- Study protocol
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Enhancing Recruitment Using Teleconference and Commitment Contract (ERUTECC): study protocol for a randomised, stepped-wedge cluster trial within the EFFECTS trial
Trials volume 19, Article number: 14 (2018)
Many randomised controlled trials (RCTs) fail to meet their recruitment goals in time. Trialists are advised to include study recruitment strategies within their trials.
EFFECTS is a Swedish, academic-led RCT of fluoxetine for stroke recovery. The trial’s primary objective is to investigate whether 20 mg fluoxetine daily compared with placebo for 6 months after an acute stroke improves the patient’s functional outcome. The first patient was included on 20 October 2014 and, as of 31 August 2017, EFFECTS has included 810 of planned 1500 individuals. EFFECTS currently has 32 active centres.
The primary objective of the ERUTECC (Enhancing Recruitment Using Teleconference and Commitment Contract) study is to investigate whether a structured teleconference re-visit with the study personnel at the centres, accompanied by a commitment contract, can enhance recruitment by 20% at 60 days post intervention, compared with 60 days pre-intervention, in an ongoing RCT.
ERUTECC is a randomised, stepped-wedge cluster trial embedded in EFFECTS. The plan is to start ERUTECC with a running-in period of September 2017. The first intervention is due in October 2017, and the study will continue for 12 months. We are planning to intervene at all active centres in EFFECTS, except the five top recruiting centres (n = 27). The rationale for not intervening at the top recruiting centres is that we believe they have reached their full potential and the intervention would be too weak for them. The hypothesis of this study is that a structured teleconference re-visit with the study personnel at the centres, accompanied by a commitment contract, can enhance recruitment by 20% 60 days post intervention, compared to 60 days pre-intervention, in an ongoing RCT.
EFFECTS is a large, pragmatic RCT of stroke in Sweden. Results from the embedded ERUTECC study could probably be generalised to high-income Western countries, and is relevant to trial management and could improve trial management in the future. It might also be useful in clinical settings outside the field of stroke.
The ERUTECC study was registered in the Northern Ireland Hub for Trials Methodology Research Studies Within a Trial repository (SWAT58) on 30 April 2017.
ClinicalTrials.gov, ID: NCT02683213. Retrospectively registered on 2 February 2016.
Many randomised controlled trials (RCTs) fail to meet their recruitment goals in time [1, 2]. A study of 114 multicentre trials in the UK showed that 45% failed to reach 80% of their recruitment goal. Less than one third of the trials recruited their original target number of participants within the time originally specified, and around one third had to be extended in terms of time and resources , and it has been identified as the highest priority to find methods to enhance recruitment to the RCT . There are a few trials that have sought to evaluate different strategies for recruiting patients. However, these studies are small, and some are hypothetical, making the interpretation unclear . Qualitative interventions within trials to improve recruitment have been developed in the UK , and in addition, online resources [7, 8] are available. In spite of that, we need to know more about the barrier and success factors for trials in recruiting patients and especially in RCTs. Given these facts, trialists are advised to include study recruitment strategies within their trials .
One alternative is to embed trials of recruitment interventions within host trials. An embedded recruitment trial is defined as :
‘…a RCT in which an intervention (or several interventions) to enhance recruitment outcomes are tested in the context of another RCT (or several RCTs) known as the host RCT(s)’.
The EFFECTS (Efficacy oF Fluoxetine – a randomisEd Controlled Trial in Stroke, Clinical Trials number NCT02683213) study seeks to investigate whether 20 mg fluoxetine daily compared with placebo for 6 months after acute stroke improves patients’ functional outcome . The EFFECTS study is a multicentre trial aiming to recruit 1500 patients in Sweden. The study collaborates with two other investigator-led studies, FOCUS (UK) and AFFINITY (Australia/New Zealand/Vietnam). Each trial is funded independently and intends to report its own results .
