ArticleApplied clinical informatics2018
Exploring Data Quality Management within Clinical Trials.
Article in Applied clinical informatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.
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.
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.
Who cites it
20 citing papers in PubMed, 44 citations in OpenAlex.
- Utilization of stakeholder engagement to inform the identification of leading indicators for clinical research enrollment performance in a large integrated health care system: The VA clinical research enrollment summit.Contemporary clinical trials communications · 2026Article
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- Data capture, collection, management, and storage systems for clinical research: A scoping review protocol.PloS one · 2026Article
- Study protocol of sustaining home palliative care for patients with Heart Failure (HF) and their family caregivers in rural Appalachia: a mixed methods randomized clinical trial.BMC palliative care · 2025Article
- Phase 1 Clinical Trials: Challenges and Opportunities in Latin America.Journal of immunotherapy and precision oncology · 2024Article
- Source Data Verification (SDV) quality in clinical research: A scoping review.Journal of clinical and translational science · 2024Article
- Data Quality in Health Research: Integrative Literature Review.Journal of medical Internet research · 2023Review
- Data Management 101 for drug developers: A peek behind the curtain.Clinical and translational science · 2023Review
- Performance of four centralized statistical monitoring methods for early detection of an atypical center in a multicenter study.Contemporary clinical trials communications · 2023Article
- Approaches for enhancing the informativeness and quality of clinical trials: Innovations and principles for implementing multicenter trials from the Trial Innovation Network.Journal of clinical and translational science · 2023Article
- Performance and usability evaluation of a mobile health data capture application in clinical cancer trials follow-up.Technical innovations & patient support in radiation oncology · 2022Article
- Clinical researchers' lived experiences with data quality monitoring in clinical trials: a qualitative study.BMC medical research methodology · 2021Article
- Implementing an automated monitoring process in a digital, longitudinal observational cohort study.Arthritis research & therapy · 2021Observational
- New approaches to symptomatic treatments for Alzheimer's disease.Molecular neurodegeneration · 2021Review
- A Rule-Based Data Quality Assessment System for Electronic Health Record Data.Applied clinical informatics · 2020Article
- Quality Management Model for Phase I Clinical Drug Trials: A Structural Equation Model.Current medical science · 2020Article
- High throughput image labeling on chest computed tomography by deep learning.Journal of medical imaging (Bellingham, Wash.) · 2020Article
- Impact of a targeted monitoring on data-quality and data-management workload of randomized controlled trials: A prospective comparative study.British journal of clinical pharmacology · 2019Article
- Adapting data management education to support clinical research projects in an academic medical center.Journal of the Medical Library Association : JMLA · 2019Article
- Defining and Developing a Generic Framework for Monitoring Data Quality in Clinical Research.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2018Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundClinical trials are an important research method for improving medical knowledge and patient care. Multiple international and national guidelines stipulate the need for data quality and assurance. Many strategies and interventions are developed to reduce error in trials, including standard operating procedures, personnel training, data monitoring, and design of case report forms. However, guidelines are nonspecific in the nature and extent of necessary methods.
objectiveThis article gathers information about current data quality tools and procedures used within Australian clinical trial sites, with the aim to develop standard data quality monitoring procedures to ensure data integrity.
methodsRelevant information about data quality management methods and procedures, error levels, data monitoring, staff training, and development were collected. Staff members from 142 clinical trials listed on the National Health and Medical Research Council (NHMRC) clinical trials Web site were invited to complete a short self-reported semiquantitative anonymous online survey.
resultsTwenty (14%) clinical trials completed the survey. Results from the survey indicate that procedures to ensure data quality varies among clinical trial sites. Centralized monitoring (65%) was the most common procedure to ensure high-quality data. Ten (50%) trials reported having a data management plan in place and two sites utilized an error acceptance level to minimize discrepancy, set at <5% and 5 to 10%, respectively. The quantity of data variables checked (10-100%), the frequency of visits (once-a-month to annually), and types of variables (100%, critical data or critical and noncritical data audits) for data monitoring varied among respondents. The average time spent on staff training per person was 11.58 hours over a 12-month period and the type of training was diverse.
conclusionClinical trial sites are implementing ad hoc methods pragmatically to ensure data quality. Findings highlight the necessity for further research into "standard practice" focusing on developing and implementing publically available data quality monitoring procedures.
Indexed as
Identifiers
What OpenQuestion holds
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.