Evidence map›Paper›PMID 36351726›Full record

ArticleBMJ open2022

Test reliability and comparability of paper and Chinese electronic version of the western Ontario and McMaster University osteoarthritis index: protocol for a randomised controlled clinical trial.

Yujie Zhang, Ye Zhao, Kaoqiang Liu, Yongli Chai, Fen Lin, Hongsheng Zhan, Yuxin Zheng, Weian Yuan

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
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

8 authors at 1 institution in 1 country.

Yujie ZhangShuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, ShangHai, 201203, China.ORCID 0000-0003-1588-8842
Ye ZhaoShuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, ShangHai, 201203, China.
Kaoqiang LiuShuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, ShangHai, 201203, China.
Yongli ChaiShuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, ShangHai, 201203, China.
Fen LinShanghai Jsure Health Co., Ltd, Shanghai, China.
Hongsheng ZhanShuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, ShangHai, 201203, China weian_1980@163.com 13918449223@139.com sg_zyx1728@126.com.
Yuxin ZhengShuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, ShangHai, 201203, China weian_1980@163.com 13918449223@139.com sg_zyx1728@126.com.
Weian YuanShuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, ShangHai, 201203, China weian_1980@163.com 13918449223@139.com sg_zyx1728@126.com.
Shanghai University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe Western Ontario and McMaster University osteoarthritis index (WOMAC) is the most commonly used indicator of disease-specific outcome in knee osteoarthritis for its convenience and reliability. It has two formats the paper-based WOMAC (p-WOMAC) and the electronic WOMAC (e-WOMAC). In China, the p-WOMAC has been widely used though e-WOMAC is yet untested. This study aims to test whether e-WOMAC is consistent with the p-WOMAC before and after the intervention. METHODS AND ANALYSIS: A total of 70 patients from Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine will be randomly assigned in two groups, named, group A and group B. This study is divided into three stages. In the first stage, patients in group A will be evaluated first by p-WOMAC and then by e-WOMAC. Patients in group B will be evaluated by e-WOMAC and then by p-WOMAC. In the second stage of the study, drug interventions will be implemented. 200 mg celecoxib will be administered orally once a day starting from the second day of enrolment for a period of 21 days. In the third stage, postintervention evaluation will be conducted after administration. Patients in group A will be evaluated first by e-WOMAC and then by p-WOMAC. Patients in group B will be evaluated first by p-WOMAC and then by e-WOMAC. In order to avoid the possible bias because of patients' potential memory, e-WOMAC and p-WOMAC will be taken for each patient at 15 min apart. The primary outcome of the study is the mean score difference in WOMAC, and the secondary outcomes are the score differences in WOMAC subscales: pain, stiffness and physical function. ETHICS AND DISSEMINATION: The protocol has been approved by the Independent Review Board of SGH (approval number: 2020-814-21-01). The results of the trial will be submitted for publication in a peer-reviewed journal. TRIAL REGISTRATION NUMBER: ChiCTR2100050914.

Indexed as

Osteoarthritis, KneeChinaElectronicsHumansOntarioRandomized Controlled Trials as TopicReproducibility of ResultsTreatment OutcomeUniversitiesInformation technologyMusculoskeletal disordersPRIMARY CARE

Identifiers

PMID36351726
PMCPMC9644355
OpenAlexW4308658842

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.