The first patient in EFFECTS was included on 20 October 2014. Our primary recruitment goal was that each centre should randomise at least two patients per month. In reality, there are huge differences between centres regarding recruitment. Looking back between June 2016 and May 2017, for instance, only three centres have achieved the recruitment goal: Danderyd Hospital, Karolinska University Hospital Solna and Sundsvall Hospital, while another three (Mora General Hospital, Alingsås General Hospital and Skaraborg Hospital Skövde) came close. In fact, these six centres have so far included half of the individuals. This pattern – that a few centres have included the majority of individuals – has been consistent since the start, irrespective of different strategies. The recruitment rate per month and centre is updated in real time and is available in the public domain .
Rationales for the study
Currently, the EFFECTS trial includes 30 patients per month , and recruitment projections would take the trial beyond its current funding. Thus, a new strategy is needed.
After talking to the principal investigators (PIs) at the centres, and to trialists in the UK with similar studies, we are confident that five of the top recruiters (Danderyd Hospital, Karolinska University Hospital Solna, Sundsvall Hospital, Mora General Hospital and Skaraborg Hospital Skövde) have reached their full potential, and little would be gained from the planned intervention.
We have asked the centres via a survey, and have also discussed this in person at investigator meetings, what they consider to be the most important barrier to recruitment for trials. They have said that the most important barrier is the lack of time for the physician responsible to identify the right patients and to carry out the study-specific procedures at baseline. The second most important factor is the lack of time for all other study personnel. They have a high clinical workload at their clinic and do not have any time specifically dedicated to working with clinical trials. It is the head of department (verksamhetschef) who is responsible for finances and personnel. Without the support of the head of department there will hardly be any change in recruitment. We will, therefore, invite the head of department (verksamhetschef) at the local centre to the teleconference in addition to the PI and the research nurse. Hopefully, we can work together to identify what could be done to provide more opportunities at the clinic to do research for both physicians and nurses within working hours. We have chosen a teleconference because it is time effective and less expensive than a face-to-face meeting. In addition, we hypothesised that a commitment contract would make it more personal for the local centre.
We have followed the 2013 SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) Checklist  in conjugation with the 2013 SPIRIT explanation and elaboration guidance for protocols of clinical trials  (Additional file 1).
Objectives of the study
The primary objective of this study is to investigate whether a structured teleconference re-visit with the study personnel at the centres, accompanied by a commitment contract, can enhance recruitment by 20% during 60 days post intervention, compared with 60 days pre-intervention, in an ongoing RCT.
Recruitment rate 61–120 days post teleconference
We will compare the recruitment 60 days post teleconference with a baseline inclusion from 1 Sep 2017 to 31 Oct 2017 for all centres. The purpose is to see if there is any bias or impact during the course of the study
The secondary objective must be seen as exploratory due to low power.
Does a structured teleconference re-visit with the study personnel (PI, at least one research nurse, and the head of department) at the centres, accompanied by a commitment contract, enhance recruitment by 20% during 60 days post intervention, compared with 60 days pre-intervention in the EFFECTS study?
The rationale for the trial design
We have chosen the stepped-wedge cluster randomised study design  for three reasons. First, it is not possible for us to carry out the intervention at 14–15 centres at the same time. Second, we believe that all medium and low recruiting centres could gain from the intervention, and in a stepped-wedge cluster design all centres are exposed. Every step provides before and after observations, and every step switches from control to become exposed to the intervention. Third, we have noticed a seasonal variation in recruitment. During the Christmas and Easter holidays, and especially during the summer, recruitment is falling. This intervention gives a realistic view of recruitment throughout the whole year. To the best of our knowledge, only one randomised stepped-wedge study in the field of stroke has been done .
EFFECTS has been running for almost 3 years, and we know the recruitment rate per centre and month. Initially we had 35 centres. Three centres – Karolinska Hospital Huddinge, Visby General Hospital and Högsbo Rehabilitation Hospital – have been closed due to low recruitment mainly because of a lack of PI. Of the 32 centres, we have identified five centres that have achieved our goal, that is recruiting two or more patients per month. They are the top recruiters: Danderyd Hospital, Karolinska University Hospital Solna, Skaraborg Hospital Skövde, Mora General Hospital and Sundsvall Hospital. We will not intervene at these centres because we believe that they have reached their full potential and the intervention is too weak for them. Not including the top recruiters, this leaves us with 27 centres in this study.
