Javascript must be enabled to continue!
P-746 Recruitment in randomised controlled trials: a conundrum
View through CrossRef
Abstract
Study question
What factors are associated with recruitment failure within the pre-planned study period?
Summary answer
Trials with a no-treatment arm, over four inclusion criteria, without a previous pilot and with low funding, are more likely to experience recruitment failure.
What is known already
Randomised controlled trials are considered to be the best strategy in evaluating the effectiveness of medical interventions, but they are often hampered by failure to recruit enough patients with the pre-planned study period. This represents a form of research waste. Little is known on variables related to recruitment failure within the pre-planned study period.
Study design, size, duration
This study was designed as a nationwide cohort study and included 71 randomized controlled trials supported by the Dutch Consortium for Women’s Health Research. We included trials initiated between March 1st 2003 and March 1st 2022. We extracted study data and information on predefined barriers and facilitators.
Participants/materials, setting, methods
Primary outcome was recruitment target not achieved within 6 months after the pre-planned recruitment period. Secondary outcomes included recruitment target not achieved within an extension of at least 12 months and premature termination of the trial. We used logistic regression to evaluate the association between potential indicators of recruitment failure and expressed these as odds ratios (OR) with corresponding 95% confidence intervals (CI).
Main results and the role of chance
Of the 71 trials included in our cohort, recruitment was not achieved within the pre-planned study period with a maximal extension period of 6 months or 12 months in 38 (54%) and 33 trials (46%), respectively. Indicators associated with higher chances on recruitment failure were a no treatment arm (OR 8.53 (95% CI 1.01 to 72.36)), a compensation fee of less than 200 euros per included patient (OR 3.16 (95% CI 1.18 to 8.45)) and a funding of less than 350.000 euros (OR 4.30 (95% CI 1.56 to 11.64)). Indicators associated with lower chances on recruitment failure were less than 4 inclusion criteria (OR 0.31 (95% CI 0.10 to 0.97)) and a preceding pilot study (OR 0.53 (95% CI 0.15 to 1.85)).
Limitations, reasons for caution
If we could have accessed an even larger cohort of studies we might have been able to identify more potential indicators for recruitment failure.
Wider implications of the findings
Investigators and grantproviders should consider our findings before the start of their studies, to optimize recruitmentcircumstances. If a trial is destined to have a suspected long recruitment, it seems wise to consider the relevance and urgency of the research question, and then accept a longer recruitment period with its consequences.
Trial registration number
not applicable
Oxford University Press (OUP)
Title: P-746 Recruitment in randomised controlled trials: a conundrum
Description:
Abstract
Study question
What factors are associated with recruitment failure within the pre-planned study period?
Summary answer
Trials with a no-treatment arm, over four inclusion criteria, without a previous pilot and with low funding, are more likely to experience recruitment failure.
What is known already
Randomised controlled trials are considered to be the best strategy in evaluating the effectiveness of medical interventions, but they are often hampered by failure to recruit enough patients with the pre-planned study period.
This represents a form of research waste.
Little is known on variables related to recruitment failure within the pre-planned study period.
Study design, size, duration
This study was designed as a nationwide cohort study and included 71 randomized controlled trials supported by the Dutch Consortium for Women’s Health Research.
We included trials initiated between March 1st 2003 and March 1st 2022.
We extracted study data and information on predefined barriers and facilitators.
Participants/materials, setting, methods
Primary outcome was recruitment target not achieved within 6 months after the pre-planned recruitment period.
Secondary outcomes included recruitment target not achieved within an extension of at least 12 months and premature termination of the trial.
We used logistic regression to evaluate the association between potential indicators of recruitment failure and expressed these as odds ratios (OR) with corresponding 95% confidence intervals (CI).
Main results and the role of chance
Of the 71 trials included in our cohort, recruitment was not achieved within the pre-planned study period with a maximal extension period of 6 months or 12 months in 38 (54%) and 33 trials (46%), respectively.
Indicators associated with higher chances on recruitment failure were a no treatment arm (OR 8.
53 (95% CI 1.
01 to 72.
36)), a compensation fee of less than 200 euros per included patient (OR 3.
16 (95% CI 1.
18 to 8.
45)) and a funding of less than 350.
000 euros (OR 4.
30 (95% CI 1.
56 to 11.
64)).
Indicators associated with lower chances on recruitment failure were less than 4 inclusion criteria (OR 0.
31 (95% CI 0.
10 to 0.
97)) and a preceding pilot study (OR 0.
53 (95% CI 0.
15 to 1.
85)).
Limitations, reasons for caution
If we could have accessed an even larger cohort of studies we might have been able to identify more potential indicators for recruitment failure.
Wider implications of the findings
Investigators and grantproviders should consider our findings before the start of their studies, to optimize recruitmentcircumstances.
If a trial is destined to have a suspected long recruitment, it seems wise to consider the relevance and urgency of the research question, and then accept a longer recruitment period with its consequences.
Trial registration number
not applicable.
Related Results
Current therapeutic strategies for erectile function recovery after radical prostatectomy – literature review and meta-analysis
Current therapeutic strategies for erectile function recovery after radical prostatectomy – literature review and meta-analysis
Radical prostatectomy is the most commonly performed treatment option for localised prostate cancer. In the last decades the surgical technique has been improved and modified in or...
SISTEM REKRUITMEN DAN KADERISASI PARTAI KEADILAN SEJAHTERA DI JAWA BARAT
SISTEM REKRUITMEN DAN KADERISASI PARTAI KEADILAN SEJAHTERA DI JAWA BARAT
This research entitled �the system of Recruitmen and the prosperous justice party cadre recruitment in West Java�. The real problem in this research not yet optimal recruitment and...
Limpet disturbance effects on barnacle recruitment are related to recruitment intensity but not recruit size
Limpet disturbance effects on barnacle recruitment are related to recruitment intensity but not recruit size
Intertidal limpets are important grazers along rocky coastlines worldwide that not only control algae but also influence invertebrates such as common barnacles. For instance, grazi...
Benchmarking observational studies against randomised trials
Benchmarking observational studies against randomised trials
<p dir="ltr">Randomised trials are regarded as the gold standard in evaluating the effectiveness and safety of medical interventions, but they are not always feasible due to ...
Benchmarking observational studies against randomised trials
Benchmarking observational studies against randomised trials
<p dir="ltr">Randomised trials are regarded as the gold standard in evaluating the effectiveness and safety of medical interventions, but they are not always feasible due to ...
Clinical trial recruitment – a complex intervention?
Clinical trial recruitment – a complex intervention?
Aims and objectivesTo discuss the evidence of poor recruitment rates in randomised clinical trials and relate this to existing recruitment methodology before a novel approach to re...
Defining the Features of Registry Based Randomised Controlled Trials (rRCT): A Systematic Review
Defining the Features of Registry Based Randomised Controlled Trials (rRCT): A Systematic Review
Abstract
Background: Registry Based Randomised Controlled Trials have been described as pragmatic studies utilising patient data embedded in large scale registries, to faci...
Evaluating how clear the questions being investigated in randomised trials are: systematic review of estimands
Evaluating how clear the questions being investigated in randomised trials are: systematic review of estimands
AbstractObjectivesTo evaluate how often the precise research question being addressed about an intervention (the estimand) is stated or can be determined from reported methods, and...

