Evaluating the Impact of Training for IHSS Workers

January 29, 2024 updated by: Abdul Latif Jameel Poverty Action Lab

This trial investigates whether high-quality training for consumer-directed home health workers impacts health outcomes for care consumers and employment outcomes for care workers. The investigators are conducting this study in the context of the In-Home Supportive Services (IHSS) program, a consumer-directed, Medicaid-funded home care program in California serving elderly and disabled Medicaid recipients. The investigators will partner with the Center for Caregiver Advancement (CCA), a training provider based in California, to conduct a randomized evaluation of the impact of training for IHSS workers on labor and health care outcomes. The evaluation will enroll IHSS workers in San Bernardino County, where CCA will be expanding its program.

Participants will be randomized to either a group that receives CCA's training or a control group that does not receive training.

Participants randomized to the training group will complete a 30 hour online course that teaches fundamental caregiving skills. Training includes personal care, infection control, nutrition and body mechanics, medication adherence, and home safety.

Researchers will compare outcomes between IHSS providers in the two groups and between IHSS consumers who receive care from the IHSS providers in the two groups to see if training impacts health, health care, and labor market outcomes.

Study Overview

Status

Recruiting

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

2500

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Current IHSS provider
  • Live in San Bernardino County
  • IHSS consumer lives in San Bernardino County

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: IHSS Basic Training
Individuals in the treatment group will be invited to participate in CCA's IHSS Basic training program. The program is a 30 hour online course for IHSS providers, which teaches fundamental caregiving skills. Training includes personal care, infection control, nutrition and body mechanics, medication adherence, and home safety.
The intervention is the Center for Caregiver Advancements 30-hour IHSS Basic training course.
No Intervention: Control
No intervention is delivered to the control group. The control group will be unable to access CCA's training programs for two years following random assignment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Number of emergency department visits (for consumer)
Time Frame: 1 year after training begins
1 year after training begins

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Any emergency department visits (for consumer)
Time Frame: 1 year after training begins
1 year after training begins
Estimated annual health care spending (for consumer)
Time Frame: 1 year after training begins
Estimated annual health care spending will be calculated by multiplying the number of inpatient admissions, emergency department visits, outpatient office visits, long term care stays, and prescription drugs by estimated average costs for those services among low income publicly insured adults.
1 year after training begins
Share of participants with falls resulting in a health care visit (for consumer)
Time Frame: 1 year after training begins
The share of consumers with falls will be measured using diagnosis codes from medical claims
1 year after training begins
Share of participants with urinary tract infections resulting in a health care visit (for consumer)
Time Frame: 1 year after training begins
The share of consumers with urinary tract infections will be measured using diagnosis codes from medical claims
1 year after training begins
Share of participants with pressure ulcers resulting in a health care visit (for consumer)
Time Frame: 1 year after training begins
The share of consumers with pressure ulcers will be measured using diagnosis codes from medical claims
1 year after training begins
Share of participants with nursing facility utilization (for consumer)
Time Frame: 1 year after training begins
The share of consumers who have a stay in a skilled nursing facility, rehab, or long term care facility during the year after training begins.
1 year after training begins
Share of participants still employed in IHSS (for provider)
Time Frame: 1 year after training begins
The share of IHSS provider participants who remain as workers in the IHSS program 1 year after the start of training.
1 year after training begins
Caregiving knowledge (for provider)
Time Frame: 0-3 months after completion of training
Proportion of correct answers out of 18 true false knowledge questions
0-3 months after completion of training
Total length of stay in nursing facilities (for consumer)
Time Frame: 1 year after training begins
The number of days spent per consumer in a skilled nursing facility, rehab, or long term care facility during the year after training begins.
1 year after training begins
IHSS earnings (for provider)
Time Frame: 1 year after training begins
IHSS earnings for providers, measured weekly, quarterly, and annually, drawn from IHSS payroll data
1 year after training begins
IHSS hours worked (for provider)
Time Frame: 1 year after training begins
IHSS hours worked for providers, measured weekly, quarterly, and annually, drawn from IHSS payroll data
1 year after training begins

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Any hospital admissions (for consumer)
Time Frame: 1 year after training begins
1 year after training begins
Number of hospital admissions (for consumer)
Time Frame: 1 year after training begins
1 year after training begins
Total length of stay in hospital (for consumer)
Time Frame: 1 year after training begins
1 year after training begins
Depression (for provider)
Time Frame: 0-3 months after completion of training
Patient Health Questionnaire-2 (PHQ-2). Scores range from 0 to 6, with higher values indicating worse outcomes. A score of 3 or higher identifies possible cases of major depressive disorder.
0-3 months after completion of training
Anxiety (for provider)
Time Frame: 0-3 months after completion of training
Generalized Anxiety Disorder 2-item (GAD-2). Scores range from 0 to 6, with higher values indicating worse outcomes. A score of 3 or higher identifies possible cases of generalized anxiety disorder.
0-3 months after completion of training
Caregiver wellbeing (for provider)
Time Frame: 0-3 months after completion of training
18 question caregiver self assessment questionnaire developed by the American Medical Association (https://www.healthinaging.org/tools-and-tips/caregiver-self-assessment-questionnaire). Includes 16 Yes/No questions and 2 scale of 1 to 10 questions, with higher values indicating worse outcomes. 10 or more yes answers, having crying spells, feeling completely overwhelmed, a stress rating of >=6 out of 10, or health rating of >= 6 out of 10 all indicate distress.
0-3 months after completion of training
Caregiver job satisfaction (for provider)
Time Frame: 0-3 months after completion of training
Self-reported answer to "Overall, how satisfied are you with your IHSS job?" on a 5-point Likert scale from very dissatisfied to very satisfied
0-3 months after completion of training
Number of consumers served (for provider)
Time Frame: 1 year after training begins
How many people the provider is paid to care for as part of the IHSS program
1 year after training begins

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Amy Finkelstein, PhD, Massachusetts Institute of Technology
  • Principal Investigator: Matthew Notowidigdo, PhD, University of Chicago
  • Principal Investigator: David Autor, Phd, Massachusetts Institute of Technology
  • Principal Investigator: Anna Russo, Massachusetts Institute of Technology

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 9, 2024

Primary Completion (Estimated)

June 30, 2027

Study Completion (Estimated)

June 30, 2029

Study Registration Dates

First Submitted

December 14, 2023

First Submitted That Met QC Criteria

January 3, 2024

First Posted (Actual)

January 16, 2024

Study Record Updates

Last Update Posted (Actual)

January 30, 2024

Last Update Submitted That Met QC Criteria

January 29, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 2308001081

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

To the extent allowed by our data use agreements with administrative data providers, we will share de-identified data and analysis code at the conclusion of the project.

IPD Sharing Time Frame

Data will become available after publication and will be hosted on a public research data repository such as the Harvard Dataverse (dataverse.org).

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ANALYTIC_CODE

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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