Figure 1 shows a Consolidated Standards of Reporting Trials (CONSORT) flow diagram  of the study. Hence, ERUTECC is a randomised, stepped-wedge cluster design  study. We made some minor changes to the CONSORT flow diagram layout.
We will use a randomised, stepped-wedge cluster design, where every step provides data before and after intervention, but not at the same point in time.
Figure 2 illustrates the stepped-wedge cluster study in our study. As the name indicates, the intervention has 11 different steps, and the schema takes the form of a wedge. Figure 3 is a schematic diagram of the time schedule of enrolment, interventions (including any run-ins and washouts) and assessments for the participating centre.
In ERUTECC, all centres have a 60-day running-in period and a 60-day post-intervention period. Our plan is to start in September 2017 and finish in October 2018.
The 27 sites will be divided into two categories: medium and low recruiters. The rationale for this is that we do not want to risk all medium recruiters falling into the same step, for example the summer period, which usually a low-recruiting period. The centre will be randomised in terms of the order in which intervention will be performed, leading to (at least) one medium and (at least) one low recruiter in each of the 11 steps (Fig. 2).
All centres in the EFFECTS study, their classification, type and numbers of patients are listed in Table 1.
Active centre in the EFFECTS study. We will invite all the study personnel at each centre. Study personnel are defined as all persons listed at the delegation list at the time for the invitation. For the meeting to happen, at least the PI, one research nurse and the head of department at the centre/hospital/unit must attend the meeting (n = 3).
Top recruiting centre in the EFFECTS study, i.e. Danderyd Hospital, Karolinska University Hospital Solna, Sundsvall Hospital, Mora General Hospital or Skaraborg Hospital Skövde.
Preparation before the intervention
This is what we will do before the intervention (teleconference):
One person, i.e. the trial manager, trial manager assistant or a PhD student, will contact the local PI or the research nurse approximately 2–3 weeks before a planned meeting and suggest three possible dates for a 1-h meeting. We will schedule the meeting via email or using a Doodle
A document is signed in which the PI consents to participate in this intervention study. In this document, the PI also gives a relevant mobile phone number that we can use to get in touch and send text messages
One week before the meeting, an email with the agenda and PowerPoint presentation attached will be sent to all participants
One day before, a text message and an email will be sent to all participants as a reminder of the meeting
The intervention – a structured teleconference
This is a teleconference between the chief investigator (CI) plus the trial manager and the study personnel. The meeting requires that at least the PI, one research nurse and the head of department (verksamhetschef) must attend the meeting. If they are not all able to attend, the meeting will be rescheduled. Ideally, as many members as possible listed on the delegation list will attend the meeting.
(a) Opening of the meeting (1 min,). Chair: trial manager. Secretary: chief investigator. Keeping track of the time: chief investigator
(b) Presentation of all at the meeting (2 min, all)
(c) Presentation of EFFECTS, PowerPoint (4 min, chief investigator)
The rationale of the study (one slide)
An update of overall recruitment (one slide)
What we need to do – our aim (one slide)
An update of recruitment at the local site (one slide)
Discussion of local barriers (5–7 min, all)
What can we do at our local centre? (5–7 min, all)
Discussion with the head of department about barriers and what can be done (5 min, all)
Where do we go from here? Formulate a commitment contract, minimum one item, maximum three items (5–7 min, trial manager)
Closing and summary of the meeting (2 min, trial manager)
Post meeting agenda
Sending out the summary of the meeting and the Commitment Contract to the PI to sign and send back to the Trial Office
Sending out a text message every Monday to the PI and research nurse during the whole period as a friendly reminder
Refusing to participate in the study
If a centre refuses to participate in the study, the reason for this is noted. We will include the centre as ‘intention-to-treat’.
First, we excluded the top recruiting centres. Second, the remaining centres were categorised as low or medium recruiters. Third, in each category (low and medium) the order of the intervention was randomised using a computer-generated allocation sequence using SAS version 9:4 by our statistician, PN. Neither the intervention nor the order of the intervention is communicated in advance. The intervention in known by the Steering Committee, ACL (author of this manuscript) and the Regional Ethical Committee, and is not communicated to the centres. The order of the allocation is known by three persons (PN, EI and EL), and is kept in an Excel file behind a secure firewall at Stockholm County Council. The centre will be contacted by the trial manager (EI) 3–5 weeks before the planned intervention. For obvious reasons, the intervention is not blinded.
