Stakeholder-informed pragmatic trial protocol of the TabCAT-BHA for the detection of cognitive impairment in primary care.


Journal

BMC primary care
ISSN: 2731-4553
Titre abrégé: BMC Prim Care
Pays: England
ID NLM: 9918300889006676

Informations de publication

Date de publication:
06 Aug 2024
Historique:
received: 07 06 2024
accepted: 25 07 2024
medline: 7 8 2024
pubmed: 7 8 2024
entrez: 6 8 2024
Statut: epublish

Résumé

Cognitive impairment and dementia are frequently under-recognized. Health system strategies anchored in primary care are essential to address gaps in timely, comprehensive diagnosis. The goal of this paper is to describe the adaptation of a tablet-based brain health assessment (TabCAT-BHA) intervention and the study protocol to test its effectiveness in improving the detection of cognitive impairment, including dementia. This mixed-methods, pragmatic, cluster randomized, hybrid effectiveness-implementation trial is being conducted in two 18-month waves with 26 Kaiser Permanente Southern California primary care clinics, with 13 serving as intervention clinics and 13 as usual care clinics. Patients 65 years and older with memory concerns (n ~ 180,000) receiving care at the 26 clinics will be included in the analyses. Primary care clinics are provided the following practice supports as part of the TabCAT-BHA intervention: brief education and training on neurocognitive disorders and study workflows; digital tools to assess cognitive function and support clinician decision making and documentation; and registered nurse support during the work-up and post-diagnosis periods for primary care providers, patients, and families. The intervention was adapted based on engagement with multiple levels of clinical and operational leaders in the healthcare system. Effectiveness outcomes include rates of cognitive impairment diagnosis in primary care and rates of completed standardized cognitive assessments and specialist referrals with incident diagnoses. Implementation outcomes include acceptability-appropriateness-feasibility, adoption, and fidelity. We identified seven themes organized by system-, provider-, and patient-level domains that were used to adapt the TabCAT-BHA intervention. Accordingly, changes were made to the provider education, diagnostic work-up, and post-diagnostic support. Results will be reported in fall of 2027. Our engagement with multiple primary and specialty care clinical and operational leaders to adapt the TabCAT-BHA intervention to these primary care clinics has informed the protocol to evaluate the intervention's effectiveness for improving the detection of cognitive impairment, including dementia, in an integrated healthcare system. Clinicaltrials.gov: NCT06090578 (registered 10/24/23).

Sections du résumé

BACKGROUND BACKGROUND
Cognitive impairment and dementia are frequently under-recognized. Health system strategies anchored in primary care are essential to address gaps in timely, comprehensive diagnosis. The goal of this paper is to describe the adaptation of a tablet-based brain health assessment (TabCAT-BHA) intervention and the study protocol to test its effectiveness in improving the detection of cognitive impairment, including dementia.
METHODS METHODS
This mixed-methods, pragmatic, cluster randomized, hybrid effectiveness-implementation trial is being conducted in two 18-month waves with 26 Kaiser Permanente Southern California primary care clinics, with 13 serving as intervention clinics and 13 as usual care clinics. Patients 65 years and older with memory concerns (n ~ 180,000) receiving care at the 26 clinics will be included in the analyses. Primary care clinics are provided the following practice supports as part of the TabCAT-BHA intervention: brief education and training on neurocognitive disorders and study workflows; digital tools to assess cognitive function and support clinician decision making and documentation; and registered nurse support during the work-up and post-diagnosis periods for primary care providers, patients, and families. The intervention was adapted based on engagement with multiple levels of clinical and operational leaders in the healthcare system. Effectiveness outcomes include rates of cognitive impairment diagnosis in primary care and rates of completed standardized cognitive assessments and specialist referrals with incident diagnoses. Implementation outcomes include acceptability-appropriateness-feasibility, adoption, and fidelity.
RESULTS RESULTS
We identified seven themes organized by system-, provider-, and patient-level domains that were used to adapt the TabCAT-BHA intervention. Accordingly, changes were made to the provider education, diagnostic work-up, and post-diagnostic support. Results will be reported in fall of 2027.
CONCLUSIONS CONCLUSIONS
Our engagement with multiple primary and specialty care clinical and operational leaders to adapt the TabCAT-BHA intervention to these primary care clinics has informed the protocol to evaluate the intervention's effectiveness for improving the detection of cognitive impairment, including dementia, in an integrated healthcare system.
TRIAL REGISTATION BACKGROUND
Clinicaltrials.gov: NCT06090578 (registered 10/24/23).

