A Partnered Evaluation to Improve the Identification and Management of Functional Impairment and Frailty Among Older Veterans in Primary Care Settings

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age60+
SponsorVA Office of Research and Development

About this trial

Maintaining functional status, or the ability to perform daily activities, is central to older adults' quality of life, health, and ability to remain independent. Identifying functional impairments is essential for clinicians to provide optimal care to older adults, and on a population level, understanding function can help anticipate service needs. Yet uptake of standardized measurement of functional status into patient care has been slow and inconsistent due to the burden posed by current tools. The purpose of the proposed QUERI Partnered Evaluation Initiative is to implement and evaluate a patient-centered, low-burden intervention to improve measurement of functional status in VA primary care settings nationally. The investigators hypothesize that implementing this intervention will increase identification and improve management of functional impairment among older Veterans while providing key data to inform VHA strategic planning related to long-term services and supports.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Veteran

>60 years old

Seen in Veterans Health Administration primary care after implementation begins

Disqualifiers

Non-Veteran

<60 years old

Not seen in Veterans Health Administration primary care

Trial design

Design model

Crossover

Treatments tested in this trial

  • Screening intervention

    Other intervention

    Intervention to improve identification and management of functional impairment among older Veterans in VA primary care settings. Intervention includes 5 components: (1) routine, standardized functional status measurement; (2) nursing screening followed by follow-up primary care provider assessment; (3) electronic tools and templates to facilitate screening, assessment, and documentation; (4) interprofessional educational session; (5) tailored reports on functional status

  • Standard bundle of implementation strategies

    Other intervention

    Standard strategies include champions plus system-level audit and feedback

  • Enhanced bundle of implementation strategies

    Other intervention

    Enhanced strategies include technical assistance plus clinician-level audit and feedback

Treatment groups

10,000 Participants
are divided into 2 treatment groups
Group A: Functional status screening initiative plus standard bundle of implementation strategiesActive comparator 2 interventions
Group B: Functional status screening initiative plus enhanced bundle of implementation strategiesExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Change in reach

Reach is defined as the proportion of eligible Veterans who receive LVN screening and PCP assessment at each center. The investigators will identify eligible Veterans (i.e., 60 years old, seen in primary care after implementation begins) and use Health Factors to identify completed screening, defined as an LVN completing the electronic tool, and assessment, defined as a PCP reviewing screening results and either (a) documenting via checkbox that further referral is not needed or (b) placing a referral to address impairments.

Time frame
9 months, 12 months, 15 months, 18 months, 24 months
2

Change in clinical effectiveness

The primary outcome is proportion of Veterans with impairments who receive appropriate referrals. Appropriate referrals will be defined as the PCP reviewing the LVN screening results and either (1) documenting via checkbox that further referral is not needed or (2) placing a referral to address identified impairments.

Time frame
0 months, 9 months, 12 months, 15 months, 18 months, 24 months
3

Change in association of electronic health record frailty indices with functional status

Frailty will be measured using the validated VA Frailty Index (VA-FI), calculated using the cumulative deficit method. The VA-FI includes up to 31 age-related health deficits based on VA EHR diagnostic and procedure codes. Categories include non-frail (0-0.1), pre-frail (0.11-0.2), and frail (\>0.2). Functional status will be measured from Health Factors. In sensitivity analyses, the investigators will examine other EHR frailty indices (e.g., JEN Index100)

Time frame
0 months, 9 months, 12 months, 15 months, 18 months, 24 months

Secondary outcomes

1

Change in adoption

Adoption is defined as (1) the proportion of LVNsat each medical center who regularly complete screening; and (2) the proportion of PCPs at each medical center who regularly complete assessment. Adequate adoption for each clinician-type is defined as 80%.

Time frame
0 months, 9 months, 12 months, 15 months, 18 months, 24 months
2

Change in adoption in clinician notes

The investigators will review a subset of charts at the 6 sampled centers to examine if clinician notes for the visit when screening was completed have content related to functional status and type of content.

Time frame
0 months, 9 months, 12 months, 15 months, 18 months, 24 months
3

Change in fidelity

Fidelity to implementation strategies will be measured using Managerial Champion attendance at VISN-level monthly meetings (standard strategy) or technical assistance calls (enhanced strategy). Fidelity to intervention core components will be measured at the 6-site subsample to determine if core components were implemented as intended, accounting for adaptations and modifications that were consistent vs. inconsistent with intent.

Time frame
0 months, 9 months, 12 months, 15 months, 18 months, 24 months
4

Recipient experience

Recipient experience will be assessed using interviews for Veterans and periodic reflections and interviews for clinicians and will be used to inform adaptations to intervention components and implementation strategies. To operationalize processes within PRISM's Adoption, Implementation, and Maintenance domains, the investigators will use Normalization Process Theory (NPT) to guide qualitative data collection.

Time frame
Through study completion, from 0 to 24 months

Other outcomes

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