Evidence map›Paper›PMID 39948475›Full record

ArticleBMC medical research methodology2025

Improving research transparency with individualized report cards: A feasibility study in clinical trials at a large university medical center.

Delwen L Franzen, Maia Salholz-Hillel, Stephanie Müller-Ohlraun, Daniel Strech

Abstract read
In one paragraph

Article in BMC medical research methodology, 2025. 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
–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

3 citing papers in PubMed.

  1. Observational
  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

4 authors.

Delwen L Franzen *Berlin Institute of Health at Charité - Universitätsmedizin Berlin, QUEST Center for Responsible Research, Charitéplatz 1, 10117, Berlin, Germany. delwen.franzen@bih-charite.de.ORCID 0000-0001-9974-9115
Maia Salholz-Hillel *Berlin Institute of Health at Charité - Universitätsmedizin Berlin, QUEST Center for Responsible Research, Charitéplatz 1, 10117, Berlin, Germany. maia.salholz-hillel@bih-charite.de.ORCID 0000-0003-1934-9504
Stephanie Müller-OhlraunBerlin Institute of Health at Charité - Universitätsmedizin Berlin, QUEST Center for Responsible Research, Charitéplatz 1, 10117, Berlin, Germany.ORCID 0000-0002-8495-6135
Daniel StrechBerlin Institute of Health at Charité - Universitätsmedizin Berlin, QUEST Center for Responsible Research, Charitéplatz 1, 10117, Berlin, Germany.ORCID 0000-0002-9153-079X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundResearch transparency is crucial for ensuring the relevance, integrity, and reliability of scientific findings. However, previous work indicates room for improvement across transparency practices. The primary objective of this study was to develop an extensible tool to provide individualized feedback and guidance for improved transparency across phases of a study. Our secondary objective was to assess the feasibility of implementing this tool to improve transparency in clinical trials.

methodsWe developed study-level "report cards" that combine tailored feedback and guidance to investigators across several transparency practices, including prospective registration, availability of summary results, and open access publication. The report cards were generated through an automated pipeline for scalability. We also developed an infosheet to summarize relevant laws, guidelines, and resources relating to transparency. To assess the feasibility of using these tools to improve transparency, we conducted a single-arm intervention study at Berlin's university medical center, the Charité - Universitätsmedizin Berlin. Investigators (n = 92) of 155 clinical trials were sent individualized report cards and the infosheet, and surveyed to assess their perceived usefulness. We also evaluated included trials for improvements in transparency following the intervention.

resultsSurvey responses indicated general appreciation for the report cards and infosheet, with a majority of participants finding them helpful to build awareness of the transparency of their trial and transparency requirements. However, improvement on transparency practices was minimal and largely limited to linking publications in registries. Investigators also commented on various challenges associated with implementing transparency, including a lack of clarity around best practices and institutional hurdles.

conclusionsThis study demonstrates the potential of developing and using tools, such as report cards, to provide individualized feedback at scale to investigators on the transparency of their study. While these tools were positively received by investigators, the limited improvement in transparency practices suggests that awareness alone is likely not sufficient to drive improvement. Future research and implementation efforts may adapt the tools to further practices or research areas, and explore integrated approaches that combine the report cards with incentives and institutional support to effectively strengthen transparency in research.

Indexed as

Academic Medical CentersBiomedical ResearchClinical Trials as TopicResearch DesignFeasibility StudiesHumansResearch PersonnelSurveys and QuestionnairesClinical trialsFeedbackResearch transparencyTools

Identifiers

PMID39948475
PMCPMC11823227

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.