Evidence map›Paper›PMID 35544134›Full record

ArticleJAMA network open2022

Application of Patient-Reported Outcome Measurements in Clinical Trials in China.

Hui Zhou, Mi Yao, Xiaodan Gu, Mingrui Liu, Ruifeng Zeng, Qin Li, Tingjia Chen, Wen He, Xiao Chen, Gang Yuan

Abstract read
In one paragraph

Article in JAMA network open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing 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.

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

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

  1. Pooled it
  2. Differences and common ground in the frameworks of health-related quality of life in traditional Chinese medicine and modern medicine: a systematic review.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Hui ZhouPhase I Clinical Trial Center, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Mi YaoInstitute of Applied Health Research, University of Birmingham, Birmingham, United Kingdom.
Xiaodan GuPhase I Clinical Trial Center, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Mingrui LiuSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.
Ruifeng ZengPhase I Clinical Trial Center, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Qin LiDepartment of Geriatrics, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Tingjia ChenHealthcare Center, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Wen HeDepartment of Geriatrics, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xiao ChenDepartment of Pharmacy, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Gang YuanPhase I Clinical Trial Center, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Regulatory authorities, industry peers, and international health policies have emphasized the value of assessing patient-reported outcomes (PROs) in clinical studies. Despite the increase in the number of clinical studies in the last decade in China, little is known about the extent of the use of PROs. Objective: To evaluate the application and characteristics of PRO instruments as primary and secondary outcomes in randomized clinical trials in China. Design, Setting, and Participants: A cross-sectional study of interventional clinical trials conducted in China from January 1, 2010, to December 31, 2020, was performed. Data obtained from the Chinese Clinical Trial Registry and ClinicalTrials.gov databases were evaluated. Main Outcomes and Measures: Trials were categorized according to those that (1) precisely listed PRO tools as outcomes, (2) mentioned patient subjective feelings in outcomes but did not clarify which tools were used for assessment, and (3) did not mention any PRO measurements. Data on study phase, setting, participant age, and sex were extracted from trials that considered patient feelings, along with the target diseases and names of the PRO tools. Results: Among a total of 34 033 trials, 6915 (20.3%) listed the explicit PRO instruments used and 3178 (9.3%) included PRO in their outcomes but did not include the names of the assessment tools. From more than 32 million people included in the registered trials, data on 1.5 million (4.7%) patients were scientifically collected by PRO instruments, and subjective feelings were assessed for 693 867 (2.1%) participants. Pain (16.8%), cancer (15.6%), and musculoskeletal symptoms (13.3%) were the most common conditions for which PROs were precisely collected by tools. The most common tools for PRO measurements were the visual analog scale, Short-Form 36, and Hamilton Depression Scale. Conclusions and Relevance: In this cross-sectional study, the use of PROs increased during the study period in clinical trials conducted in China. However, patient opinion appears to still be rarely measured. The application of PRO is geographically unevenly distributed. Development of PRO instruments, especially those suitable for the Chinese population, may be useful. Further expansion of PROs with respect to the scope of diseases is needed to avoid missing important data.

Indexed as

Clinical Trials as TopicPatient Reported Outcome MeasuresChinaCross-Sectional StudiesDatabases, FactualHumansNeoplasms

Identifiers

PMID35544134
PMCPMC9096600

What OpenQuestion holds

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Registered trials

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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.