Evidence map›Paper›PMID 33541402›Full record

ArticleTrials2021

Barriers impacting the POINT pragmatic trial: the unavoidable overlap between research and intervention procedures in "real-world" research.

Allyson L Dir, Dennis P Watson, Matthew Zhiss, Lisa Taylor, Bethany C Bray, Alan McGuire

Open access · goldAbstract read
In one paragraph

Article in Trials, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 14% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

6 authors at 5 institutions in 1 country.

Allyson L DirDepartment of Psychiatry, Indiana University School of Medicine, 410 W 10th Street, Suite 2000, Indianapolis, IN, 46202, USA.
Dennis P WatsonLighthouse Institute, Chestnut Health Systems, 221 W Walton St., Chicago, IL, 60610, USA. dpwatson@chestnut.org.ORCID http://orcid.org/0000-0001-7208-5160
Matthew ZhissSchool of Social Work, Indiana University Purdue University Indianapolis, 902 West New York Street, Indianapolis, IN, 46202, USA.
Lisa TaylorCenter for Dissemination and Implementation Science, Department of Medicine, College of Medicine, University of Illinois at Chicago, 818 S. Wolcott, Chicago, IL, 60612, USA.
Bethany C BrayCenter for Dissemination and Implementation Science, Department of Medicine, College of Medicine, University of Illinois at Chicago, 818 S. Wolcott, Chicago, IL, 60612, USA.
Alan McGuireDepartment of Psychology, Indiana University Purdue University Indianapolis, 402 N. Blackford St., Indianapolis, IN, 46202, USA.
University of Illinois Chicago · USChestnut Health Systems · USIndiana University School of MedicineRichard L. Roudebush VA Medical Center · USUniversity of Indianapolis · US

Funding

Project POINT: Effectiveness and Scalability of an Overdose Survivor InterventionR33DA045850 · NIDA · INDIANA UNIVERSITY INDIANAPOLIS · PI MCGUIRE, ALAN BENJAMIN, WATSON, DENNIS PAUL · 2018 to 2020
$1.9M
Project POINT: Effectiveness and Scalability of an Overdose Survivor InterventionR21DA045850 · NIDA · INDIANA UNIVERSITY INDIANAPOLIS · PI WATSON, DENNIS PAUL · 2017 to 2017
$288k
NIDA NIH HHS R21 DA045850NIDA NIH HHS R21DA045850NIDA NIH HHS R33 DA045850NIDA NIH HHS R33DA045850
6 · The paper itself

Abstract

backgroundThis manuscript provides a research update to the ongoing pragmatic trial of Project POINT (Planned Outreach, Intervention, Naloxone, and Treatment), an emergency department-based peer recovery coaching intervention for linking patients with opioid use disorder to evidence-based treatment. The research team has encountered a number of challenges related to the "real-world" study setting since the trial began. Using an implementation science lens, we sought to identify and describe barriers impacting both the intervention and research protocols of the POINT study, which are often intertwined in pragmatic trials due to the focus on external validity.

methodQualitative data were collected from 3 peer recovery coaches, 2 peer recovery coach supervisors, and 3 members of the research team. Questions and deductive qualitative analysis were guided by the Consolidated Framework for Implementation Research (CFIR).

resultsNine unique barriers were noted, with 5 of these barriers impacting intervention and research protocol implementation simultaneously. These simultaneous barriers were timing of intervention delivery, ineffective communication with emergency department staff, lack of privacy in the emergency department, the fast-paced emergency department setting, and patient's limited resources. Together, these barriers represent the intervention characteristics, inner setting, and outer setting domains of the CFIR.

conclusionResults highlight the utility of employing an implementation science framework to assess implementation issues in pragmatic trials and how this approach might be used as a quality assurance mechanism given the considerable overlap that exists between research and intervention protocols in real-world trial settings. Previously undocumented changes to the trial design that have been made as a result of the identified barriers are discussed.

Indexed as

NaloxoneOpioid-Related DisordersCommunicationEmergency Service, HospitalHumansLongitudinal StudiesNaloxoneConsolidated Framework for Implementation ResearchEmergency departmentExternal validityImplementationMedication for opioid use disorderOpioid use disorderOverdosePragmatic trial

Identifiers

PMID33541402
PMCPMC7859893
OpenAlexW3128527595

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.