Research Questions. Respite and Developmental Disabilities. Respite Care Some background. Flexible Funds: What we know

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Use of Flexible Funds for Services in a Managed Care Wraparound program Jennifer Taub Ph.D., UMass Medical School Joseph O Garr, B.S., UMass Medical School Jack Simons, Ph.D., Coordinated Family Focused Care, Lawrence, MA Kim Smith, M.A. UMass Medical School Presented as part of the symposium: Financing Issues in Systems of Care for Children s Mental Health At the18th Annual Research Conference: A System of Care: Expanding the Research Base March 6-9, 2005 University of South Florida, Tampa, FL Please direct any inquiries to the first author: jennifer.taub@umassmed.edu Center for Mental Health Services Research University of Massachusetts Medical School 305 Belmont St., Room 8C-29 Worcester, MA 01604 Coordinated Family-Focused Care Research Questions There are many unanswered questions about the use of flexible funds to support community based services for children with serious emotional disturbance (SED). This presentation focuses on the use of flexible funds to support respite services for this population. Study Questions: 1. What types of respite programs are accessed with flexible funds (in-home vs. out of home)? 2. What are the costs associated with these services on the program and individual client levels? 3. What is the relationship between child functioning and use of respite services? 4. What is the relationship between child factors and use of respite services? Care Some background and Developmental Disabilities The majority of research focuses on the developmentally disabled population and the effect of respite on caregiver stress. care has been defined as temporary care given to a disabled individual for the purpose of providing an interval of relief to the individual s primary caregiver(s). (Cohen, 1982, p.8) can occur as Crisis vs. planned In-home vs. out-of-home or overnight In general, families prefer in-home respite care (Cohen, 1982; Boothroyd, 1998) Some new data shows parents prefer out-of-home respite and demonstrates a discrepancy between family and caseworker preferences (MacDonald & Callery, 2004) Evidence suggests there are no significant demographic differences between groups of respite users and nonusers (Wherry et al, 1995) In-home and out-of-home respite is effective in reducing caregiver stress in families of children with developmental disabilities (Rimmerman, 1989; Mullins et al, 2002; Chan and Sigafoos, 2001) and Serious Emotional Disturbance Flexible Funds: What we know care is described as an important social service often needed by families of children with SED (Stroul & Friedman,1986). Case-workers of children with SED estimate that approximately 7% of families in their caseloads require respite care services (Trupin, 19). Children of parents who utilized respite care tend to be younger and have a higher number of functional impairments (Boothroyd et al, 1998). care users reported less availability of social supports and more difficulty managing their child s behavior (Boothroyd et al, 1998). In a wait-list controlled longitudinal study involving both in-home and out-of-home respite, respite care resulted in: reduction of caregiver personal strain fewer incidents of out-of-home placement dose effect with increased use resulting in reduced out-of-home placement and increased family optimism (Bruns & Burchard, 2000) One published study has described the use of flexible funding dollars in providing supports for children with SED. These dollars are used for services such as respite care as part of a wraparound service program (Dollard et al, 1994) Only one other study has looked at child factors and flexible funds spending. It demonstrated that: Higher CAFAS scores predict higher Medicaid reimbursements The only factor predictive of case management hours and flexible fund spending was a previous history of psychiatric hospitalization (Jenson et al, 2002) 1

