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Core outcomes set for research on the treatment of opioid use disorder (COS-OUD): the National Institute on Drug Abuse Clinical Trials Network protocol for an e-Delphi consensus study
Trials volume 22, Article number: 102 (2021)
A lack of consensus on the optimal outcome measures to assess the efficacy and effectiveness of interventions for the treatment of opioid use disorder (OUD) has hampered the pooling of research data for evidence synthesis and clinical guidelines. A core outcome set (COS) is a minimum set of outcome measures that are recommended for all studies of a particular condition. The National Drug Abuse Treatment Clinical Trials Network (CTN) Core Outcome Set for OUD (COS-OUD) is a development study to identify core constructs, meaningful outcomes, and their optimal measurement for all efficacy and effectiveness studies of OUD treatment and service delivery.
Overseen by an expert workgroup, a modified, stepwise, e-Delphi methodology will be used to gain consensus among a panel of clinical practitioners and researchers involved in the treatment of OUD, who are members of the CTN. Sequential rounds of anonymous, online questionnaires will be used to identify, rate the importance of, and refine a core outcome set. A consensus threshold will be achieved if at least 70% of the panel rate the measure as critical for inclusion in the COS-OUD. Where consensus is not reached or there are suggestions for new measures, these will be brought forward to a further round of review prior to a consensus meeting. Products from this study will be communicated via peer-reviewed scientific journals and conferences.
This initiative will develop a COS for OUD intervention trials, treatment studies, and service delivery and will support the pooling of research and clinical practice data and efforts to develop measurement-based care within the OUD treatment cascade.
Opioid use disorder (OUD) is a debilitating biobehavioral condition  with major social overlays  that is associated with a substantial global burden of disease  and, in several countries, a sharp recent increase in overdose fatalities [3, 4].
To address the opioid epidemic, ongoing international research efforts aim to create innovations with front-line opioid agonist, partial agonist/antagonist, and antagonist therapies for OUD. These include new developments of extended-release formulations of some medicines, evaluations of adjunctive psychosocial interventions, and applied efforts to expand patient access in priority healthcare settings .
In the past four decades, evidence for the efficacy of the medication and psychosocial treatments for OUD has accumulated from randomized controlled trials and observational studies using one or more of the following direct or indirect assessments of benefit: patient-reported outcomes (PRO), clinician-reported (ClinRO), observer-reported (ObsRO), or performance outcomes (PerfO). Measures have included self-reported drug use, problem checklists, personal functioning, biomarkers, and indicators of treatment retention and completion. However, no consensus exists on the optimal ways of measuring clinical benefit and other patient outcomes. Accordingly, clinical trials use a wide array of measures and operational definitions of key outcomes, limiting the ability to make direct comparisons across studies, to aggregate data across studies, and to allow for benchmarking.
Established in 1999, the National Drug Abuse Treatment Clinical Trials Network (CTN) is a network of university- and health system-based research groups and healthcare service providers that collaborate on research on OUD and other substance use disorders, and coordinates data and discovery across a multitude of trials. De-identified research data from these completed trials are distributed to the scientific community and the public at large through an electronic repository, the National Institute on Drug Abuse Data Share website [6, 7]. One feature of the website is that it displays the assessments used in each study, by construct-based category, and identifies studies that use similar assessments. This, in part, is meant to encourage the use of common instruments in future studies examining similar constructs (e.g., depression).
In 2000, in a more targeted effort of harmonization, the CTN recommended a common assessment battery for research . This was subsequently included in 21 randomized controlled studies, but feedback from patients, service providers, and researchers concluded that the battery was administratively burdensome and infeasible in practice, largely because of the number of items . In 2009, a CTN taskforce recommended a shorter set of instruments , but these were not widely or consistently adopted . Interestingly, this task force did find a desire to have a “minimum (i.e., core) data set as a standard” S2: . In 2014, a public portal was launched providing access to 18 recommended screening and clinical research instruments , with integration support for inclusion in clinical research and electronic health records (EHR) [13, 14]. In 2019, the Data & Statistics Center of the CTN, under commission from the CTN Steering Committee, developed and published a battery of standardized assessments for research . The battery includes standardized forms for data gathering, measures that have been extracted from the NIH PhenX toolkit , and many other validated tools that have high relevance to drug misuse research. Overall, these prior initiatives produced highly valuable syntheses of tools and instruments, but their overall length and number of items prevent universal use as a COS.
