Evidence map›Paper›PMID 27852237›Full record

ArticleBMC medical research methodology2016

Using cognitive pre-testing methods in the development of a new evidenced-based pressure ulcer risk assessment instrument.

S Coleman, J Nixon, J Keen, D Muir, L Wilson, E McGinnis, N Stubbs, C Dealey, E A Nelson

Abstract read
In one paragraph

Article in BMC medical research methodology, 2016. 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
–field-weighted citation impact
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.

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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

9 authors.

S ColemanLeeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK. medscole@leeds.ac.uk.
J NixonLeeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK.
J KeenLeeds Institute of Health Sciences, University of Leeds, Leeds, UK.
D MuirLeeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK.
L WilsonLeeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK.
E McGinnisLeeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK.
N StubbsWound Prevention and Management Service, Leeds Community Healthcare NHS Trust, Leeds, UK.
C DealeySchool of Health & Population Sciences, University of Birmingham, Birmingham, UK.
E A NelsonSchool of Healthcare, University of Leeds, Leeds, UK.

Funding

Department of Health RP-PG-0407-10056
6 · The paper itself

Abstract

backgroundVariation in development methods of Pressure Ulcer Risk Assessment Instruments has led to inconsistent inclusion of risk factors and concerns about content validity. A new evidenced-based Risk Assessment Instrument, the Pressure Ulcer Risk Primary Or Secondary Evaluation Tool - PURPOSE-T was developed as part of a National Institute for Health Research (NIHR) funded Pressure Ulcer Research Programme (PURPOSE: RP-PG-0407-10056). This paper reports the pre-test phase to assess and improve PURPOSE-T acceptability, usability and confirm content validity.

methodsA descriptive study incorporating cognitive pre-testing methods and integration of service user views was undertaken over 3 cycles comprising PURPOSE-T training, a focus group and one-to-one think-aloud interviews. Clinical nurses from 2 acute and 2 community NHS Trusts, were grouped according to job role. Focus group participants used 3 vignettes to complete PURPOSE-T assessments and then participated in the focus group. Think-aloud participants were interviewed during their completion of PURPOSE-T. After each pre-test cycle analysis was undertaken and adjustment/improvements made to PURPOSE-T in an iterative process. This incorporated the use of descriptive statistics for data completeness and decision rule compliance and directed content analysis for interview and focus group data. Data were collected April 2012-June 2012.

resultsThirty-four nurses participated in 3 pre-test cycles. Data from 3 focus groups, 12 think-aloud interviews incorporating 101 PURPOSE-T assessments led to changes to improve instrument content and design, flow and format, decision support and item-specific wording. Acceptability and usability were demonstrated by improved data completion and appropriate risk pathway allocation. The pre-test also confirmed content validity with clinical nurses.

conclusionsThe pre-test was an important step in the development of the preliminary PURPOSE-T and the methods used may have wider instrument development application. PURPOSE-T proposes a new approach to pressure ulcer risk assessment, incorporating a screening stage, the inclusion of skin status to distinguish between those who require primary prevention and those who require secondary prevention/treatment and the use of colour to support pathway allocation and decision making. Further clinical evaluation is planned to assess the reliability and validity of PURPOSE-T and it's impact on care processes and patient outcomes.

Indexed as

CognitionSurveys and QuestionnairesAdultEvidence-Based MedicineFemaleFocus GroupsHumansMaleMiddle AgedNurse's RolePressure UlcerReproducibility of ResultsRisk AssessmentRisk FactorsYoung AdultCognitive pre-testing methodsNursingPatient and Public Involvement (PPI)Pressure ulcerRisk assessmentTissue viability

Identifiers

PMID27852237
PMCPMC5112672

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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.