Evidence map›Paper›PMID 31888732›Full record

ArticleTrials2019

INtervention for Cognitive Reserve Enhancement in delaying the onset of Alzheimer's Symptomatic Expression (INCREASE), a randomized controlled trial: rationale, study design, and protocol.

Daniela C Moga, Brooke F Beech, Erin L Abner, Frederick A Schmitt, Riham H El Khouli, Ashley I Martinez, Lynne Eckmann, Mark Huffmyer, Rosmy George, Gregory A Jicha

Registry-linked trialOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02849639 (INtervention for Cognitive Reserve Enhancement in Delaying the Onset of Alzheimer's Symptomatic Expression), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02849639 early_phase1completednot on this map

INtervention for Cognitive Reserve Enhancement in Delaying the Onset of Alzheimer's Symptomatic Expression: The INCREASE Study

TypeinterventionalSponsorDaniela MogaRan2017 to 2021Enrolled90ConditionsAlzheimer's Disease, DementiaArmsPlacebo, Medication Therapy Management (MTM), Scopolamine patch
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Evaluation of anticholinergic burden in elderly outpatients and the risk factors.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
    Article
  7. Review
  8. Article
  9. Article
  10. Attitudes toward deprescribing in a middle-aged health disparities population.Research in social & administrative pharmacy : RSAP · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Daniela C MogaDepartment of Pharmacy Practice and Science, College of Pharmacy, University of Kentucky, Lexington, KY, USA. daniela.moga@uky.edu.ORCID http://orcid.org/0000-0002-3648-8197
Brooke F BeechSanders-Brown Center on Aging, Lexington, KY, USA.
Erin L AbnerDepartment of Epidemiology, College of Public Health, University of Kentucky, Lexington, KY, USA.
Frederick A SchmittSanders-Brown Center on Aging, Lexington, KY, USA.
Riham H El KhouliDepartment of Radiology, College of Medicine, University of Kentucky, Lexington, KY, USA.
Ashley I MartinezDepartment of Pharmacy Practice and Science, College of Pharmacy, University of Kentucky, Lexington, KY, USA.
Lynne EckmannPRO2RX LLC Pharmacy Consulting Services, Lexington, KY, USA.
Mark HuffmyerDepartment of Pharmacy Practice and Science, College of Pharmacy, University of Kentucky, Lexington, KY, USA.
Rosmy GeorgeSanders-Brown Center on Aging, Lexington, KY, USA.
Gregory A JichaSanders-Brown Center on Aging, Lexington, KY, USA.
University of Kentucky · USUniversity of Kentucky HealthCare · US

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
University of Kentucky Alzheimer's Disease Core Center - Biomarker CoreP30AG028383 · NIA · UNIVERSITY OF KENTUCKY · PI SCHMITT, FREDERICK · 2006 to 2020
$23.3M
Kentucky Center for Clinical and Translational ScienceUL1TR000117 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$13.3M
INtervention for Cognitive Reserve Enhancement in delaying the onset of Alzheimer’s Symptomatic Expression: The INCREASE studyR01AG054130 · NIA · UNIVERSITY OF KENTUCKY · PI JICHA, GREGORY A, MOGA, DANIELA CLAUDIA · 2016 to 2020
$2.0M
NCATS NIH HHS UL1 TR000117NIA NIH HHS P30 AG028383NIA NIH HHS R01 AG054130
6 · The paper itself

Abstract

backgroundThe course of Alzheimer's disease (AD) includes a 10-20-year preclinical period with progressive accumulation of amyloid β (Aβ) plaques and neurofibrillary tangles in the absence of symptomatic cognitive or functional decline. The duration of this preclinical stage in part depends on the rate of pathologic progression, which is offset by compensatory mechanisms, referred to as cognitive reserve (CR). Comorbid medical conditions, psychosocial stressors, and inappropriate medication use may lower CR, hastening the onset of symptomatic AD. Here, we describe a randomized controlled trial (RCT) designed to test the efficacy of a medication therapy management (MTM) intervention to reduce inappropriate medication use, bolster cognitive reserve, and ultimately delay symptomatic AD. METHODS/

designOur study aims to enroll 90 non-demented community-dwelling adults ≥ 65 years of age. Participants will undergo positron emission tomography (PET) scans, measuring Aβ levels using standardized uptake value ratios (SUVr). Participants will be randomly assigned to MTM intervention or control, stratified by Aβ levels, and followed for 12 months via in-person and telephone visits. Outcomes of interest include: (1) medication appropriateness (measured with the Medication Appropriateness Index (MAI)); (2) scores from Trail Making Test B (TMTB), Montreal Cognitive Assessment (MoCA), and California Verbal Learning Test (CVLT); (3) perceived health status (measured with the SF-36). We will also evaluate pre- to post-intervention change in: (1) use of inappropriate medications as measured by MAI; 2) CR Change Score (CRCS), defined as the difference in scopolamine-challenged vs unchallenged cognitive scores at baseline and follow-up. Baseline Aβ SUVr will be used to examine the relative impact of preclinical AD (pAD) pathology on CRCS, as well as the interplay of amyloid burden with inappropriate medication use. DISCUSSION: This manuscript describes the protocol of INCREASE ("INtervention for Cognitive Reserve Enhancement in delaying the onset of Alzheimer's Symptomatic Expression"): a randomized controlled trial that investigates the impact of deprescribing inappropriate medications and optimizing medication regimens on potentially delaying the onset of symptomatic AD and AD-related dementias.

trial registrationClinicalTrials.gov, NCT02849639. Registered on 29 July 2016.

Indexed as

Cognitive ReserveIndependent LivingAgedAged, 80 and overAlzheimer DiseaseAmyloid beta-PeptidesCognitive DysfunctionComorbidityDisease ProgressionDrug-Related Side Effects and Adverse ReactionsEarly Medical InterventionFemaleFollow-Up StudiesHealth StatusHumansMaleAmyloid beta-PeptidesAlzheimer’s diseaseBeers criteriaCognitive reserveComprehensive medication reviewDementiaDeprescribingInappropriate medicationInterdisciplinaryMedication therapy managementPatient-centered

Identifiers

PMID31888732
PMCPMC6937673
OpenAlexW2998358053

What OpenQuestion holds

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LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.