In the era of measurement- and value-based care, key stakeholders have an increasing expectation that health care service providers incorporate standardized and clinically actionable measures in their EHRs to facilitate data pooling in healthcare systems. Several ongoing initiatives have this goal in mind, including the Patient-Reported Outcomes Measurement Information System (PROMIS), which includes over 300 measures organized in profile domains; the consensus measures for phenotypes and exposures initiative which includes approximately 800 measurement protocols in toolkits; and the Fast Healthcare Interoperability Resource (FHIR) standard for healthcare data exchange produced by the Health Level 7 international community. In a series of workshops and publications, the Food and Drug Administration has promoted clinical outcome assessments and called for greater use of patient-reported outcomes in research studies . NIDA and other federal agencies have also sought evidence of the benefits of decreased substance use short of abstinence.
In spite of these sustained and multiple ongoing efforts, implementing common measures for OUD treatment studies has been elusive. A solution to the problem of outcome measurement consensus that has gained success in many areas of medicine is to identify the absolute minimum set of measures—the so-called core outcome set (COS)—that are to be reported in all efficacy research studies on a target condition . A COS does not restrict outcome measures, and it is expected that researchers would usually need other measures to address specific study aims, but it is expected that using a COS will result in studies of higher quality, applicability, and impact. This approach provides researchers with the needed flexibility to target assessment batteries to their study aims and population of interest, while maintaining the benefits of a common assessment battery to facilitate comparison across studies and the aggregation of datasets. The Core Outcomes Measures in Effectiveness Trials (COMET) database lists preregistered COS development (http://www.comet-initiative.org).
Most COS development studies use a Delphi methodology. First developed by the RAND Corporation in the 1950s and 1960s, Delphi is a family of participatory and stepwise procedures for eliciting and refining the opinions of a panel of people who are usually experts on a particular topic. The panel consents to have their views and value judgments gathered and combined to establish a consensus on a topic of complexity where there is uncertainty, and where there are concerns that current practice or policy is an impediment to progress [19, 20]. Delphi studies follow four principles: anonymity of panel members’ responses (to mitigate against group pressure and the biasing influence of dominant viewpoints), iteration, controlled feedback, and statistical aggregation of panel responses .
Commonly, COS development studies proceed through four steps. In the first step, a concept mapping of the topic is done by a study workgroup to set the scope. A second step involves a systematic review of existing outcome measures to gather potentially relevant material. The third phase is a sequence of questionnaires (usually web-based) sent to the panel, beginning with an open-ended format to canvass a wide range of outcome options and progressing through a closed format with instructions to estimate the relevance and importance of potential measures. Removal and modifications of measures in successive rounds are done according to a predetermined criterion alongside opinion feedback. Further rounds of questionnaires are issued until a consensus is judged to have been reached by the achievement of the pre-determined agreement threshold. Finally, a consensus meeting is held to discuss the study products and resolve outstanding issues, prior to the communication of results. On completion of these four steps, results are publicized.
The need for consensus on outcome measurement for OUD research has intensified in the context of the current opioid crisis and the large number of planned OUD-related research studies at the CTN supported by the National Institutes of Health’s Helping to End Addiction Long-term (HEAL) initiative . In March 2020, with advice from the Center for Clinical Trials Network staff and leadership, a proposal was submitted to the CTN Research and Development Committee Great Lakes Node to lead a COS development study on OUD-related research. At the March 2020 CTN Steering Committee Meeting Webinar, a workgroup was formed to develop the protocol and implement the COS-OUD study. The co-authors of this manuscript constitute the workgroup. This workgroup determined the protocol for the establishment of the eDelphi panel. A subset of the workgroup also participates on the panel along with a broader group of stakeholders from within the CTN.
Aims and research questions
With only one prior OUD study registered on the COMET database, this article describes a different e-Delphi protocol for COS-OUD which has different goals than COMET protocol 1128 . The goals of this study are to identify a COS for OUD-related treatment efficacy and effectiveness research; to develop guidelines for their recording, analysis, interpretation, and communication; and to promote their use for research and clinical practice. Products from COS-OUD are also envisaged to contribute to efforts to develop measurement-based care for OUD interventions . The study will address the following four questions:
What are the core constructs or domains to be included in the COS?