Sample size and randomisation
The study has been running for almost 3 years and we know the recruitment rate per centre and month. Among the 32 centres in EFFECTS, we have identified five centres that have achieved our goal, i.e. recruiting two or more patients per month. These are the top recruiters (Danderyd, Karolinska Solna, Skövde, Sundsvall and Mora). We will not intervene with these centres because we believe that they have reached their full potential and the intervention is too weak for them. Not including the top recruiters leaves us with 27 centres in this study.
The participants in the EFFECTS study are not aware of the embedded study. We will not mention the intervention or in what order we will do the intervention outside the group responsible for ERUTECC. For obvious reasons, there is no blinding of the intervention. The centres will not be informed that we are measuring numbers of randomised patients before and after the teleconference, but they are fully aware that we want to enhance recruitment. The exact numbers of recruitments per centre has been available in the public domain through a link that has been updated in real time since the start of the EFFECTS study.
We will compare the numbers of included individuals 60 days before the teleconference with the numbers of subjects 60 days post intervention. The null hypothesis is that there will be no difference before and after. We consider a 20% increase in recruitment rate as clinical relevant, although it is arbitrarily chosen.
Sixty days pre-teleconference: 60 individuals
Sixty days post-teleconference: 78 individuals
That is, 78/60 = 1.3; a 30% increase in recruitment
In EFFECTS, we have a screening list in which we note all eligible individuals who have been considered as candidates for EFFECTS. If these patients are not part of the study, the reason is noted. Usually the reasons are administrative and non-willingness. We will compare the numbers of randomised patients with the eligible patients on the screening list.
The outcome of the study is the number of included patients per centre. Inclusion is available through our electronic randomisation system, and we will keep a separate log for every teleconference. If a centre refuses to be part of ERUTECC, we will still include the centre in the analysis (intention-to-treat). In addition, we will also do a ‘per-protocol analysis’.
Planned subgroup analyses:
Are there any differences in recruitment rate between a medium recruiting centre versus a low recruiting centre?
To what extent does the size of the stroke unit contribute to the number and percentage of patients included? Are there any differences between large stroke units versus small stroke units?
Are there any differences between stroke units versus rehabilitation centres?
Are there any differences between university hospitals versus non-university hospitals?
Are there any differences between experienced centres versus non-experienced centres?
We aim to start this study in September 2017. At that time, we will have 27 active centres, not including the five top recruiters.
Explanation of the randomised, stepped-wedge design
Step 1 starts with a 60-day running-in period beginning in September 2017, and consists of at least one medium and one low recruiting centre. The teleconference is performed at the end of October 2017, and the observation follows 60 days post intervention
Step 2 starts with a 60-day running-in period beginning in October 2017, and consists of at least one medium and one low recruiting centre. The teleconference is performed at the end of November 2017, and the observation follows 60 days post intervention
It is hard to anticipate any harm from ERUTECC. The host trial, EFFECTS, has specific monitoring performed by the Karolinska Trial Alliance. The monitor is independent and the Karolinska Trial Alliance follows a specific monitor plan, which, for example, checks every patient consent. The participants in ERUTECC will received no extra benefits for being part of the study and there will be no compensation for those who claim that they have suffered harm from trial participation.
It is possible that the intervention will develop during the course of the study. At the beginning we will have a clear agenda, but it is possible that we will learn through the process, and that the intervention will become a little different
It is also possible that the participants at the centres that have not yet been intervened with will find out about the interventions and will change their pattern of behaviour before the intervention takes place
The organisation of the intervention will be challenging because it involves more than 27 centres over a period of 1 year
At some centres, the head of the department will not be able to join during the structured telephone conference
It is possible some centres will refuse to be a part of the intervention and this will interfere with the results
Discussion and generalisability
EFFECTS is a pragmatic study of stroke and the largest RCT study of stroke in Sweden. The result from this embedded study could probably be generalised to high-income countries, like Sweden. The result could be useful in clinical settings outside the field of stroke, and if our study is positive, the results could be applicable to a wide range of RCT studies. The study will add knowledge about the management of RCT studies and recruitment.
