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Quality of pilot trial abstracts in heart failure is suboptimal: a systematic survey
© The Author(s). 2018
- Received: 18 January 2018
- Accepted: 23 May 2018
- Published: 31 May 2018
Pilot trials are miniature researches carried out with the sole aim of acting as the precursor for larger more definitive studies. Abstracts are used to summarize and introduce the findings to the reading audience. There is substantive empirical evidence showing that abstracts, despite their important roles, are not informative enough, lacking the necessary details. This systematic survey was designed to assess the quality of reporting of heart failure pilot trial abstracts. The quality of reporting was defined as the completeness of reporting based on adherence to the CONSORT extension for reporting of pilot trial abstracts. We also identified factors associated with reporting quality.
We searched MEDLINE (PubMed), Cochrane Controlled Trials Register, Scopus, and African-wide information databases for abstracts from heart failure pilot trials in humans published from 1 January 1990 to 30 November 2016. These were assessed to determine the extent of adherence to CONSORT extension checklist for reporting of abstracts of pilot trials. We screened identified studies for inclusion based on title and abstract. Data were independently extracted by two reviewers using the checklist. We used regression analysis to assess the association between completeness of reporting (measured as the number of items in the CONSORT extension checklist for reporting of abstracts in pilot trials contained in each abstract) and factors influencing the quality of the reports.
Two hundred and twenty-eight (228) articles were retrieved, of which 92 met the inclusion criteria. The mean CONSORT extension score was 8.3/16 (standard deviation 1.7); the least reported items were the source of funding (1% [1/92]), trial registration (13% [12/92]), randomization sequence (13% [12/92]), number randomized to each arm (16% [15/92]), and number analyzed in each arm (16% [15/92]). Multivariable regression analysis showed that pharmacological intervention pilot trials [incidence rate ratio (IRR) = 0.88; 95% confidence interval (CI), 0.81–0.97] were significantly associated with better reporting. Other factors such as structured abstract (IRR = 1.10; 95% CI, 0.99–1.23) and CONSORT endorsement (IRR = 1.10; 95% CI, 0.99–1.23) only showed minimal relationship with better reporting quality.
The quality of reporting of abstracts of heart failure pilot trials was suboptimal. Pharmacological intervention was significantly associated with better reporting. These findings are consistent with previous research on reporting of trials.
Numerous challenges confront readers while accessing the literature; these include but are not limited to the enormous volume of published work, the high cost of obtaining articles especially in resource-limited settings , and language constraints when articles are not written in users’ language . The outcome of this has been an over-reliance on abstracts for articles as a one-stop point for most researchers. Abstracts of journal articles or scientific papers often provide readers with an overview of the content of the full article. As a result, researchers tend to rely on abstracts as a concise source of information  and in making decisions on which publications to read in detail . Furthermore, researchers rely largely on the abstract when deciding whether to include an article in a systematic review . All these factors make the abstract a key section of the scientific publication. It is, therefore, important that abstracts of articles are consistent with what is reported in the text and capture essential information.
Randomized control trials (RCT) constitute a significant portion of clinical studies and most times are the core component for systematic reviews. However, the quality of reporting of RCTs have over the years attracted many questions, mostly related to consistency and completeness of reports . The Consolidated Standard for Reporting of Trials (CONSORT) checklist was conceptualized in 1996 to address these issues. Its publication and instant acceptance led to revisions in 2007 and 2010 [7, 8]. Many journals have adopted the CONSORT checklist, and it has been shown to improve the quality of reporting RCTs [9–11].
The overwhelming acceptance of CONSORT checklist has led to the development of extensions to incorporate other types of RCTs. Due to the need to widen the scope of the checklist, in 2016, the CONSORT extension checklist for abstracts of pilot trials was developed to aid adequate reporting of pilot trials , an important but often neglected arm of medical research .
We conducted this systematic survey to evaluate the quality of reporting of abstracts of pilot RCTs in heart failure published 1990–2016. Heart failure, defined as a clinical condition in which the heart does not pump blood sufficiently or does so at a higher pressure to maintain the body’s need [14, 15], has been a prominent cause of cardiovascular disease burden in Africa in the last two decades [16, 17]. It has also attracted many clinical trials in the last two decades (1990–2016), most of which were preceded by pilot trials . The quality reporting is defined as complete reporting of the 16 items in the CONSORT extension checklist.
