Evidence map›Paper›PMID 34289996›Full record

Trial reportBMJ (Clinical research ed.)2021

Real time remote symptom monitoring during chemotherapy for cancer: European multicentre randomised controlled trial (eSMART).

Roma Maguire, Lisa McCann, Grigorios Kotronoulas, Nora Kearney, Emma Ream, Jo Armes, Elisabeth Patiraki, Eileen Furlong, Patricia Fox, Alexander Gaiger and 16 more

Erratum issued 2 registry-linked trialsOpen access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in BMJ (Clinical research ed.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 2 registered trials, which are not on this map. Cited by 151 papers, 16 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
151citing papers in PubMed, 16 pooled it
14.8field-weighted citation impact, top 1% 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.

NCT02356081 nacompletednot on this map

eSMART: Randomised Controlled Trial to Evaluate Electronic Symptom Management Using the Advanced Symptom Management System (ASyMS) Remote Technology for Patients With Cancers

TypeinterventionalSponsorLouise McKeanRan2015 to 2019Enrolled829ConditionsCancerArmsASyMS intervention Group
NCT05946070 nacompletednot on this mapstarted 2023, after this paper: background citation

Effectiveness of Mobile Based Monitoring System in the Management of Chemotherapy-Related Symptoms

TypeinterventionalSponsorIstanbul University - CerrahpasaRan2023 to 2024Enrolled199ConditionsCancer, Chemotherapeutic Toxicity, Mobile ApplicationsArmsONKOSIS
3 · Its place in the literature

Who cites it

151 citing papers in PubMed, 16 syntheses or guidelines pooled it, 234 citations in OpenAlex.

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  3. Effectiveness of eHealth interventions in long-term follow-up care for breast and gynecological cancer survivors: a systematic review.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
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  11. Effectiveness of ePRO-based symptom management for cancer patients: a systematic review and meta-analysis of randomized controlled studies.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2024
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  14. Interactive digital tools to support empowerment of people with cancer: a systematic literature review.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2024
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  20. Effectiveness of mobile-based monitoring system (ONKOSIS) in the management of chemotherapy-related symptoms: a randomized controlled trial.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
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91 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 14 institutions in 7 countries.

Roma MaguireComputer and Information Sciences, University of Strathclyde, Glasgow, UK Roma.maguire@strath.ac.uk.ORCID 0000-0001-7935-3447
Lisa McCannComputer and Information Sciences, University of Strathclyde, Glasgow, UK.
Grigorios KotronoulasSchool of Medicine, Dentistry and Nursing, University of Glasgow, Glasgow, UK.
Nora KearneyLeven, UK.
Emma ReamUniversity of Surrey, School of Health Sciences, Guildford, UK.
Jo ArmesUniversity of Surrey, School of Health Sciences, Guildford, UK.
Elisabeth PatirakiNational and Kapodistrian University of Athens School of Health Sciences, Athens, Greece.
Eileen FurlongSchool of Nursing, Midwifery and Health Systems, University College Dublin, Dublin, Ireland.
Patricia FoxSchool of Nursing, Midwifery and Health Systems, University College Dublin, Dublin, Ireland.
Alexander GaigerDepartment of Internal Medicine 1, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
Paul McCroneDepartment of Health Services and Population Research, King's College London Institute of Psychiatry Psychology and Neuroscience, London, UK.
Geir BergDepartment of Health Sciences, NTNU, Gjøvik, Norway.
Christine MiaskowskiUniversity of California San Francisco, San Francisco, CA, USA.
Antonella CardoneEuropean Cancer Patient Coalition, Brussels, Belgium.
Dawn OrrNHS 24, Glasgow, UK.
Adrian FlowerdayDocobo Limited, Leatherhead, UK.
Stylianos KatsaragakisNational and Kapodistrian University of Athens School of Health Sciences, Athens, Greece.
Andrew DarleySchool of Medicine, University College Dublin, Dublin, Ireland.
Simone LubowitzkiDepartment of Internal Medicine 1, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
Jenny HarrisUniversity of Surrey, School of Health Sciences, Guildford, UK.
Simon SkeneSurrey Clinical Trials Unit, University of Surrey, Guildford, UK.
Morven MillerComputer and Information Sciences, University of Strathclyde, Glasgow, UK.
Margaret MooreComputer and Information Sciences, University of Strathclyde, Glasgow, UK.
Liane LewisJohnson and Johnson Medical, Norderstedt, Germany.
Nicosha DeSouzaPopulation Health and Genomics, Medical School, University of Dundee, Dundee, UK.
Peter T DonnanPopulation Health and Genomics, Medical School, University of Dundee, Dundee, UK.
University of Strathclyde · GBUniversity of Surrey · GBUniversity College Dublin · IEMedical University of Vienna · ATNational and Kapodistrian University of Athens · GRUniversity of Dundee · GBDocobo (United Kingdom) · GBEuropean CanCer Organisation · BEJohnson & Johnson (Germany) · DEKing's College London · GBNHS Greater Glasgow and Clyde · GBUniversity of California, San Francisco · USUniversity of Glasgow · GBVale of Leven District General Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate effects of remote monitoring of adjuvant chemotherapy related side effects via the Advanced Symptom Management System (ASyMS) on symptom burden, quality of life, supportive care needs, anxiety, self-efficacy, and work limitations.