One limitation is that we will not include the top recruiters. However, we believe that the high recruiting centres have reached their maximum level of recruitment and the intervention will only have a minor effect
It is possible that the intervention is too weak to have positive results. After all, we are trying to change the pattern of behaviour for over 60 persons and behaviour change is one of the hardest things to accomplish
Since we started the EFFECTS study, we have already tried different things to identify barriers and find ways to enhance recruitment, so it may be that there is nothing more to be done
We are planning to carry out multiple sub-group analyses. The results must be interpreted with caution
The main study – EFFECTS – included its first patient on 20 October 2014, and as of 31 October 2017, 881 patients have been included. The last patient is estimated to be recruited in March 2019, with the last follow-up 1 year later. The ERUTECC will start in November 2017 (Fig. 2) and continue for 1 year.
Consolidated Standards of Reporting Trials
Efficacy oF Fluoxetine – a randomisEd Controlled Trial in Stroke
Enhancing Recruitment Using Teleconference and Commitment Contract
Randomised controlled trial
Standard Protocol Items: Recommendations for Interventional Trials
Study Within a Trial repository
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We thank Professor Rustam Al-Shahi Salman, University of Edinburgh and Professor Shaun Treweek, University of Aberdeen, for their valuable comments on the study. We thank the EFFECTS collaborators as well as all patients participating in the EFFECTS study.
This study will be conducted within the funding of the EFFECTS study. In addition, we are also applying for extra grants. EFFECTS has currently received grants from the Swedish Medical Council, the Swedish Brain Foundation, the Swedish Heart-Lung Foundation, King Gustav V and Queen Victoria’s Foundation of Freemasons, the Swedish Stroke Association and the Swedish Society of Medicine. All funders are non-commercial, with none from industry. None of the funders nor the sponsor had any role in the design of this study and will not have any role during its execution, analyses, interpretation of the data or decision to submit results.
Availability of data and materials
The datasets for ERUTECC will be available from the corresponding author on reasonable request.
The sponsor is Karolinska Institutet, Danderyd Hospital, 182 88 Stockholm, Sweden. The sponsor’s representative is Erik Lundström (corresponding author).
ERUTECC is an embedded study of the EFFECTS study and, as such, we have not set up any separate steering committee, data management or data management committee for ERUTECC. The following applies to the both EFFECTS and the embedded study, ERUTECC.
The coordination centre is located at Karolinska Institutet, Danderyd Hospital and those responsible for day-to-day management are Chief Investigator Erik Lundström, Trial Manager Eva Isaksson and Trial Manager Assistant Nina Greilert.
The Steering Committee has the task of following the development of the study, assisting the CI with advice and support when needed, and helping to solve problems. The Steering Committee is also responsible for ensuring that the protocol for the study is followed. The Steering Committee is responsible for:
Policies, superior organisational issues and any technical issues
The report of the Data Management Committee will be received by the Steering Committee
Monitoring finances; however, Karolinska Institutet is the financial manager and manages funds
Overseeing staff; however, Karolinska Institutet has personnel responsibility
Considering the need for any protocol changes
If any sub-studies are to be done within the framework of the main study, this should be presented orally first. If the Steering Committee considers the study to be feasible and scientifically sound, and that it does not affect the main study, a written project report may be submitted. This will be approved by the Steering Committee before any application is sent. A signed (by the Chair of the Steering Committee after approval by the Steering Committee) project plan will be filed at Karolinska Institutet. When submitting an application for ethical approval or funds, the Chair of the Steering Committee and the CI will be informed of this before submission. No changes may be made to an approved protocol without this being approved and signed in accordance with the previous description.
The Steering Committee will ensure that a good publication policy is applied to the protocol which states that publications are prepared by persons approved by the Steering Committee. The study is dependent on collaboration with a large number of physicians, nurses, patients and relatives. Those included in the local centre (which are on the delegation list) will be included in a list. The publication is prepared by a writing committee. We follow the current International Committee of Medical Journals Editors’ recommendations .
