An international survey of physicians regarding clinical trials: a comparison between Kyoto University Hospital and Seoul National University Hospital.

Abstract:

BACKGROUND:International clinical trials are now rapidly expanding into Asia. However, the proportion of global trials is higher in South Korea compared to Japan despite implementation of similar governmental support in both countries. The difference in clinical trial environment might influence the respective physicians' attitudes and experience towards clinical trials. Therefore, we designed a questionnaire to explore how physicians conceive the issues surrounding clinical trials in both countries. METHODS:A questionnaire survey was conducted at Kyoto University Hospital (KUHP) and Seoul National University Hospital (SNUH) in 2008. The questionnaire consisted of 15 questions and 2 open-ended questions on broad key issues relating to clinical trials. RESULTS:The number of responders was 301 at KUHP and 398 at SNUH. Doctors with trial experience were 196 at KUHP and 150 at SNUH. Among them, 12% (24/196) at KUHP and 41% (61/150) at SUNH had global trial experience. Most respondents at both institutions viewed clinical trials favorably and thought that conducting clinical trials contributed to medical advances, which would ultimately lead to new and better treatments. The main reason raised as a hindrance to conducting clinical trials was the lack of personnel support and time. Doctors at both university hospitals thought that more clinical research coordinators were required to conduct clinical trials more efficiently. KUHP doctors were driven mainly by pure academic interest or for their desire to find new treatments, while obtaining credits for board certification and co-authorship on manuscripts also served as motivation factors for doctors at SNUH. CONCLUSIONS:Our results revealed that there might be two different approaches to increase clinical trial activity. One is a social level approach to establish clinical trial infrastructure providing sufficient clinical research professionals. The other is an individual level approach that would provide incentives to encourage doctors to participate in and conduct clinical trials.

journal_name

BMC Med Res Methodol

authors

Ito-Ihara T,Hong JH,Kim OJ,Sumi E,Kim SY,Tanaka S,Narita K,Hatta T,Choi EK,Choi KJ,Miyagawa T,Minami M,Murayama T,Yokode M

doi

10.1186/1471-2288-13-130

subject

Has Abstract

pub_date

2013-10-25 00:00:00

pages

130

issn

1471-2288

pii

1471-2288-13-130

journal_volume

13

pub_type

杂志文章
  • Pan-Canadian assessment of pandemic immunization data collection: study methodology.

    abstract:BACKGROUND:The collection of individual-level pandemic (H1N1) 2009 influenza immunization data was considered important to facilitate optimal vaccine delivery and accurate assessment of vaccine coverage. These data are also critical for research aimed at evaluating the new vaccine's safety and effectiveness. Systems us...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-10-51

    authors: Pereira JA,Quach S,Heidebrecht C,Foisy J,Quan S,Finkelstein M,Sikora CA,Bettinger JA,Buckeridge DL,McCarthy A,Deeks S,Kwong JC,Public Health Agency of Canada\/Canadian Institutes of Health Research Influenza Research Network Vacc

    更新日期:2010-06-08 00:00:00

  • Comparing survival curves based on medians.

    abstract:BACKGROUND:Although some nonparametric methods have been proposed in the literature to test for the equality of median survival times for censored data in medical research, in general they have inflated type I error rates, which make their use limited in practice, especially when the sample sizes are small. METHODS:In...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/s12874-016-0133-3

    authors: Chen Z,Zhang G

    更新日期:2016-03-16 00:00:00

  • Can electronic search engines optimize screening of search results in systematic reviews: an empirical study.

    abstract:BACKGROUND:Most electronic search efforts directed at identifying primary studies for inclusion in systematic reviews rely on the optimal Boolean search features of search interfaces such as DIALOG and Ovid. Our objective is to test the ability of an Ultraseek search engine to rank MEDLINE records of the included studi...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-6-7

    authors: Sampson M,Barrowman NJ,Moher D,Clifford TJ,Platt RW,Morrison A,Klassen TP,Zhang L

    更新日期:2006-02-24 00:00:00

  • Recruitment and retention in a multicentre randomised controlled trial in Bell's palsy: a case study.

    abstract:BACKGROUND:It is notoriously difficult to recruit patients to randomised controlled trials in primary care. This is particularly true when the disease process under investigation occurs relatively infrequently and must be investigated during a brief time window. Bell's palsy, an acute unilateral paralysis of the facial...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章,随机对照试验

    doi:10.1186/1471-2288-7-15

    authors: McKinstry B,Hammersley V,Daly F,Sullivan F

    更新日期:2007-03-28 00:00:00

  • Integrating and extending cohort studies: lessons from the eXtending Treatments, Education and Networks in Depression (xTEND) study.