What are the differences in priority and perspective between different professions?
What outcome items are rated most important?
How should outcome items be optimally defined and captured?
COMET protocol 1128 which was funded by the Canadian Institutes of Health Research in March 2018 has produced systematic reviews [25, 26], but the protocol has not produced a defined outcome set. In addition, their goal is much larger in trying to develop a comprehensive set of patient-oriented outcomes. Our aim is to establish a minimum set of key outcomes that can be used for study linkage across the OUD treatment cascade.
The COS-OUD will comprehensively cover adult OUD studies and include all interventions for the treatment of OUD including psychosocial and medical treatments of OUD covered by the mandate of the CTN [URL: https://www.drugabuse.gov/about-nida/organization/cctn/clinical-trials-network-ctn].
In the context of principles of treatment, patient involvement and low administrative burden, and informed by the COnsensus-based Standards for the selection of health Measurement INstruments (COSMIN ) and the COMET handbook , COS-OUD will be developed following the COS-STAD guideline , COS-STAP statement , and will be reported following the COS-STAR guideline . The study is registered on the COMET website [URL: http://www.comet-initiative.org/Studies/Details/1579]. The study will use an e-Delphi consensus method with data capture via web-based questionnaires, with final panel results reported anonymously.
Panel membership and recruitment
The size of a panel for the study will be determined following the principle of inclusivity. Membership of the panel will be open to employed professionals in all 18 CTN nodes who are either clinical addiction practitioners (accredited with a current license as a physician, physician assistant, psychologist, social worker, pharmacist, nurse practitioner, or nurse) or researchers and data administrators. It is anticipated that a panel size of about 40 members will be recruited. In many COS development studies, panel members are not permitted to contribute to subsequent rounds of data collection if they have not contributed to a previous round, but due to the circumstances currently taking place with the COVID-19 pandemic, we plan to relax this approach and allow for a more open process. To minimize attrition, we will clearly set out the importance of full participation and emphasize to members attrition can undermine the degree of consensus in the results. However, we will allow panel members to miss a round and will ask members who leave the study to volunteer a reason as part of efforts to assess possible validity threats to the consensus process .
Review of prior and current CTN OUD trials
As a prelude to the Delphi process, the lead team will undertake a review of past and current CTN OUD trials to assess the current state of measures. This review will be undertaken using the CTN Dissemination Library [URL: http://ctndisseminationlibrary.org/] which has all of the documentary data for the CTN and the parameters will be on treatment studies with OUD outcomes. In addition, members of the expert workgroup will undertake a scoping review to gather potential items for the COS-OUD that will be fed directly into the Delphi process. During this phase, panel members may also nominate specific items during the Delphi protocol.
Assessing domains of measurement
In addition to specific items that have the potential to serve as elements in the OUD-COS, panel members will be first asked to rank broad domains of measurement (i.e., use per unit time, craving, withdrawal) in the early rounds of reviews. These domains will be used to reflect on the relative importance of major categories of measurement. This exercise will allow the Delphi process to highlight a higher level of conceptual thinking and avoid getting too focused on representation within individual measures. The purpose of doing this before the individual item rounds of questions is to assess whether thinking about specific items changes the perceived importance of categories. Rankings data will be presented to the panel prior to each new round of questions.
Delphi questionnaire and analysis
We will use REDCap (version 6.18.1) to create web-accessible questionnaires. Each questionnaire will be online for up to 4 weeks with reminder emails sent to panel members every 7 days. In the first round, we will invite panel members to rank the importance of each outcome measure on a 1–9 scale (1–3 rated “not important for inclusion”; 4–6 rated “important but not critical”; 7–9 rated “critical for inclusion”). Percent agreement is the most commonly used method for consensus definition with thresholds ranging from 50 to 97% according to a review of Delphi studies . We will set the consensus definition at 70% or greater [34, 35].
Panel members will see the results in the second round and with eventual consensus defined as 70% (or greater) or more of the respondents scoring an outcome from 7 to 9 and fewer than 15% scoring it 1–3. This approach has an established track record of use and is recommended by the Grading of Recommendations Assessment, Development and Evaluation (GRADE) Working Group for assessing the level of importance about research evidence [https://www.gradeworkinggroup.org]. Should we have three rounds result in a lack of consensus or lack of movement toward it, then we would declare the process will be ended and the varied sides/camps will be reported.
