Skip to content

Community Health Worker Intervention to Improve Post-Hospital Outcomes

Community Health Worker and Certified Peer Specialist Intervention to Improve Post-Hospital Outcomes

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04028609
Acronym
CHW
Enrollment
55
Registered
2019-07-22
Start date
2019-09-12
Completion date
2020-03-09
Last updated
2023-04-28

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

Conditions

Chronic Disease (Physical), Mental Disorder

Keywords

30-day readmission, primary care, community health worker, health education

Brief summary

This study tests an intervention designed to avoid 30-day readmissions following a medical hospitalization by patients who have co-occurring mental illness. The Intervention is delivered by community health workers in the inpatient setting and 30 days following hospital discharge to the community.

Detailed description

This study will test the efficacy of a brief intervention delivered to adults with co-occurring medical and mental health conditions by community health workers designed to avoid 30-day readmissions following medical hospitalization. Adult inpatients of a university hospital will be randomly assigned to the intervention plus services as usual versus services as usual alone, and assessed at baseline and 30 days following discharge. Chi square will be used to assess the primary outcome of admission within 30 days of discharge and changes in patient activation, mental health symptoms, medication adherence, and perceived competence for health maintenance. Also examined will be study condition differences in post-discharge inpatient service utilization and cost.

Interventions

BEHAVIORALHealthy at Home

In addition to receiving medical services as usual, subjects receive services from Community Healthy Workers during the transition from the hospital to their community residence.

OTHERServices as Usual

Routine medical services

Sponsors

National Institute on Disability, Independent Living, and Rehabilitation Research
CollaboratorFED
Substance Abuse and Mental Health Services Administration (SAMHSA)
CollaboratorFED
University of Illinois at Chicago
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Research interviewers were blinded to study condition.

Intervention model description

The intervention includes 4 components: development of a personal health plan; review and support for medication adherence; connection with primary care provider within 30 days; and education about clinical indicators that call for immediate intervention.

Eligibility

Sex/Gender
ALL
Age
21 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* receiving inpatient treatment for chronic medical condition * evidence of a mental health diagnosis * age 21- 60 years * expected to return to community residence * residing within a 30-mile radius of the hospital * expected to remain in hospital for 2 or more days * able to provide informed consent

Exclusion criteria

* terminally ill * unable to communicate in English * expected to be discharged to skilled facility or nursing home * participating in another transitional care intervention * hospitalized for behavioral health disorder

Design outcomes

Primary

MeasureTime frameDescription
Federal Center for Medicare and Medicaid Services' measure of unplanned readmissions that occur within 30 days of discharge from an initial admission30 days post dischargeThis is a dichotomous indicator variable that reports the occurrence of an inpatient admission to the hospital within 30 days of discharge from a previous hospitalization. Score ranges from 0 (no readmission) to 1 (readmission).
Federal Center for Medicare and Medicaid Services' measure of completion of a outpatient visit with primary care providerduring the 30 days period following dischargeThis is a dichotomous indicator variable that reports the completion of a patient's visit to an outpatient primary care provider

Secondary

MeasureTime frameDescription
Short Form Health Surveystudy entry (pre-intervention), 30 days post discharge (post intervention)This scale measures the construct of self-reported physical and emotional health by asking about functioning (e.g., climbing stairs, doing housework) and emotional well-being (e.g., feeling calm and peaceful, being downhearted or blue). Total score ranges from 12 to 44 with higher values indicating better health. Total score is the sum of all item responses.
Health Care Climate Questionnairestudy entry (pre-intervention), 30 days post discharge (post intervention)This scale measures the construct of a patients' perception of their medical care as as providing needed information, acknowledging their feelings, and supporting their autonomy. Total score ranges from 1 to 7 with higher values indicating greater autonomy. Total score is calculated by averaging the item scores.
Center for Disease Control and Prevention's National Health and Nutrition Examination Survey of Usual Source of Medical Carestudy entry (pre-intervention), 30 days post discharge (post intervention)These items from a national household survey ask respondents about their access to and type of usual source of medical care. Both items are categorical self-report questions designed to yield descriptive information with no scoring.
Patient Activation Measurestudy entry (pre-intervention), 30 days post discharge (post intervention)This scale measures the construct of a person's self-perceived ability to engage in health care. Items assess patients' self-perceived level of knowledge, skill, and confidence in their ability to manage their own health. Total score ranges from 13 to 52 with higher values indicating greater activation. Total score is calculated by summing items to create a raw score which is then divided by the number of items answered and multiplied by 13 and transformed to a Z score based on calibration tables.
Patient Health Questionnaire-2study entry (pre-intervention), 30 days post discharge (post intervention)This is a screening questionnaire for depression and anhedonia that measures the extent to which respondents report that they are sad, hopeless, and have little interest in doing things. Total score ranges from 0 to 6 with higher values indicating greater likelihood of depressive disorder. Total score is calculated by adding the 2 item scores.
Generalized Anxiety Disorder 2-item Questionnairestudy entry (pre-intervention), 30 days post discharge (post intervention)This is a screening questionnaire for generalized anxiety disorder that measures the extent to which respondents report that they are nervous, anxious, or continually worried. Total score ranges from 0 to 6 with higher values indicating greater likelihood of generalized anxiety disorder. Total score is calculated by adding the 2 item scores.
Patient Satisfaction Questionnairestudy entry (pre-intervention), 30 days post discharge (post intervention)This a questionnaire that measures the construct of patients' satisfaction with their medical provider by asking them to rate their doctor's communication, time spent, and overall satisfaction. Total score ranges from 6 to 30 with higher values indicating greater satisfaction. Total score is calculated by adding the item scores.
Perceived Competence for Health Maintenance Questionnairestudy entry (pre-intervention), 30 days post discharge (post intervention)This scale measures the construct of self rated ability to manage one's health condition, engage in routine health care, and recover from a medical condition. Total score ranges from 1 to 7 with higher values indicating greater competence. Total score is calculated by averaging scores of the 4 items.

Countries

United States

Outcome results

None listed

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