Evidence map›Paper›PMID 33234644›Full record

ArticleBMJ open2020

Improving the Safety and Continuity Of Medicines management at Transitions of care (ISCOMAT): protocol for a process evaluation of a cluster randomised control trial.

Catherine Powell, Liz Breen, Beth Fylan, Hanif Ismail, Sarah L Alderson, Chris P Gale, Peter Gardner, Amanda J Farrin, David P Alldred, ISCOMAT Programme Management Team

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Trial
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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

10 authors at 2 institutions in 1 country.

Catherine PowellSchool of Pharmacy and Medical Sciences, Faculty of Life Sciences, University of Bradford, Bradford, UK C.Powell2@bradford.ac.uk.ORCID 0000-0001-7590-0247
Liz BreenSchool of Pharmacy and Medical Sciences, Faculty of Life Sciences, University of Bradford, Bradford, UK.ORCID 0000-0001-5204-1187
Beth FylanSchool of Pharmacy and Medical Sciences, Faculty of Life Sciences, University of Bradford, Bradford, UK.ORCID 0000-0003-0599-4537
Hanif IsmailSchool of Pharmacy and Medical Sciences, Faculty of Life Sciences, University of Bradford, Bradford, UK.ORCID 0000-0002-7885-6648
Sarah L AldersonLeeds Institute of Health Sciences, University of Leeds, Leeds, UK.ORCID 0000-0002-5418-0495
Chris P GaleLeeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.ORCID 0000-0003-4732-382X
Peter GardnerSchool of Pharmacy and Medical Sciences, Faculty of Life Sciences, University of Bradford, Bradford, UK.ORCID 0000-0002-8799-0443
Amanda J FarrinClinical Trials Research Unit, University of Leeds, Leeds, UK.ORCID 0000-0002-2876-0584
David P AlldredWolfson Centre for Applied Health Research, Bradford, UK.ORCID 0000-0002-2525-4854
ISCOMAT Programme Management Team
University of Bradford · GBUniversity of Leeds · GB

Funding

Department of Health RP-PG-0514-20009
6 · The paper itself

Abstract

introductionA key priority for the UK National Health Service and patients is to ensure that medicines are used safely and effectively. However, medication changes are not always optimally communicated and implemented when patients transfer from hospital into community settings. Heart failure is a common reason for admission to hospital. Patients with heart failure have a high burden of morbidity, mortality and complex pharmacotherapeutic regimens. The Improving the Safety and Continuity Of Medicines management at Transitions of care programme comprises a cluster randomised controlled trial which will test the effectiveness of a complex behavioural intervention aimed at improving medications management at the interface between hospitals discharge and community care. We will conduct a rigorous process evaluation to inform interpretation of the trial findings, inform implementation of the intervention on a wider scale and aid dissemination of the intervention. METHODS AND ANALYSIS: The process evaluation will be conducted in six purposively selected intervention sites (ie, hospital trusts and associated community pharmacies) using a mixed-methods design. Fidelity and barriers/enablers of implementation of the Medicines at Transitions Intervention (MaTI) will be explored using observation, interviews (20 patients, 40 healthcare professionals), surveys and routine trial data collection on adherence to MaTI. A parallel mixed analysis will be applied. Qualitative data will be thematically analysed using Framework analysis and survey data will be analysed descriptively. Data will be synthesised, triangulated and mapped to the Consolidated Framework for Implementation Research where appropriate. The process evaluation commenced on June 2018 and is due to end on February 2021. ETHICS AND DISSEMINATION: Approved by Research Ethics Committee and the UK Health Research Authority REC: 18/YH/0017/IRAS: 231 431. Findings will be disseminated via academic and policy conferences, peer-reviewed publications and social media. TRIAL REGISTRATION NUMBER: ISRCTN66212970.

Indexed as

Heart FailureState MedicineHospitalizationHumansPatient DischargeRandomized Controlled Trials as TopicSurveys and Questionnairescardiologyclinical trialsheart failurestatistics & research methods

Identifiers

PMID33234644
PMCPMC7689064
OpenAlexW3108197210

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.