Panel members will be asked to provide recommendations regarding any additions and/or deletions to the list of proposed items, and for any other comments/suggestions. Each questionnaire should take no more than 20–40 min to complete, with the facility to complete it over several sessions and to allow participants to review their answers before the final submission of their responses. De-identified results comprising a narrative summary of findings, comments, and suggestions will be sent to each panel member after the first round. In a second round, ambiguous items or proposals collected from the first round will be compiled (with input from the workgroup as required) before being included in the new round.
Due to COVID-19 challenges for all stakeholders, we plan to handle missing data with a relatively flexible approach. In the event that panel members fail to respond to a single survey, we plan to allow these members to join future rounds of the panel. Individual items that participants skip or opt to not respond to will be re-calculated by using a lower number of panel members thereby accounting for the lack of response.
Consensus meeting and dissemination plan
Prior to the final determination of the COS-OUD and communication of study results in a peer-reviewed academic journal, we plan to organize a webinar or face-to-face consensus meeting open to CTN nodes, service user representatives, and other key CTN stakeholders to discuss the results of the Delphi process. Depending on the state of travel related to COVID-19, the meeting may be in-person or virtual. Our plan is to have the workgroup leads (Karnik and Marsden) facilitate the meeting. The meeting will be open to all members of the CTN regardless of participation on the eDelphi panel.
This protocol describes a study to develop a COS for OUD-related treatment efficacy and effectiveness trials and allied research. The literature on OUD includes many different outcome measures leading to a lack of clarity on which outcomes are of most importance to researchers and patient stakeholders in terms of understanding experience over the treatment cascade. This in turn has impeded evidence synthesis with missed opportunities to develop pooled research data or to compare results across studies to inform treatment policy and practice.
A previous sustained effort to promote a common approach to the use of outcomes measures has favored a multi-dimensional outcome instrument approach . This study will take an alternative strategy with the goal of identifying a minimum set of outcome items that can be used in all efficacy and effectiveness studies.
At the point of manuscript submission, a proposal for the study had been approved, a workgroup had been formed, Institutional Review Board clearance had been received, and the study had been registered with the COMET website. The first phase of this Delphi process is now underway along with the recruitment of the panel.
Availability of data and materials
Survey data from the eDelphi process will be archived at Rush University for a period of 5 years. Investigators interested in reviewing the survey data directly may do so by contacting staff at the Great Lakes Node of the National Drug Abuse Treatment Clinical Trials Network.
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The authors gratefully acknowledge the assistance of Mr. Randy Boley and Mr. Connor McCluskey in the preparation of background materials and RedCap surveys for this project.
Resource support for this study was provided by CTN Great Lakes Node at Rush University (NIH Grant UG1-DA049467). We would like to thank the members of the NIDA Center for Clinical Trials Network (CCTN) and CTN for their input to this consensus development study. CCTN scientific staff participate as members of the workgroup and have a role in the study implementation, review, and writing of the manuscript. The funder has no direct role in the study design, implementation, and manuscript preparation. The content is solely the responsibility of the authors and does not necessarily represent the official view of the National Institute on Drug Abuse.
Ethics approval and consent to participate
The protocol for COS-OUD was reviewed by the Rush University Institutional Review Board and a determination of exception from the formal review was granted on 6 April 2020. All panel members will complete a consent and declaration of interests form. These materials and all data gathered by the study will be kept at the offices of the CTN Great Lakes Node at Rush University on password-encrypted electronic storage. Only researchers named on the protocol approved by the IRB will have access to study data. Study data will be kept for 5 years in accordance with the NIH policy and then archived.
Consent for publication
All workgroup members and co-authors have given consent for publication.
NK, in addition to the support outlined above, is supported by grants from the National Center for Advancing Translational Science (UL1-TR002389, KL2-TR002387), the National Institute on Drug Abuse (R01-DA041071, R01-DA051464), the Substance Abuse Mental Health Services Administration (H79-SM082299), and the National Institute on Mental Health (R01-MH117168).
MC is supported by a grant from the National Institute on Drug Abuse (UG1DA049435).
