The development of a national bilingual cross-sectional questionnaire on attitudes towards supervised consumption sites and e-health overdose response interventions in Canada: The Canadian National Questionnaire on Overdose Monitoring (CNQOM)

ABSTRACT

Background Supervised consumption sites (SCSs) and overdose response hotlines/applications (ORHAs) are harm reduction interventions aimed at reducing fatal overdose mortality. Little is known about key informant perspectives regarding these services. Herein, our objective is to describe the process of developing, testing, and distributing a novel national online questionnaire to measure perspectives and attitudes towards SCS and ORHAs among key informants in Canada.

Methods A bilingual online instrument (the Canadian National Questionnaire on Overdose Monitoring, CNQOM) was developed, pilot tested and revised with the aim of ensuring content and construct validity. Questionnaire respondents were recruited nationally from four key informant groups (People Who Use Substances, health professionals, emergency responders, and the general public) using a mix of purposive and representative sampling strategies. Respondents came from every province and territory in Canada, and respondents from the general public were proportionally represented. A stepwise response validation approach was used to remove invalid questionnaire responses. Test-retest reliability of instrument questions was assessed using Spearman’s Rank Correlation, the Wilcoxon Rank Sum Test, and Cohen’s Kappa.

Results A total of 4,445 valid responses was obtained from the four key informant groups following data cleaning. Test-retest reliability of instrument questions demonstrated slight to substantial stability in responses.

Discussion The CNQOM is the first online questionnaire in Canada designed to capture perspectives and attitudes towards SCSs and ORHAs among diverse key informant groups. Our questionnaire was administered to a large, geographically diverse sample and designed to capture the perspectives of four key informant groups. Lower than expected test-retest reliability may be explained by lack of participant familiarity with SCS and especially ORHAs and the impersonal nature of the instrument content among some respondents. Future work will elucidate key informant perspectives on these services based on the data.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study received financial backing from Health Canada's Substance Use and Addictions Program (SUAP) [Agreement No. 2122-HQ-000021] and the Canadian Institutes of Health Research (CIHR) [Funding Reference No. 181006]. Both funding sources were received by M.G. SUAP and CIHR were not involved in any aspect of the study's design, data collection, data analysis, result interpretation, or the decision to publish the findings. The opinions presented in this paper are solely those of the authors and do not necessarily align with the views of Health Canada. B.S. and D.V. received payment as research assistants from the listed funding sources. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study was approved by the University of Calgary's Conjoint Health Research Ethics Board (CHREB; REB #21-1646).

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

Data cannot be shared publicly because of University of Calgary ethics rules. Data are available from the University of Calgary for researchers who meet the criteria for access to confidential data.

Comments (0)

No login
gif