Identifiants

pubmed: 39107706
doi: 10.1186/s12875-024-02544-9
pii: 10.1186/s12875-024-02544-9
doi:

Banques de données

ClinicalTrials.gov
['NCT06090578']

Types de publication

Journal Article Clinical Trial Protocol

Langues

eng

Sous-ensembles de citation

IM

Pagination

286

Subventions

Organisme : NINDS NIH HHS
ID : U01NS128913
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS128913
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS128913
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS128913
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS128913
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS128913
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS128913
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS128913
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS128913
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS128913
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS128913
Pays : United States
Organisme : NINDS NIH HHS
ID : U01NS128913
Pays : United States

Informations de copyright

© 2024. The Author(s).

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Auteurs

Alissa Bernstein Sideman (AB)

Department of Neurology, University of California, San Francisco, San Francisco, USA.
Global Brain Health Institute, University of California, San Francisco, San Francisco, USA.

Huong Q Nguyen (HQ)

Department of Research and Evaluation, Kaiser Permanente Southern California, Southern California Permanente Medical Group, 100 S. Los Robles Avenue, 2nd Floor, Pasadena, CA, 91101, USA. huong.q2.nguyen@kp.org.
Department of Health Systems Science, Kaiser Permanente Bernard J Tyson School of Medicine, Pasadena, USA. huong.q2.nguyen@kp.org.

Annette Langer-Gould (A)

Department of Research and Evaluation, Kaiser Permanente Southern California, Southern California Permanente Medical Group, 100 S. Los Robles Avenue, 2nd Floor, Pasadena, CA, 91101, USA.
Department of Health Systems Science, Kaiser Permanente Bernard J Tyson School of Medicine, Pasadena, USA.
Department of Neurology, Los Angeles Medical Center, Southern California Permanente Medical Group, Los Angeles, USA.

Eric A Lee (EA)

Department of Clinical Sciences, Kaiser Permanente Bernard J Tyson School of Medicine, Pasadena, USA.
Department of Internal Medicine, Southern California Permanente Medical Group, West Los Angeles Medical Center, Los Angeles, USA.

Soo Borson (S)

Department of Research and Evaluation, Kaiser Permanente Southern California, Southern California Permanente Medical Group, 100 S. Los Robles Avenue, 2nd Floor, Pasadena, CA, 91101, USA.
Department of Family Medicine, University of Southern California Keck School of Medicine, Los Angeles, USA.

Ernest Shen (E)

Department of Research and Evaluation, Kaiser Permanente Southern California, Southern California Permanente Medical Group, 100 S. Los Robles Avenue, 2nd Floor, Pasadena, CA, 91101, USA.

Elena Tsoy (E)

Department of Neurology, University of California, San Francisco, San Francisco, USA.
Global Brain Health Institute, University of California, San Francisco, San Francisco, USA.

Mayra Macias (M)

Department of Research and Evaluation, Kaiser Permanente Southern California, Southern California Permanente Medical Group, 100 S. Los Robles Avenue, 2nd Floor, Pasadena, CA, 91101, USA.

Collette Goode (C)

Department of Neurology, University of California, San Francisco, San Francisco, USA.

Katherine Rankin (K)

Department of Neurology, University of California, San Francisco, San Francisco, USA.

Joel Kramer (J)

Department of Neurology, University of California, San Francisco, San Francisco, USA.

Katherine L Possin (KL)

Department of Neurology, University of California, San Francisco, San Francisco, USA.
Global Brain Health Institute, University of California, San Francisco, San Francisco, USA.

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