Members of the Steering Committee
The Steering Committee consists of Professor Katharina Stibrant-Sunnerhagen (Chair), Professor Per Wester, Professor Bo Norrving, Professor Håkan Wallén, Senior Professor Jörgen Borg, Senior Associate Professor Björn Mårtensson, Associate Professor/statistician Per Näsman, Chief Investigator/Associate Professor Erik Lundström and Trial Manager Eva Isaksson.
The task of data management is divided between the centres, Karolinska Institutet, Karolinska Trial Alliance and EDC Scandinavia AB personnel, and all parties will ensure that qualified staff are available.
The responsibilities are divided up as follows:
|Database design||EDC Scandinavia|
|e-CRF design||EDC Scandinavia, Karolinska Institutet and Karolinska Trial Alliance|
|Server management||EDC Scandinavia|
|Data collection||Centre and Karolinska Institutet|
|Data manager||EDC Scandinavia|
|Case Report Form (CRF) annotation||Centre, Karolinska Institutet and Karolinska Trial Alliance|
|Data entry||Centre, Karolinska Institutet and Karolinska Trial Alliance (only central 6 and 12 months)|
|Monitoring||Karolinska Trial Alliance|
|Source data verifications||Karolinska Trial Alliance|
|Issue and resolve data correction forms||Karolinska Institutet and Karolinska Trial Alliance|
|Medical coding||Karolinska Institutet|
|Data validation||EDC Scandinavia and Karolinska Institutet|
|Discrepancy management||Centre, Karolinska Institutet and Karolinska Trial Alliance|
|Database lock. The database will be preserved according to Karolinska Institutet’s rules, the electronic notebook ||EDC Scandinavia|
Data Monitoring Committee (DMC)
The Data Monitoring Committee (DMC) will independently monitor patient safety and efficacy information, and will conduct the study, during the period of the trial. The DMC comprises two physicians with stroke expertise: Senior Professor Kjell Asplund (Chair), Senior Associate Professor Kerstin Hulter Åsberg and a biostatistician, Anders Ljungström.
DMC members will not be involved as PIs or sub-investigators in the study. In addition, DMC members must not have a conflict of interest that would bias their review of trial data (e.g. DMC members must not have a financial interest that could be substantially affected by the outcome of the study, strong views on the relative merits of the study drug, relationships with individuals in trial leadership positions that could be considered reasonably likely to affect their objectivity, or involvement in any potential competing trial).
The unblinded statistician, a member of the DMC, will generate data and reports for the DMC to review. The CI will serve as a primary contact person for the DMC and DMC issues.
As a rule, DMC contacts and consultants must not attend closed sessions of DMC data.
The DMC Chair will ensure that DMC contacts and consultants are not inappropriately exposed to unblinded data made available to the DMC.
The DMC is an independent expert advisory group commissioned and charged with responsibility for evaluating cumulative safety, efficacy and other clinical trial data at regular intervals. As such, the primary objective of the DMC is to monitor the safety of the subjects in the study by reviewing the available clinical data at scheduled time points including at least yearly meetings (which may be face to face or via teleconference) and on an ad hoc basis as needed.
After the review of each data report has been completed, the DMC Chair will provide the official DMC recommendation to the sponsor, the CI and the Chair of the Steering Committee regarding the appropriateness of continuing the study, from a safety and efficacy perspective, as well as any other recommendations relevant to study conduct and/or patient safety.