Coordinated Family Focused Care (CFFC) The Child and Family Team What is CFFC? It s a five site wraparound services Care program for children with Severe Emotional Manager (Clinician) Disturbance (SED) at risk for out-of-home placement in Massachusetts. How are children eligible for CFFC? atural Caregiver Supports Ages 3-18 Family (e.g. Partner Child Reside in one of the 5 cities where it is offered eighbor, (advocate) Family Members Pastor, Child and Adolescent Functional Assessment Score Coach) of 100 or greater Presence of Severe Emotional Disturbance (SED) Formal Caregiver willing to participate in team process Supports (e.g. Child and family have tried other, less intensive, Therapist, Teacher) services 8 CFFC Services and Outcomes Flexible Funding in CFFC Wraparound Principles Child & Family Team Child & Family Team Community Based Services & Support Voice and Choice Individualized, Culturally Competent & Strengths-Based atural Supports Flexible Funding Program Goals Increase Family Involvement Parent Empowerment & Competency Child Functioning Child Strengths Reduce Out of Home Placement Cost Clinical Symptoms Parental Stress Outcome Measures Child s Mental Health Child s Strengths Child s Functioning Child s Functioning Parental Involvement Parental Stress $$$$ Costs Treatment Fidelity 9 The CFFC case rate is $62.22/child per day (based on a 365 day year); $1892 per child per month. Programs are expected to use approximately 20% of the case rate for services that are deemed necessary by the team and cannot be paid through other funding mechanisms. These Flexible Funds can be used to support client-level services and supports (e.g. summer camp) as well as programlevel services and supports (e.g. dinners for weekly Family ights for all families in the program). Programs may distribute funds across caseload as determined by clinical needs. They do not need to spend a set amount on each child, but the CFFC provider must guarantee that there are adequate funds to meet the needs of every child in the program. These Flexible Funds are subdivided into seven categories. Flexible Funding Categories in CFFC 1. Recreational: Recreational activities, after school and summer programs. Activities that enhance social skills and peer interactions. This also includes activities that strengthen family interactions. 2. Concrete supports: Purchases that support the family s ability to provided food, shelter, utilities, and related essentials that address short-term emergency needs. 3. In-home and community supports: Includes any 1:1, specialing or sitter services in the child s home or a community setting 4. Out of home respite/placement:, either crisis or planned, that occurs out of the home in a foster home, group home, or residential program, which is not otherwise paid for by insurance. 5. on-medically-ecessary Transportation: Taxi vouchers, gas cards or other arrangements to assist with transportation to school meetings, care plan meetings or program activities. 6. Meeting attendance: Supports attendance by payment to formal and informal supports who would not otherwise be compensated to attend care planning Team meetings or Local Committee meetings. 7. Other: Any other service or purchase for a specific child and their family, or for the CFFC program in general. Examples include food, gifts, transportation not covered by above category. What types of respite programs are accessed with flexible funds (in-home vs. out of home)? care used in each community reflect the available services and supports in that community Services change and develop over time as relationships are developed with community providers, and as community resources are accessed and developed A variety of programs and services are utilized In-home respite: Specialized babysitting, mentoring Out-of-home respite: Planned stays at crisis units, other established community programs; respite foster care for short term planned stays Programs face challenges in helping families access respite resources 2