    abstract:BACKGROUND:Epidemiologic studies often struggle to adequately represent populations and outcomes of interest. Differences in methodology, data analysis and research questions often mean that reviews and synthesis of the existing literature have significant limitations. The current paper details our experiences in combi...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-13-122

    authors: Allen J,Inder KJ,Lewin TJ,Attia JR,Kay-Lambkin FJ,Baker AL,Hazell T,Kelly BJ

    更新日期:2013-10-05 00:00:00

  • The fading of reported effectiveness. A meta-analysis of randomised controlled trials.

    abstract:BACKGROUND:The "real" effect size of a medical therapy is constant over time. In contrast, the effect size reported in randomised controlled trials (RCTs) may change over time because the sum of all kinds of bias influencing the reported effectiveness is not necessarily constant. As this would affect the validity of me...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章,meta分析

    doi:10.1186/1471-2288-6-25

    authors: Gehr BT,Weiss C,Porzsolt F

    更新日期:2006-05-11 00:00:00

  • Bias due to censoring of deaths when calculating extra length of stay for patients acquiring a hospital infection.

    abstract:BACKGROUND:In many studies the information of patients who are dying in the hospital is censored when examining the change in length of hospital stay (cLOS) due to hospital-acquired infections (HIs). While appropriate estimators of cLOS are available in literature, the existence of the bias due to censoring of deaths w...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/s12874-018-0500-3

    authors: Rahman S,von Cube M,Schumacher M,Wolkewitz M

    更新日期:2018-05-30 00:00:00

  • Pragmatic controlled clinical trials in primary care: the struggle between external and internal validity.

    abstract:BACKGROUND:Controlled clinical trials of health care interventions are either explanatory or pragmatic. Explanatory trials test whether an intervention is efficacious; that is, whether it can have a beneficial effect in an ideal situation. Pragmatic trials measure effectiveness; they measure the degree of beneficial ef...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-3-28

    authors: Godwin M,Ruhland L,Casson I,MacDonald S,Delva D,Birtwhistle R,Lam M,Seguin R

    更新日期:2003-12-22 00:00:00

  • Psychometric analysis of the brief symptom inventory 18 (BSI-18) in a representative German sample.

    abstract:BACKGROUND:The BSI-18 contains the three six-item scales somatization, depression, and anxiety as well as the Global Severity Index (GSI), including all 18 items. The BSI-18 is the latest and shortest of the multidimensional versions of the Symptom-Checklist 90-R, but its psychometric properties have not been sufficien...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/s12874-016-0283-3

    authors: Franke GH,Jaeger S,Glaesmer H,Barkmann C,Petrowski K,Braehler E

    更新日期:2017-01-26 00:00:00

  • A system for rating the stability and strength of medical evidence.

    abstract:BACKGROUND:Methods for describing one's confidence in the available evidence are useful for end-users of evidence reviews. Analysts inevitably make judgments about the quality, quantity consistency, robustness, and magnitude of effects observed in the studies identified. The subjectivity of these judgments in several a...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-6-52

    authors: Treadwell JR,Tregear SJ,Reston JT,Turkelson CM

    更新日期:2006-10-19 00:00:00

  • National weighting of data from the Behavioral Risk Factor Surveillance System (BRFSS).

    abstract:BACKGROUND:The Behavioral Risk Factor Surveillance System (BRFSS) is a network of health-related telephone surveys--conducted by all 50 states, the District of Columbia, and participating US territories-that receive technical assistance from CDC. Data users often aggregate BRFSS state samples for national estimates wit...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/s12874-016-0255-7

    authors: Iachan R,Pierannunzi C,Healey K,Greenlund KJ,Town M

    更新日期:2016-11-15 00:00:00

  • European Medicines Agency Policy 0070: an exploratory review of data utility in clinical study reports for academic research.

    abstract:BACKGROUND:Clinical study reports (CSRs) have been increasingly utilised within academic research in recent years. European Medicines Agency (EMA) Policy 0070 'Phase 1,' which came into effect in January 2015, requires the publication of regulatory documents such as CSRs from central applications in an anonymised forma...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章,评审

    doi:10.1186/s12874-019-0836-3

    authors: Ferran JM,Nevitt SJ

    更新日期:2019-11-05 00:00:00

  • Recruitment strategies and yields for the Pathobiology of Prediabetes in a Biracial Cohort: a prospective natural history study of incident dysglycemia.

    abstract:BACKGROUND:The Pathobiology of Prediabetes in A Biracial Cohort study is a prospective evaluation of the transition from normal to impaired glucose regulation among African American and Caucasian adults with parental type 2 diabetes. This report describes recruitment strategies and relative yields for the 376 enrolled ...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-13-64

    authors: Ebenibo S,Edeoga C,Ammons A,Egbuonu N,Dagogo-Jack S,Pathobiology of Prediabetes in a Biracial Cohort (POP-ABC) Research Group.