CC is supported by grants and contracts from the National Institute on Drug Abuse (UG1DA040314, R01DA047405) and the Food and Drug Administration. Dr. Campbell has received support through her institution from the Industry PMR Consortium, a consortium of companies working together to conduct postmarketing studies required by the Food and Drug Administration that assess known risks related to opioid analgesic use.
DF is supported by a grant from the National Institute on Drug Abuse (5UG1DA015831).
UG is an employee of the Center for the Clinical Trials Network of NIDA, the funding agency for the CTN. The opinions in this manuscript are those of the authors and do not represent the official position of the National Institutes of Health.
KH is supported by the Emmes Data and Statistics Center, which is funded by a contract from the National Institute on Drug Abuse (75N95019D00013).
YH is supported by grants from the National Institute on Drug Abuse (UG1DA049435, R21/R33 DA042280, R21/R33 DA045844).
KMcH is supported by grants from the National Institute on Drug Abuse (R21DA046937, R21DA046521, R01 DA045632, UG1DA015831).
SMM is supported by grants and contracts from the National Institute on Drug Abuse (R01DA046721, P30DA040500, R01DA044878, R01DA046527, R01DA045042, UG1DA040314, U01DA047408, UG1DA013732, UG1DA013035, UG1DA015831, UM1DA049412, UG1DA050071, UG1DA050077, UG1DA050067), the National Institute of Mental Health (R01MH118107), the National Institute on Alcohol Abuse and Alcoholism (R01AA020248), the Centers for Disease Control and Prevention (R01CE002999), and the California Department of Health Care Services.
SMcP is supported by NIH grants P20MD006871, UG1DA013714, R01EY027476, N44DA162246, R01AA022070, R01AA020248, P60AA026112, R41AA026793, N44DA171210, and R01AG042467; VA grant I01HX002518; and CDC grant 75D301-19-Q-69877.
LJM is supported by grants from the National Institute on Drug Abuse (UG1DA049435, R21/R33DA042280, R21/R33DA045844, R01DA045162).
LM is an employee of the Center for the Clinical Trials Network of NIDA, the funding agency for the CTN. The opinions in this manuscript are those of the authors and do not represent the official position of the National Institutes of Health.
LW is supported by grants and contract from the National Institute on Drug Abuse (UG1DA040317), National Institute on Minority Health and Health Disparities (R01MD007658), Patient-Centered Outcomes Research Institute, and Centers for Disease Control and Prevention.
DSB is supported by the Emmes Clinical Coordinating Center, which is funded by a contract from the National Institute on Drug Abuse HHSN271201500065C.
MS is supported by grants from the National Institute on Drug Abuse (UG1 DA013035-18, 1UM3 1DA049415-01) and SAMSHA (H79 TI080816-01).
RPS is supported by grants from the National Institute on Drug Abuse (UG1DA013034, 1U01DA046910, 1U01DA047982, 3U01DA046910, 1R01DA043476-02S1). He has served as a consultant for Verily Life Sciences, Ltd.
KS is supported by the National Institute of Drug Abuse’s National Drug Abuse Treatment Clinical Trials Network (CTN) Pacific Northwest Node (3 UG1DA013714).
KW is supported by grants from the National Institute of Drug Use: R34DA046950, R34DA047492, 1R01DA046226, 1UG1DA049435; NIAAA: R34AA025480; PCORI: OBOT-2018C2-1287; NIMH: 1UF1MH121954-01.
JM is supported by the Center for the Clinical Trials Network. He is senior academic advisor at the Alcohol, Drugs, Tobacco and Justice Division of Health Improvement at Public Health England. He declares an unrestricted research grant from Indivior at King’s College London and South London and Maudsley NHS Trust, UK, for a multi-center, randomized controlled trial study of injectable depot buprenorphine for OUD.
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Karnik, N.S., Campbell, C.I., Curtis, M.E. et al. Core outcomes set for research on the treatment of opioid use disorder (COS-OUD): the National Institute on Drug Abuse Clinical Trials Network protocol for an e-Delphi consensus study. Trials 22, 102 (2021). https://doi.org/10.1186/s13063-021-05051-9
- Core outcome set
- Opioid use disorder
- Patient-reported outcomes
- E-Delphi survey
- Outcome reporting