Specifically, the DMC members are authorised and expected to perform the following functions:
Safeguard the interests of trial participants
Provide approval for, and operate in, accordance with the specifications outlined in this DMC Charter
Monitor the safety and efficacy of the trial intervention, through scheduled review of accumulating clinical data from the ongoing clinical trial and taking into account information from external sources
Consider the need for additional unscheduled reviews of study data
Review and evaluate the content of all unblinded data reports received
Ensure the confidentiality of all information received relating to the trial
In the event of further funding being required, to provide the Steering Committee and funder(s) with appropriate information and advice on the data gathered to date in a manner that will as far as possible protect the integrity of the study
Participate in and vote on DMC recommendations, bearing in mind the fact that ethical considerations are of prime importance
Make clear recommendations to the Steering Committee, with the Steering Committee Chair as the principal contact
The DMC will review safety outcomes, including serious adverse events. Review of safety data should occur after 150, 300, 600, 900 and 1200 patients’ 6-month follow-up data. No formal boundaries will be used for terminating the study for safety reasons, but clear and consistent evidence of net harm that overrides any benefit should be apparent
A formal interim analysis to assess efficacy will occur when approximately 67% of the planned primary efficacy events have accrued. The DMC may recommend early termination of the trial for overwhelming superiority of fluoxetine over control. A modified Haybittle-Peto monitoring boundary will be used as a guideline. If the primary efficacy comparison exceeds four standard errors in value, the DMC will initiate another interim analysis to be performed a minimum of 3 months later. If the monitoring boundary remains crossed, the DMC may recommend that the trial be terminated early for overwhelming superior efficacy of fluoxetine. No adjustment of the significance level for the final analysis is required.
The DMC will not be asked to make any recommendations on whether the trial should be stopped on the basis of futility, i.e. that the trial – if it recruits to its target sample size – is unlikely to demonstrate a benefit from the trial of fluoxetine.
Throughout the trial, the DMC Chair will take responsibility for the Committee’s operation and will be authorised and charged with the following responsibilities:
Chair DMC data review meetings
Ensure that all relevant data have been reviewed by the DMC members and that all issues have been addressed
Ensure that blinded individuals (i.e. the DMC coordinator, DMC contacts and DMC consultants) are not inappropriately exposed to confidential and/or unblinded data
Ensure that only the members of the DMC are present during DMC deliberations, when DMC recommendations are discussed and DMC voting procedures are conducted
Ensure the generation of confidential, written minutes of all closed sessions of any DMC Meetings and maintain these minutes as confidential to DMC members only, until the final (end of study) database lock is complete
Ensure DMC approval of minutes of open and final sessions of all DMC meetings
Communicate, author, sign and provide the official, final recommendations of the DMC within specified timelines and according to the specifications outlined in this charter. If the DMC is divided in opinion on any major issue affecting the DMC’s recommendation to the sponsor and EFFECTS Steering Committee, the DMC Chair is responsible for assembling and presenting the majority and dissenting opinions for all recommendations considered
Arrange for consultation(s) and/or request additional data, as deemed necessary
If deemed appropriate by the DMC, at appropriate intervals, arrange a teleconference meeting with the Chairs of the DMCs for the FOCUS (Professor Peter Langhorne) and AFFINITY (Professor Robert Herbert, Australia) trials. If necessary, to discuss accumulating data in strict confidence and any implications for the continuation of each of the trials. Each Chair may then subsequently need to consider whether to arrange a meeting of their respective trial DCM to discuss any issues that may arise from this liaison group
Maintain a secure central file of all data outputs received for DMC review and all minutes of all sessions of DMC meetings. Provide a copy of this file to the sponsor, through the CI, once the final (end of study) database lock is complete
Principal investigator at each centre
At each participating centre a PI will be identified, to be responsible for identification, recruitment, data collection and completion of CRFs, along with follow-up of study patients and adherence to the study protocol and the investigators’ brochure. The PI will not be part of the Steering Committee.
Ethics approval and consent to participate
Ethics approval for ERUTECC, Stockholm Ethical Review Board, Sweden on 8 August 2017, ref. number 2017/1285-31/1. We plan to communicate important protocol modifications (e.g. changes to eligibility criteria, outcomes, analyses) to relevant parties (e.g. investigators, REC/IRBs, trial participants, trial registries, journals and regulators). The PI at each centre has to give their oral and written consent to participate in ERUTECC. If a PI refuses to participate, the reason for this is noted. We will include the centre as intention-to-treat.
Consent for publication
The authors declare that they have no competing interests.
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Lundström, E., Isaksson, E., Wester, P. et al. Enhancing Recruitment Using Teleconference and Commitment Contract (ERUTECC): study protocol for a randomised, stepped-wedge cluster trial within the EFFECTS trial. Trials 19, 14 (2018) doi:10.1186/s13063-017-2367-8
- Randomised controlled trial
- Randomised stepped-wedge cluster trial