SB2400 — HOSPICE DATA COLLECTION
Last action — Rule 2-10 Committee/3rd Reading Deadline Established As May 15, 2026
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1Introduced
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2In Committee
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3Passed Senate
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4Passed House
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5To Executive
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6Enacted
This bill has been introduced in the Senate. Introduced February 07, 2025. It must pass committee before a floor vote.
Next likely step: a committee referral and hearing.
Odds of enactment
Low chanceBased on the sponsor, cosponsors, and committee posture, this bill has a low chance of becoming law.
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A statistical estimate from our own model of past outcomes — an insight, not a guarantee. Policymaking is volatile.
Prognosis
Not enough signal yet to read this bill's trajectory — we surface a likelihood only once there's real movement (stage, sponsorship, committee, or votes) to point to.
Based on stage, sponsorship breadth, committee status, recorded votes, and cross-state momentum — a description of the observable signals, not a prediction.
Summary
Amends the Hospice Program Licensing Act. Requires the Department of Public Health to develop and implement a standardized system for collecting data from hospice providers across the State. Provides that the data shall include demographic information of hospice patients, including age, race, gender, and geographic location; service utilization metrics, such as average length of stay in hospice care and types of services provided; patient and family satisfaction data, collected through voluntary surveys; and workforce data, including the availability and turnover rates of hospice staff. Requires the data to be collected in compliance with applicable federal and State privacy laws. Provides that the Department shall compile an annual report summarizing key findings from the collected data, and requires the report to be submitted to the Governor and General Assembly and made publicly available on the Department's website.
Bill Text
We don't have the full text on file for this bill yet.
Read SB2400 on the official Illinois source →Action History
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Rule 2-10 Committee/3rd Reading Deadline Established As May 15, 2026
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Referred to Assignments
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First Reading
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Filed with Secretary by Sen. Bill Cunningham
Sponsors
- Bill Cunningham · Primary
Sponsorship breakdown
Export CSV (upgrade) →1 sponsors · 0 co-sponsors · 182 not signed on
Sponsors (1)
- Bill Cunningham Democrat
Co-sponsors (0)
None.
Not signed on (182)
182 members have not signed on to this bill.
Show all 182 →"Not signed on" means a member has not sponsored or co-sponsored this bill — it does not imply opposition. Members flagged Voted No have a recorded No vote on this bill.
Subjects
Frequently asked questions
- What does SB2400 do?
- Amends the Hospice Program Licensing Act. Requires the Department of Public Health to develop and implement a standardized system for collecting data from hospice providers across the State. Provides that the data shall include demographic information of hospice patients, including age, race, gender, and geographic location; service utilization metrics, such as average length of stay in hospice care and types of services provided; patient and family satisfaction data, collected through voluntary surveys; and workforce data, including the availability and turnover rates of hospice staff. Requires the data to be collected in compliance with applicable federal and State privacy laws. Provides that the Department shall compile an annual report summarizing key findings from the collected data, and requires the report to be submitted to the Governor and General Assembly and made publicly available on the Department's website.
- Who sponsors SB2400 ?
- SB2400 is sponsored by Bill Cunningham (Democrat).
- What is the current status of SB2400 ?
- This bill has been introduced in the Senate. Introduced February 07, 2025. It must pass committee before a floor vote.
- Where can I track SB2400 ?
- Track SB2400 free on One Click Politics — get push/email alerts when it moves.
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Last checked for changes 3 months ago · updated continuously
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