designMulticentre, repeated measures, parallel group, evaluator masked, stratified randomised controlled trial.

settingTwelve cancer centres in Austria, Greece, Norway, Republic of Ireland, and UK.

participants829 patients with non-metastatic breast cancer, colorectal cancer, Hodgkin's disease, or non-Hodgkin's lymphoma receiving first line adjuvant chemotherapy or chemotherapy for the first time in five years.

interventionPatients were randomised to ASyMS (intervention; n=415) or standard care (control; n=414) over six cycles of chemotherapy.

main outcome measuresThe primary outcome was symptom burden (Memorial Symptom Assessment Scale; MSAS). Secondary outcomes were health related quality of life (Functional Assessment of Cancer Therapy-General; FACT-G), Supportive Care Needs Survey Short-Form (SCNS-SF34), State-Trait Anxiety Inventory-Revised (STAI-R), Communication and Attitudinal Self-Efficacy scale for cancer (CASE-Cancer), and work limitations questionnaire (WLQ).

resultsFor the intervention group, symptom burden remained at pre-chemotherapy treatment levels, whereas controls reported an increase from cycle 1 onwards (least squares absolute mean difference -0.15, 95% confidence interval -0.19 to -0.12; P<0.001; Cohen's D effect size=0.5). Analysis of MSAS sub-domains indicated significant reductions in favour of ASyMS for global distress index (-0.21, -0.27 to -0.16; P<0.001), psychological symptoms (-0.16, -0.23 to -0.10; P<0.001), and physical symptoms (-0.21, -0.26 to -0.17; P<0.001). FACT-G scores were higher in the intervention group across all cycles (mean difference 4.06, 95% confidence interval 2.65 to 5.46; P<0.001), whereas mean scores for STAI-R trait (-1.15, -1.90 to -0.41; P=0.003) and STAI-R state anxiety (-1.13, -2.06 to -0.20; P=0.02) were lower. CASE-Cancer scores were higher in the intervention group (mean difference 0.81, 0.19 to 1.43; P=0.01), and most SCNS-SF34 domains were lower, including sexuality needs (-1.56, -3.11 to -0.01; P<0.05), patient care and support needs (-1.74, -3.31 to -0.16; P=0.03), and physical and daily living needs (-2.8, -5.0 to -0.6; P=0.01). Other SCNS-SF34 domains and WLQ were not significantly different. Safety of ASyMS was satisfactory. Neutropenic events were higher in the intervention group.

conclusionsSignificant reduction in symptom burden supports the use of ASyMS for remote symptom monitoring in cancer care. A "medium" Cohen's effect size of 0.5 showed a sizable, positive clinical effect of ASyMS on patients' symptom experiences. Remote monitoring systems will be vital for future services, particularly with blended models of care delivery arising from the covid-19 pandemic.

trial registrationClinicaltrials.gov NCT02356081.

Indexed as

Cell PhoneQuality of LifeAdultAgedAntineoplastic Combined Chemotherapy ProtocolsAustriaBreast NeoplasmsChemotherapy, AdjuvantColorectal NeoplasmsDrug-Related Side Effects and Adverse ReactionsFemaleGreeceHodgkin DiseaseHumansIrelandLymphoma, Non-Hodgkin

Identifiers

PMID34289996
PMCPMC8293749
OpenAlexW3183953444

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.