    更新日期:2013-05-10 00:00:00

  • The Platino project: methodology of a multicenter prevalence survey of chronic obstructive pulmonary disease in major Latin American cities.

    abstract:BACKGROUND:The prevalence of Chronic Obstructive Pulmonary Disease (COPD) in many developed countries appears to be increasing. There is some evidence from Latin America that COPD is a growing cause of death, but information on prevalence is scant. It is possible that, due to the high frequency of smoking in these coun...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-4-15

    authors: Menezes AM,Victora CG,Perez-Padilla R,PLATINO Team.

    更新日期:2004-06-17 00:00:00

  • Study protocol: the empirical investigation of methods to correct for measurement error in biobanks with dietary assessment.

    abstract:BACKGROUND:The Public Population Project in Genomics (P3G) is an organisation that aims to promote collaboration between researchers in the field of population-based genomics. The main objectives of P3G are to encourage collaboration between researchers and biobankers, optimize study design, promote the harmonization o...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-11-135

    authors: Bennett DA,Little J,Masson LF,Minelli C

    更新日期:2011-10-05 00:00:00

  • Is a large scale community programme as effective as a community rehabilitation programme delivered in the setting of a clinical trial?

    abstract:BACKGROUND:The rationale for commissioning community pulmonary rehabilitation programmes is based on evidence from randomised clinical trials. However, there are a number of reasons why similar programmes might be less effective outside the environment of a clinical trial. These include a less highly selected patient g...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-13-103

    authors: Goyder EC,Strong M,Green A,Holmes MW,Miles G,Reddington O,Lawson R,Lee A,Basran G

    更新日期:2013-08-13 00:00:00

  • The methods and baseline characteristics of a VA randomized controlled study evaluating supported employment provided in primary care patient aligned care teams.

    abstract:BACKGROUND:This article describes the design and baseline sample of a single-site trial comparing Individual Placement and Support (IPS) supported employment delivered within a Veterans Health Administration (VHA) primary care Patient Aligned Care Team (PACT) to treatment-as-usual vocational rehabilitation (TAU-VR) tha...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章,随机对照试验

    doi:10.1186/s12874-020-0919-1

    authors: Davis LL,Blansett CM,Mumba MN,MacVicar D,Toscano R,Pilkinton P,Gay W,Bartolucci A

    更新日期:2020-02-17 00:00:00

  • Using a social marketing framework to evaluate recruitment of a prospective study of genetic counseling and testing for the deaf community.

    abstract:BACKGROUND:Recruiting deaf and hard-of-hearing participants, particularly sign language-users, for genetics health service research is challenging due to communication barriers, mistrust toward genetics, and researchers' unfamiliarity with deaf people. Feelings of social exclusion and lack of social cohesion between re...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-13-145

    authors: Kobayashi Y,Boudreault P,Hill K,Sinsheimer JS,Palmer CG

    更新日期:2013-11-25 00:00:00

  • Understanding the predictive value of continuous markers for censored survival data using a likelihood ratio approach.

    abstract:BACKGROUND:The likelihood ratio function (LR), the ratio of conditional probabilities of obtaining a specific marker value among those with the event of interest over those without, provides an easily interpretable way to quantify the update of the risk prediction due to the knowledge of the marker value. The LR has be...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/s12874-019-0721-0

    authors: Smith AM,Christodouleas JP,Hwang WT

    更新日期:2019-05-22 00:00:00

  • Incongruence between test statistics and P values in medical papers.

    abstract:BACKGROUND:Given an observed test statistic and its degrees of freedom, one may compute the observed P value with most statistical packages. It is unknown to what extent test statistics and P values are congruent in published medical papers. METHODS:We checked the congruence of statistical results reported in all the ...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-4-13

    authors: García-Berthou E,Alcaraz C

    更新日期:2004-05-28 00:00:00

  • Interpreter proxy versus healthcare interpreter for administration of patient surveys following arthroplasty: a pilot study.

    abstract:BACKGROUND:Clinical quality registries and other systems that conduct routine post-discharge surveillance of patient outcomes following surgery may have difficulty surveying patients who have limited proficiency in the language of the healthcare provider. Interpreter proxies (family and carers) are often used due to li...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/s12874-019-0854-1

    authors: Xue D,Churches T,Armstrong E,Mittal R,Naylor JM,Harris IA

    更新日期:2019-11-14 00:00:00

  • Random allocation software for parallel group randomized trials.