The aims of this survey are to (1) evaluate the quality of reporting of abstracts of pilot RCTs in the past 26 years (1990–2016), using the CONSORT extension for reporting of abstracts of pilot trials; (2) identify aspects of the checklist that are consistently reported; (3) identify factors associated with better reporting of abstracts; and (4) determine the quality (completeness) of abstracts of pilot trials.
Randomized controlled pilot trials in heart failure published from 1 January 1990 to 30 November 2016 were searched for in line with the systematic survey method as previously described . Abstracts were selected if they were described as random, randomly allocated, and randomized. We searched the MEDLINE (PubMed), Cochrane Controlled Trials Register, Scopus, and African-wide information databases (search strategy in the Additional file 1). We limited our search to pilot trial reports written in English language only. Two reviewers independently screened the identified papers and those finally selected to assess the quality of reporting of abstracts using the 16 items of CONSORT extension for reporting of abstract of pilot trials. We assigned a score of one to an item on the CONSORT checklist if the item was reported in the abstract. The overall quality of abstract was calculated as the proportion of “yes” responses. We classified abstracts that reported all the 16 items in the CONSORT checklist as adequate quality reporting.
We hypothesized that pilot trials published in high impact journals , published in CONSORT-endorsing journals [19, 20], those on pharmacological interventions , studies with large sample sizes , and industry-funded studies  would have better reporting quality.
The protocol for this systematic survey  was registered with PROSPERO (CRD42016049911) and written according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis Extension for Protocols (PRISMA-P) .
The analysis was with IBM statistical package for social sciences (IBM SPSS) version 24 (IBM Corp., Armonk, NY) and STATA 9.0 (College Station, TX). We calculated the percentage of trials that scored yes on each of the 16 items and the associated 95% confidence interval (CI).
We reported categorical variables as count and percentages; continuous variables are summarized as mean (standard deviation (SD)) or median (interquartile range (IQR)). Incidence risk ratio (IRR) was calculated to identify factors associated with better reporting. Negative binomial regression was conducted to determine factors associated with better reporting quality.
Characteristics of included papers: n = 92
Count (%)/median (Q1; Q3)
Year of publication
Intervention type (n = 90)
Both pharmacological and non-pharmacological
Number of sites
Study duration in months (n = 68)
3.0 (2.6; 6.1)
Sample size (n = 88)
41 (24; 88)
Quality of reporting of abstracts of pilot trials
Publication adherence to CONSORT checklist for abstract of pilot trials n = 92
Percent (95% CI)
Title identifies the study is a randomized controlled pilot trial
71 (60; 79)
Description of pilot trial design (e.g., parallel or cluster)
33 (23; 44)
Eligibility criteria for each participant
88 (78; 94)
Setting where pilot was conducted
32 (22; 47)
Interventions intended for each group
99 (91; 99)
Specific objectives of the pilot trial
94 (89; 99)
Pre-specified assessment or measurement to address the pilot trial objectives
97 (90; 98)
Randomization sequence generation
Describe how participants were allocated to the interventions
13 (8; 19)
Whether or not participants, caregivers, and those assessing the outcomes were blinded to group assignment
22 (15; 31)
Number of participants screened
16 (9; 26)
Number randomized to each group for the pilot objectives
45 (36; 53)
Trial status (for conference abstracts)
2 (5; 8)
Number of participants analyzed in each group of pilot objectives
16 (11; 24)
Important adverse events or side effects
30 (23; 39)
General interpretation of results of pilot trial
Any implication for future trial
22 (15; 30)
Registration number of trial
13 (7; 21)
Source of funding
1 (0.16; 6.9)
The least reported item was funding source 1% (95% CI 0.16; 6.9); however, 21 of 92 (22.8%) studies reported funding source in the main manuscript but not in the abstract. Inadequately reported items include the randomization method used 13% (95% CI 8; 19), trial registration information 13% (95% CI 7; 21), and the number of participants screened in each arm 16% (95% CI 9; 26). Recruitment status, an item in the CONSORT checklist that addresses conference presentation, was low with 2% (95% CI 5; 8) among the 12 conference abstracts.
