ArticleJAMA surgery2015
Time required for institutional review board review at one Veterans Affairs medical center.
Article in JAMA surgery, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled 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.
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
14 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Evaluating IACUCs: Previous Research and Future Directions.Journal of the American Association for Laboratory Animal Science : JAALAS · 2020Pooled it
- From Insights to Action: Enhancing Clinical Research at The Ottawa Hospital through a Mixed-Methods Improvement Project.Healthcare management forum · 2026Article
- Understanding Ethical Concerns Involving Vulnerable Human Participant Populations in Medical Research: Mixed-Method Analysis of Liberian Ebola Survivors' Experiences in PREVAIL I-VII.Healthcare (Basel, Switzerland) · 2024Article
- New Anticancer Drugs: Reliably Assessing "Value" While Addressing High Prices.Current oncology (Toronto, Ont.) · 2024Article
- The Benefit of an Umbrella Protocol: Reducing Challenges in Orthopedic Oncology Research.Journal of clinical medicine · 2024Article
- Article
- DataSifter II: Partially synthetic data sharing of sensitive information containing time-varying correlated observations.Journal of algorithms & computational technology · 2022Article
- Health informatics and EHR to support clinical research in the COVID-19 pandemic: an overview.Briefings in bioinformatics · 2021Review
- A Rare Opportunity: Examining the Experience of a New Institutional Review Board.Journal of empirical research on human research ethics : JERHRE · 2019Article
- Regulatory Support Improves Subsequent IRB Approval Rates in Studies Initially Deemed Not Ready for Review: A CTSA Institution's Experience.Journal of empirical research on human research ethics : JERHRE · 2018Article
- Time required to initiate outbreak and pandemic observational research.Journal of critical care · 2017Article
- Effects of Regulatory Support Services on Institutional Review Board Turnaround Times.Journal of empirical research on human research ethics : JERHRE · 2017Article
- Time required to review research protocols at 10 Veterans Affairs Institutional Review Boards.The Journal of surgical research · 2016Article
- A personalized Institutional Review Board Liaison Service: Evaluation over its initial 30 months.International journal of academic medicineArticle
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
importanceDespite growing concern that institutional review boards (IRBs) impose burdensome delays on research, little is known about the time required for IRB review across different types of research.
objectiveTo measure the overall and incremental process times for IRB review as a process of quality improvement. DESIGN, SETTING, AND
participantsAfter developing a detailed process flowchart of the IRB review process, 2 analysts abstracted temporal data from the records pertaining to all 103 protocols newly submitted to the IRB at a large urban Veterans Affairs medical center from June 1, 2009, through May 31, 2011. Disagreements were reviewed with the principal investigator to reach consensus. We then compared the review times across review types using analysis of variance and post hoc Scheffé tests after achieving normally distributed data through logarithmic transformation. MAIN OUTCOMES AND MEASURES: Calendar days from initial submission to final approval of research protocols.
resultsInitial IRB review took 2 to 4 months, with expedited and exempt reviews requiring less time (median [range], 85 [23-631] and 82 [16-437] days, respectively) than full board reviews (median [range], 131 [64-296] days; P = .008). The median time required for credentialing of investigators was 1 day (range, 0-74 days), and review by the research and development committee took a median of 15 days (range, 0-184 days). There were no significant differences in credentialing or research and development times across review types (exempt, expedited, or full board). Of the extreme delays in IRB review, 80.0% were due to investigators' slow responses to requested changes. There were no systematic delays attributable to the information security officer, privacy officer, or IRB chair. CONCLUSIONS AND RELEVANCE: Measuring and analyzing review times is a critical first step in establishing a culture and process of continuous quality improvement among IRBs that govern research programs. The review times observed at this IRB are substantially longer than the 60-day target recommended by expert panels. The method described here could be applied to other IRBs to begin identifying and improving inefficiencies.
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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.