Flexible Fund Spending over one year Total CFFC flexible funds spending Meeting Supports 0% Other 3% $250,000 Transportation 4%,000 Concrete 19% In-Home & Community Supports 49% $150,000 $100,000 Other Meeting Supports Transportation Concrete Recreational Out-Of-Home In-Home Recreational 23% Out-Of-Home 2% $50,000 10/03-12/03 1/04-3/04 4/04-6/04 7/04-9/04 Percent of Children Utilizing Overall per child spending After 3 in the program, 37% of children had received some form of respite 6 214 9 162 12 By 6, 60% had received respite By 9, 70% had received respite By 12, 78% had received respite Mean Median Mode Std. Deviation Range $599.54 $127.50 $1014.53-7197 $1096.94 $571.50 $1636.26 11,374 $1784.90 $1043.00 $2836.97 18,621 Sum $128,303 $177,705 $162,426 In-Home spending by Quarter by child by Site: 9 (Average per child =162) Overall spending by Quarter by child by Site: 12 (Average per child =87) Site 1 (n=28) Site 2 (n=40) Site 3 (n=27) Site 4 (n=27) Site 5 (n=40) Overall Sites 2 and 3 are significantly different from the others Site 1 (n=19) Site 2 (n=21) Site 3 (n=7) Site 4 (n=19) Site 5 (n=21) Overall Q1 Q2 Q3 Q1 Q2 Q3 Q4 3

In Home by Quarter by Gender (=) Intake DSM Axis I diagnoses (=187) 60% $900 $700 50% 40% 1 dx only = 48% 2 diagnoses = 30% 3 or more diagnoses = 22% $500 Female (n=22) Male (n=69) 30% 20% $300 Between groups p<.05 10% $100 Q1 Q2 Q3 Q4 0% ADHD Disruptive Behavior PTSD Bipolar Depression Thought Disorder Learning Disorder Anxiety Asperger's Reactive Attachment spending by DSM Diagnosis (=135) spending by Diagnoses (=135) $2,000 $700 $500 $300 $100 Overall (=135) Bipolar (=31) ADHD (=80) Disruptive Behavior (=36) PTSD (=38) Psychotic Dx (=14) Depressive Dx (=25) $1,800 $1,600 PTSD (=32) Depression (=19) PTSD + Depression (=6) either Dep or PTSD (n=78) Q1 Q2 Q3 1st Q 2nd Q 3rd Q Child Functional Impairment: Child and Adolescent Functional Assessment (CAFAS) Hodges, K. (2003) The CAFAS is a clinician rated assessment of impairment in youth with emotional, behavioral, or substance abuse problems. It has 8 subscales which are each rated to assess the level of impairment in each individual area. Each scale is rated o impairment, Mild, Moderate, or Severe. Total CAFAS Scores can range from 0-240. The subscales are: 1.School/Work Performance: assesses ability to function in a group environment 2.Home Role Performance: assesses youth s ability to follow reasonable rules and perform age appropriate tasks 3.Community Role Performance: assesses the respect for the rights of others and their property and conformity to laws 4.Behavior Toward Others: assesses youth s daily behavior toward others 5.Self Harmful Behavior: assesses the extent to which the youth can cope without resorting to self harmful behavior 6.Moods/Emotions: assesses the youth's control over his or her emotions 7.Substance Use: Youth s substance use and the extent to which it is maladaptive or disruptive to normal functioning 8.Thinking: assesses the youth s ability to use rational though processes Child s Mental Health Status: Youth Outcome Questionnaire (YOQ) Burlingame, G. M., Wells, M.G. & Lambert, M. J. (1996) A Standardized, reliable and valid parent-completed symptom checklist. Contains 64 items completed on a 1-5 Likert scale (ever to Frequently) over previous 7 days. Contains 6 subscales: 1. Intrapersonal Distress (ID): Anxiety, depression, fearfulness, hopelessness and self-harm. 2. Somatic (S) 3. Interpersonal Relations (IR): Communication and interaction with friends, cooperativeness, aggressiveness, arguing, and defiance. 4. Social Problems (SP): Delinquent or aggressive behaviors; includes substance abuse. 5. Behavioral Dysfunction (BD): Organization, concentration, hyperactivity, impulsivity. 6. Critical Items (CI): Describes features of children and adolescents often found in inpatient services where short-term stabilization is the primary change sought. Includes paranoid ideation, obsessive-compulsive behaviors, hallucinations, delusions, suicidal feelings, mania, and eating disorder issues. 4