Univariate and multivariable analysis of factors associated with reported items
IRR (95% CI)
IRR (95% CI)
Year of publication
0.99 (0.91; 1.08)
1.07 (0.91; 1.13)
0.93 (0.86; 1.01);
0.88 (0.81; 0.97)
1.11 (0.99; 1.24)
1.10 (0.99; 1.23)
1.07 (0.98; 1.16)
1.10 (0.99; 1.23)
Number of sites
1.08 (0.97; 1.22)
1.02 (0.92; 1.15)
1.03 (1.01; 1.06)
1.01 (0.96; 1.07)
The CONSORT extension for reporting of abstracts of pilot trials was introduced in 2016 to standardize the reporting of abstracts of such studies. We undertook this survey to gauge the current practice using heart failure pilot trials as a sample to track reporting quality improvement expected with introduction and adherence to the extension. We found inadequate reporting quality in keeping with previous articles evaluating adherence to CONSORT checklist on abstracts [8, 24, 25].
The least reported item was the funding source, similar to findings in a previous study . The full declaration of funding source in a publication can give the reader the opportunity to make their own assessment regarding potential conflict of interest. However, we noticed that 22/96 of the articles had information on funding in other places rather than the abstract, and this may not be unrelated to word count stipulation by individual journals. Often, this poses a challenge to authors on what to include in abstracts, and there may be the need for CONSORT extension checklist developers to consider this limitation.
The randomization sequence was also poorly reported. It is an item that can provide acceptable comparability between groups if properly reported. Some previous studies have commented on this methodological flaw [10, 27–29], explaining that this could be because of attachment of more relevance to clinical than the methodological aspect of RCTs. There has been corroborating evidence in other studies supporting a correlation between deficient reporting and poor trial methodology [30–32].
Many of the articles were also silent on the blinding, and when used, some failed to state the group blinded in the studies. Not being explicit about blinding erodes the integrity and internal validity of the reports, and it is a potential source of bias among the readers [33, 34]. Reporting on harm was low at 28%; this is an essential item as it informs the design and applicability of intended larger trials. Previously, this safety reporting has often been inadequate or neglected . And, in literature, there is highly variable adherence to reporting of harm [36, 37].
Methodological aspects reported include intervention type, specific objective, and outcomes to be assessed. Many of the articles identified them as pilot trials; this was despite the constraint of word limit by journals, a reason often adduced as responsible for not including this [10, 26, 29]. Also, pilot trials with pharmacological intervention, those with structured abstracts, and those published in the journal that endorses CONSORT were more likely to report on the items on the checklist. The last point brings to fore why it is important for journals to have stipulated reporting format to ensure that the quality of abstracts’ report is improved.
Our study is limited in scope by using only articles published in the English language. We also used a recently produced checklist to evaluate publications done by authors who at the time of writing of the articles probably had no reporting checklist to follow.
In conclusion, the reporting quality of abstracts of heart failure trial measured by the number of items reported was suboptimal; the need to guard against this was the reason that informed the introduction of CONSORT extension checklist. The desire is that increasingly journals will demand adherence to the checklist by authors. Ultimately, we hope that there will be a marked improvement in the quality of report of abstracts in the coming years.
Godsent Chichebem Isiguzo is on a PhD scholarship of Postgraduate academic mobility for African Physician-Scientist (PAMAPS), funded under the intra-ACP Academic mobility scheme of European Union.
Availability of data and materials
The data and materials are available on request from the authors.
GI, LT, BM, MZ, and MC made a substantial contribution to the conceptualization and design, acquisition of data, analysis, and interpretation. GC, LT, and BM have been involved in drafting the manuscript and revising the content for important intellectual content. BM, LT, GC, MC, and MZ gave the final approval of the version to be published. LT, BM, GC, MZ, and MC agreed to be accountable for all aspects of the work in ensuring accuracy and intellectual content.
Ethics approval and consent to participate
The study did not involve any human subjects, so ethics approval or consent was not required.
The authors declare that they have no competing interests.
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