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The Effects of Case Management in a Medicaid Managed Care Plan

The Effects of Case Management in a Medicaid Managed Care Plan

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00385879
Enrollment
500
Registered
2006-10-11
Start date
2006-05-31
Completion date
2008-01-31
Last updated
2006-10-11

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

Conditions

Adrenal Cortex Diseases, Heart Diseases, Neoplasms

Brief summary

The purpose of this study is to evaluate whether or not case management by a social worker and nurse can decrease the number of emergency room visits, increase the number of primary care doctor visits, and increase quality of life of people in a Medicaid managed care plan.

Detailed description

This study will assign participants based on Zip Code to one of two conditions: control and experimental. In the control group, participants will receive telephonic assessments at baseline, three months, and six months. These assessments will be conducted by a member of the Medical Center's Department of Geriatrics under the supervision of the Principal Investigator. Participants in the experimental group will receive medical case management provided by a nurse and social worker in the homecare setting including an in-home assessment. Assessments will be conducted at baseline, three months, and six months during routine homecare visits. Dependent variables being measured include: access to primary care physicians, emergent hospitalizations/admissions, articulation of advance directives, and quality of life. Data will be collected through the participants' medical claims and records to analyze the number of emergent hospitalizations/admissions, documentation of advance directives, and number of visits to primary care physicians. To measure participants' quality of life, the Depression Self-Rating Scale and the Clinical Anxiety Scale will be utilized. Data will be compared between and within the groups via statistical analyses. The researcher will conduct pre-post comparisons of utilization and other database-derived outcomes for both groups, comparing the 12 months prior to and up to 20 months following enrollment.

Interventions

BEHAVIORALCase management

Sponsors

Metropolitan Jewish Health System
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* participation in a Medicaid managed care plan * resident of identified zip codes in Brooklyn, NY * frequent hospitalizations and low frequency of primary doctor visits

Exclusion criteria

* residents outside the catchment area * patients not being managed in a Medicaid managed care plan

Design outcomes

Primary

MeasureTime frame
The outcome measure for the number of emergency room visits will be calculated from the medical record counting the number of hospital emergency room visits; for access to primary physicians, the medical record will be reviewed as well.

Secondary

MeasureTime frame
The outcomes for quality of life will be evaluated from the McGill Quality of Life Questionnaire.

Countries

United States

Contacts

Primary ContactRussell E Hilliard, PhD, LCSW
rhilliar@mjhs.org718-491-7214
Backup ContactEliot Fishman, PhD
efishman@mjhs.org718-491-7134

Outcome results

None listed

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