s between $ and child factors Predictors of Spending Somatic Score (YOQ) $ Q1.203(**) 0.002 $ Q2.243(**) $ Q3.196(*) 0.016 $ Q4.362(**) 6 9 12.261(**).254(**).425(**) 0 0.002 0 Months in the Program R R Square Adjusted Std. Error of the R Square Estimate F Predictors in the Model 6 125.330.109.094 1119.158 7.512** Somatic YOQ $58 PTSD $481 9 110.421.177.154 1689.148 7.692*** Somatic YOQ $77 $ PTSD (DSM DX) CAFAS Self harm 237.180(*) 0.015 180 0.113 0.066 195 0.15 0.058 161 0.081 0.241 151.224(**) 0.009 135.185(*) 0.018 82.359(**) 86 0.162 0.124 195.189(*) 0.016 161 0.125 0.069 151.236(**) 0.006 135.156(*) 0.047 82.386(**) 0 86 0.202 0.055 PTSD $994 CAFAS Self $330 Harm 12 67.604.365.336 2583.735 12.276*** Somatic YOQ $199 PTSD $2443 CAFAS Self Harm $597 265 212 162 ** is significant at the 0.01 level (2-tailed) * is significant at the 0.05 level (2-tailed) 212 162 *** Significant at the.0001 level ** Significant at the.001 level Summary of findings Summary of findings In-home respite is the largest category of flex fund spending, accounting for about half of all flex dollars spent in the program. Most children (over 60%) receive this service at some point during their enrollment. Out-of-home is not a highly utilized service paid from flexible funding. Less than 10% of enrolled children ever receive this service. We have discovered several predictors of utilization of respite services in our wraparound program: A DSM diagnosis of PTSD Higher level of Somatic complaints (Intake YOQ) and CAFAS Self Harm subscale (Intake) are all predictive of respite spending. There is a difference in respite spending on girls vs. boys (more is spent on girls) over a 12 month period (this difference is not significant at 6 or 9 ). This is not accounted for by the factors listed above. Although children with co-morbidity have higher overall respite costs, this factor in and of itself is not a statistically significant predictor of respite costs. Data also revealed some trends to watch: Lower respite costs for children with ADHD Much higher respite costs for children who are comorbid with Depression + PTSD References Boothroyd, R. A., et al. (1998). Understanding respite care use by families of children receiving short-term, inhome psychiatric services. Journal of Child and Family Studies, 7(3), 353-376. Bruns, E. J., & Burchard, J.D. (2000) Impact of respite care services for families with children experiencing emotional and behavioral problems. Children s Services: Social Policy, Research, and Practice, 3(1), 39-61. Burlingame, G., Wells, M.G., & Lambert, M.G. (1996) American Professional Credentialing Services. Chan, J.B., & Sigafoos, J. (2001). Does respite care reduce parental stress in families with developmentally disabled children. Child & Youth Care Forum, 30(5), 253-263. Cohen, S. (1982). Supporting Families Through Care. Rehabilitations Literature, 43(1-2), 7-11. Hodges, K., Doucette-Gates, A., & Kim, C.-H. (2000). Predicting service utilization with the Child and Adolescent Functional Assessment Scale in a sample of youths with serious emotional disturbance served by Center for Mental Health Services-funded demonstrations. The Journal of Behavioral Health Services & Research, 27(1), 47-57. Jenson, C.E. et al (2002) Predicting resource utilization by children with serious emotional disturbance and their families. Journal of Child and Family Studies, 11(3), 361-371. Macdonald, H. & Callery, P. Different meanings of respite: a study of parents, nurses and social workers caring for children with complex needs. Child: Care, Health & Development. 30(3), 279-288. Mullins, L.L., et al. (2002). The influence of respite care on psychological distress in parents of children with developmental disabilities: A longitudinal study.children s Services: Social Policy, Research, and Practice, 5(2), 123-138. Rimmerman, A. (1989). Provision of respite care for children with developmental disabilities: Changes in maternal coping and stress over time. Mental Retardation, 27(2), 99-103. Stroul, B.A & Freidman, R.M. (1986) A system of care for children and youth with severe emotional disturbances. (Revised edition). Washington, DC: Georgetown University Child Development Center, CASSP Technical Assistance Center. Trupin, E. W., Forsyth-Stephens, A., and Low, B.P. (19). Service needs of severely disturbed children. American Journal of Public Health, 81, 975-980. Warren, R. & Cohen, S. (1985). Care. Rehabilitation Literature, 46(3-4), 66-71. Wherry, J.., Shema, S.J., Baltz, T., & Kelleher, K. (1995). Factors associated with respite care use by families with a child with disabilities. Journal of Child and Family Studies, 4(4), 419-428. 5