    abstract:BACKGROUND:Typically, randomization software should allow users to exert control over the different aspects of randomization including block design, provision of unique identifiers and control over the format and type of program output. While some of these characteristics have been addressed by available software, none...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-4-26

    authors: Saghaei M

    更新日期:2004-11-09 00:00:00

  • Validation of the French version of the Vulnerable Elders Survey-13 (VES-13).

    abstract:BACKGROUND:Identifying and assessing degree and type of frailty among older persons is a major challenge when targeting high risk populations to identify preventive interventions. The Vulnerable Elders Survey-(VES-13) is a simple instrument to identify frailty defined as risk for death, functional decline or institutio...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/s12874-020-0910-x

    authors: Belmin J,Khellaf L,Pariel S,Jarzebowski W,Valembois L,Zeisel J,Lafuente-Lafuente C

    更新日期:2020-02-05 00:00:00

  • Variable selection in social-environmental data: sparse regression and tree ensemble machine learning approaches.

    abstract:BACKGROUND:Social-environmental data obtained from the US Census is an important resource for understanding health disparities, but rarely is the full dataset utilized for analysis. A barrier to incorporating the full data is a lack of solid recommendations for variable selection, with researchers often hand-selecting ...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/s12874-020-01183-9

    authors: Handorf E,Yin Y,Slifker M,Lynch S

    更新日期:2020-12-10 00:00:00

  • A transdisciplinary team approach to scoping reviews: the case of pediatric polypharmacy.

    abstract:BACKGROUND:Polypharmacy can be either beneficial or harmful to children. We conducted a scoping review to examine the concept of pediatric polypharmacy: its definition, prevalence, extent and gaps in research. In this manuscript, we report our transdisciplinary scoping review methodology. METHODS:After establishing a ...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/s12874-018-0560-4

    authors: Bakaki PM,Staley J,Liu R,Dawson N,Golchin N,Horace A,Johnson H,Waldron J,Winterstein A,Kleinman LC,Bolen SD

    更新日期:2018-10-04 00:00:00

  • Parental compliance--an emerging problem in Liverpool community child health surveys 1991-2006.

    abstract:BACKGROUND:Compliance is a critical issue for parental questionnaires in school based epidemiological surveys and high compliance is difficult to achieve. The objective of this study was to determine trends and factors associated with parental questionnaire compliance during respiratory health surveys of school childre...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-12-53

    authors: Koshy G,Brabin BJ

    更新日期:2012-04-20 00:00:00

  • The new COSMIN guidelines confront traditional concepts of responsiveness.

    abstract::The recently published "COSMIN" guidelines aim to rate properties of outcome instruments and state two issues with regard to responsiveness which is the instrument's ability to detect change over time. These issues are comparison of score changes with change of an external criterion using correlations and the judgemen...

    journal_title:BMC medical research methodology

    pub_type: 评论,信件

    doi:10.1186/1471-2288-11-152

    authors: Angst F

    更新日期:2011-11-18 00:00:00

  • Adaptive propensity score procedure improves matching in prospective observational trials.

    abstract:BACKGROUND:Randomized controlled trials are the gold-standard for clinical trials. However, randomization is not always feasible. In this article we propose a prospective and adaptive matched case-control trial design assuming that a control group already exists. METHODS:We propose and discuss an interim analysis step...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/s12874-019-0763-3

    authors: Weber D,Uhlmann L,Schönenberger S,Kieser M

    更新日期:2019-07-16 00:00:00

  • Error in statistical tests of error in statistical tests.

    abstract:BACKGROUND:A recent paper found that terminal digits of statistical values in Nature deviated significantly from an equiprobable distribution, indicating errors or inconsistencies in rounding. This finding, as well as the discovery that a large percentage of p values were inconsistent with reported test statistics, led...

    journal_title:BMC medical research methodology

    pub_type: 评论,杂志文章

    doi:10.1186/1471-2288-6-45

    authors: Jeng M

    更新日期:2006-09-13 00:00:00

  • Bivariate random-effects meta-analysis and the estimation of between-study correlation.

    abstract:BACKGROUND:When multiple endpoints are of interest in evidence synthesis, a multivariate meta-analysis can jointly synthesise those endpoints and utilise their correlation. A multivariate random-effects meta-analysis must incorporate and estimate the between-study correlation (rhoB). METHODS:In this paper we assess ma...

    journal_title:BMC medical research methodology

    pub_type: 杂志文章

    doi:10.1186/1471-2288-7-3

    authors: Riley RD,Abrams KR,Sutton AJ,Lambert PC,Thompson JR

    更新日期:2007-01-12 00:00:00