Evidence map›Paper›PMID 24220233›Full record

ArticleJournal of medical Internet research2013

Patients' reported reasons for non-use of an internet-based patient-provider communication service: qualitative interview study.

Cecilie Varsi, Deede Gammon, Torunn Wibe, Cornelia M Ruland

Registry-linked trialAbstract read
In one paragraph

Article in Journal of medical Internet research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00971139 (Implementing Online Patient-Provider Communication Into Clinical Practice), which is not on this map. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
–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.

NCT00971139 nacompletednot on this map

Implementing Online Patient-Provider Communication Into Clinical Practice: Implementation Research

TypeinterventionalSponsorOslo University HospitalRan2009 to 2013Enrolled199ConditionsCancer, Injury of Liver, DiabetesArmsAccess to an OPPC service
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  20. eHealth patient-provider communication in the United States: interest, inequalities, and predictors.Journal of the American Medical Informatics Association : JAMIA · 2017
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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

4 authors.

Cecilie VarsiCenter for Shared Decision Making and Collaborative Care Research, Oslo University Hospital, Oslo, Norway. cecilie.varsi@rr-research.no.ORCID 0000-0001-5257-7993
Deede Gammon
Torunn Wibe
Cornelia M Ruland

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe adoption of Internet-based patient-provider communication services (IPPC) in health care has been slow. Patients want electronic communication, and the quality of health care can be improved by offering such IPPCs. However, the rate of enrollment in such services remains low, and the reasons for this are unclear. Knowledge about the barriers to use is valuable during implementation of IPPCs in the health care services, and it can help timing, targeting, and tailoring IPPCs to different groups of patients.

objectiveThe goal of our study was to investigate patients' views of an IPPC that they could use from home to pose questions to nurses and physicians at their treatment facility, and their reported reasons for non-use of the service.

methodsThis qualitative study was based on individual interviews with 22 patients who signed up for, but did not use, the IPPC.

resultsPatients appreciated the availability and the possibility of using the IPPC as needed, even if they did not use it. Their reported reasons for not using the IPPC fell into three main categories: (1) they felt that they did not need the IPPC and had sufficient access to information elsewhere, (2) they preferred other types of communication such as telephone or face-to-face contact, or (3) they were hindered by IPPC attributes such as login problems.

conclusionsPatients were satisfied with having the opportunity to send messages to health care providers through an IPPC, even if they did not use the service. IPPCs should be offered to the patients at an appropriate time in the illness trajectory, both when they need the service and when they are receptive to information about the service. A live demonstration of the IPPC at the point of enrollment might have increased its use.

trial registrationClinicalTrials.gov NCT00971139; http://clinicaltrial.gov/ct2/show/NCT00971139 (Archived by WebCite at http://www.webcitation.org/6KlOiYJrW).

Indexed as

Professional-Patient RelationsAdultAgedFemaleHumansInternetInterviews as TopicMaleMiddle AgedPatientsPrivacycommunicationemailInternetinterviews as topicpatient dropoutspatient non-usepatient preferenceprofessional-patient relationsqualitative research

Identifiers

PMID24220233
PMCPMC3841351

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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.