Evidence map›Paper›PMID 37620273›Full record

ArticleBMJ open2023

Evaluation of the efficacy and safety of an integrated telerehabilitation platform for home-based cardiac REHABilitation in patients with heart failure (E-REHAB): protocol for a randomised controlled trial.

Misato Chimura, Shinji Koba, Yasushi Sakata, Takayuki Ise, Hiroyuki Miura, Ryosuke Murai, Hiroshi Suzuki, Emi Maekawa, Keisuke Kida, Koki Matsuo and 11 more

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
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

21 authors at 18 institutions in 1 country.

Misato ChimuraDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Suita, Japan.ORCID 0000-0003-3674-9171
Shinji KobaDepartment of Medicine, Division of Cardiology, Showa University School of Medicine, Tokyo, Japan.
Yasushi SakataDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Suita, Japan sakata.yasushi.med@osaka-u.ac.jp.
Takayuki IseDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
Hiroyuki MiuraDepartment of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan.ORCID 0000-0002-1301-3906
Ryosuke MuraiDepartment of Cardiovascular Medicine, Kobe City Medical Center General Hospital, Kobe, Japan.
Hiroshi SuzukiDepartment of Cardiology, Showa University Fujigaoka Rehabilitation Hospital, Yokohama, Japan.
Emi MaekawaDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Keisuke KidaDivision of Cardiology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
Koki MatsuoDivision of Cardiovascular Medicine, Department of Internal Medicine, Hyogo Prefectural Harima-Himeji General Medical Center, Himeji, Japan.
Hirokazu KondoDepartment of Cardiology, Tenri Hospital, Tenri, Japan.
Kensuke TakabayashiDepartment of Cardiology, Hirakata Kosai Hospital, Hirakata, Japan.ORCID 0000-0002-5805-9879
Wataru FujimotoDepartment of Cardiology, Hyogo Prefectural Awaji Medical Center, Sumoto, Japan.
Yuichi TamuraDepartment of Cardiology, International University of Health and Welfare Mita Hospital, Tokyo, Japan.
Shunsuke ImaiDepartment of Cardiology, Shinrakuen Hospital, Niigata, Japan.
Shin-Ichiro MiuraDepartment of Cardiology, Fukuoka University School of Medicine, Fukuoka, Japan.
Hideki OriguchiDepartment of Cardiology, Japan Community Hearlthcare Organization, Kyushu Hospital, Kitakyushu, Japan.
Akiko GodaDepartment of Cardiovascular Medicine, Nishinomiya Watanabe Cardiovascular Cerebral Center, Nishinomiya, Japan.
Ryotaro SaitaDepartment of Medical Innovation, Osaka University Hospital, Suita, Japan.ORCID 0000-0001-8732-7310
Atsushi KikuchiDivision of Cardiology, Osaka General Medical Center, Osaka, Japan.
Tatsunori TaniguchiDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Suita, Japan.
The University of Osaka · JPFukuoka University · JPHimeji Medical Center · JPHyogo Brain and Heart Center · JPHyogo Prefectural Awaji Medical Center · JPKitasato University · JPKobe City Medical Center General Hospital · JPKyushu Hospital · JPMita Hospital · JPNational Cerebral and Cardiovascular Center · JPOsaka Prefectural Medical Center · JPOsaka University Hospital · JPShinrakuen Hospital · JPShowa University · JPShowa University Fujigaoka Hospital · JPSt. Marianna University School of Medicine · JPTenri Hospital · JPTokushima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCardiac rehabilitation (CR) is strongly recommended as a medical treatment to improve the prognosis and quality of life of patients with heart failure (HF); however, participation rates in CR are low compared with other evidence-based treatments. One reason for this is the geographical distance between patients' homes and hospitals. To address this issue, we developed an integrated telerehabilitation platform, RH-01, for home-based CR. We hypothesised that using the RH-01 platform for home-based CR would demonstrate non-inferiority compared with traditional centre-based CR. METHODS AND ANALYSIS: The E-REHAB trial aims to evaluate the efficacy and safety of RH-01 for home-based CR compared with traditional centre-based CR for patients with HF. This clinical trial will be conducted under a prospective, randomised, controlled and non-inferiority design with a primary focus on HF patients. Further, to assess the generalisability of the results in HF to other cardiovascular disease (CVD), the study will also include patients with other CVDs. The trial will enrol 108 patients with HF and 20 patients with other CVD. Eligible HF patients will be randomly assigned to either traditional centre-based CR or home-based CR in a 1:1 fashion. Patients with other CVDs will not be randomised, as safety assessment will be the primary focus. The intervention group will receive a 12-week programme conducted two or three times per week consisting of a remotely supervised home-based CR programme using RH-01, while the control group will receive a traditional centre-based CR programme. The primary endpoint of this trial is change in 6 min walk distance. ETHICS AND DISSEMINATION: The conduct of the study has been approved by an institutional review board at each participating site, and all patients will provide written informed consent before entry. The report of the study will be disseminated via scientific fora, including peer-reviewed publications and presentations at conferences. TRIAL REGISTRATION NUMBER: jRCT:2052200064.

Indexed as

Cardiac RehabilitationCardiovascular DiseasesHeart FailureTelerehabilitationHumansProspective StudiesQuality of LifeRandomized Controlled Trials as Topicheart failurerehabilitation medicinetelemedicine

Identifiers

PMID37620273
PMCPMC10450078
OpenAlexW4386125457

What OpenQuestion holds

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LicenceCC BY-NC
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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.