services they need and deserve.

Year: 2021

Unit Type: 4, Unit Number: MCH program data

ESM 15.3 % of primary caregivers and children with health insurance among Home Visiting participants (Delaware)

Measure Status: Active

Evidence Level: No similar strategy found in the established evidence for this NPM. See similar ESMs for this NPM or search for other strategies or promising practices.

Measurement Quadrant: Quadrant 2: Measuring quality of effort (% of reach; satisfaction)

Service Type: Systems level of pyramid

Essential Public Health Services: 7. Assure effective and equitable health systems

Service Recipient: Activities directed to families/children/youth

Goal: To increase the number of primary caregivers and children with health insurance

Numerator: # of primary caregivers and children (families) with health insurance

Denominator: # of families enrolled

Significance: Health insurance covers essential health benefits critical to maintaining generalhealth, preventive care, treating illness and accidents

Data Sources and Data Issues: MIECHV program data

Year: 2021

Unit Type: Percentage, Unit Number: 100

   

This project is supported by the Health Resources and Services Administration (HRSA) of the U.S. Department of Health and Human Services (HHS) under grant number U02MC31613, MCH Advanced Education Policy, $3.5 M. This information or content and conclusions are those of the author and should not be construed as the official position or policy of, nor should any endorsements be inferred by HRSA, HHS or the U.S. Government.