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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05910736
Other study ID # R01AG081996-01
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 1, 2024
Est. completion date July 2028

Study information

Verified date April 2024
Source University of California, Los Angeles
Contact Danielle Schramm, MSPH
Phone 310-794-8242
Email dschramm@mednet.ucla.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this study is to improve the use of preventive health services by implementing a multilevel intervention to stimulate Annual Wellness Visit use in diverse practices across the United States. This is a stepped wedge cluster randomized controlled trial. The intervention will be implemented in a total of 24 primary care practices over 24 months. Every 3 months, 6 practices will receive the intervention. Electronic health record (EHR) data extractions will be used to collect outcomes in a population cohort of patients. Semi-structured interviews will be conducted with clinicians/staff and patients to assess intervention implementation. The investigators hypothesize that the implementation will increase AWV visit use and consequently, use of preventive health services.


Description:

Older adults vastly underutilize evidence-based preventive health services that are proven to reduce serious illness, morbidity and mortality. In fact, fewer than half of adults aged 65 and older are up-to-date on evidence-based cancer screenings and vaccinations recommended by expert committees (e.g., the USPSTF and CDC/ACIP). Those at greatest risk for receiving poor preventive care include racial and ethnic minority groups and persons of low socioeconomic status. Yet interventions to remedy this underutilization in older adults have mostly targeted individual preventive health services, rather than the totality of services needed by patients. The 2011 Medicare establishment of the Annual Wellness Visit (AWV) is a great and underused opportunity to respond to the National Cancer Institute's calls for multilevel interventions that address both the supply and demand for vastly underutilized preventive health services. This free-to-the-patient AWV visit gives providers dedicated time to focus on preventive health services. The investigators developed a multilevel intervention to increase AWV use that successfully increased AWV utilization in 3 small (2-5 provider) pilot practices. The intervention addresses the complexities of increasing AWVs at patient (demand for services), provider (supply of services), and practice levels. It combines electronic health record (EHR)-generated information and tools with practice redesign tools and approaches to inform providers and patients about the preventive health services needed by individual patients. This proposal's goal is to conduct a pragmatic trial to evaluate the effect of the intervention on increasing AWV and preventive health services utilization. The investigators will implement the intervention in geographically and racially/ethnically diverse community-based practices, Federally Qualified Health Centers, and academic health system practices. Practices include small to mid-size primary care practices (including solo practices), which typically are under-represented in research. Specific aims of this study are to: 1) Evaluate the effect of the intervention on use of a) AWVs and b) USPSTF and CDC/ACIP-recommended preventive services in 3 different types of practice settings; 2) Evaluate the effect of the intervention on reducing racial/ethnic disparities in AWV utilization; and 3) Evaluate factors affecting implementation and sustainability of the intervention tools and approaches, implementation strategies, and intervention effect in diverse patient settings. Implemented via video conferencing and remote deployment of EHR tools, this low-cost intervention could easily be disseminated to small and solo practices across the country. The anticipated increase in patient use of preventive health services will improve population health and lower mortality, particularly in at-risk racial/ethnic minority patients. The intervention will be carried out sequentially in 24 primary care practices across the United States over 24 months. Every 3 months, 6 practices will receive the intervention. Many of the practices expected to participate in the study care for predominantly minority patients. Primary endpoints to be measured include: 1) rates of AWV use, and 2) completion of preventive health services recommended by the United States Preventive Services Task Force (USPSTF), CDC, and ACIP. The investigators hypothesize that the intervention will increase rates of AWV use, and in turn will result in greater completion of recommended preventive health services. The investigators also expect it to decrease racial/ethnic disparities in AWV utilization.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 22485
Est. completion date July 2028
Est. primary completion date July 2027
Accepts healthy volunteers No
Gender All
Age group 50 Years and older
Eligibility There are no inclusion or exclusion criteria based on sex/gender, race, and/or ethnicity. Inclusion Criteria: - have Medicare coverage - aged 50 or older - has at least one visit to the practice in the past 12 months - not deceased Practice eligibility criteria: • care for patients with Medicare insurance

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Medicare AWV Practice Redesign Toolkit
Electronic health record-based tools coupled with practice redesign strategies and approaches

Locations

Country Name City State
n/a

Sponsors (5)

Lead Sponsor Collaborator
University of California, Los Angeles American Academy of Family Physicians National Research Network, Case Western Reserve University, DARTNet, The MetroHealth System

Outcome

Type Measure Description Time frame Safety issue
Primary AWV utilization % of eligible patients completing an AWV (CPT codes G0438 or G0439) or Initial Preventive Physical Examination (IPPE) (CPT code G0422) in the past 12 months 12 months after intervention implementation in all practices
Primary AWV utilization % of eligible patients up to date on their AWV (CPT codes G0438 or G0439) or Initial Preventive Physical Examination (IPPE) (CPT code G0422) 24 months after intervention implementation in all practices
Primary Composite preventive health services score composite score representing % of all recommended preventive health services that a patient has fulfilled 12 months after intervention implementation in all practices
Primary Composite preventive health services score composite score representing % of all recommended preventive health services that a patient has fulfilled 24 months after intervention implementation in all practices
Secondary Utilization of recommended preventive health services % of patients up to date on each of the preventive health services listed below.
Vaccinations
Influenza vaccine
Herpes zoster vaccine
Pneumococcal vaccine
Tetanus vaccine
Cancer screening
Colorectal cancer screening
Mammogram
Pap smear
Other screening / counseling
Osteoporosis screening
Hepatitis C screening
Alcohol misuse screening
Depression screening
Tobacco use screening
Advance care planning
12 months after intervention implementation in all practices
Secondary Utilization of recommended preventive health services % of patients up to date on each of the preventive health services listed below.
Vaccinations
Influenza vaccine
Herpes zoster vaccine
Pneumococcal vaccine
Tetanus vaccine
Cancer screening
Colorectal cancer screening
Mammogram
Pap smear
Other screening / counseling
Osteoporosis screening
Hepatitis C screening
Alcohol misuse screening
Depression screening
Tobacco use screening
Advance care planning
24 months after intervention implementation in all practices
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