Results from the BETTER WISE trial: a pragmatic cluster two arm parallel randomized controlled trial for primary prevention and screening in primary care during the COVID-19 pandemic

dc.contributor.authorManca, Donna P.
dc.contributor.authorFernandes, Carolina
dc.contributor.authorLofters, Aisha
dc.contributor.authorAubrey-Bassler, Kris
dc.contributor.authorShea-Budgell, Melissa
dc.contributor.authorCampbell-Scherer, Denise
dc.contributor.authorSopcak, Nicolette
dc.contributor.authorMeaney, Christopher
dc.contributor.authorMoineddin, Rahim
dc.contributor.authorMcBrien, Kerry
dc.contributor.authorKrueger, Paul
dc.contributor.authorWong, Tracy
dc.contributor.authorGrunfeld, Eva
dc.date.accessioned2023-10-01T00:02:51Z
dc.date.available2023-10-01T00:02:51Z
dc.date.issued2023-09-28
dc.date.updated2023-10-01T00:02:50Z
dc.description.abstractAbstract Background Cancer and chronic diseases are a major cost to the healthcare system and multidisciplinary models with access to prevention and screening resources have demonstrated improvements in chronic disease management and prevention. Research demonstrated that a trained Prevention Practitioner (PP) in multidisciplinary team settings can improve achievement of patient level prevention and screening actions seven months after the intervention. Methods We tested the effectiveness of the PP intervention in a pragmatic two-arm cluster randomized controlled trial. Patients aged 40–65 were randomized at the physician level to an intervention group or to a wait-list control group. The intervention consisted of a patient visit with a PP. The PP received training in prevention and screening and use of the BETTER WISE tool kit. The effectiveness of the intervention was assessed using a composite outcome of the proportion of the eligible prevention and screening actions achieved between intervention and control groups at 12-months. Results Fifty-nine physicians were recruited in Alberta, Ontario, and Newfoundland and Labrador. Of the 1,005 patients enrolled, 733 (72.9%) completed the 12-month analysis. The COVID-19 pandemic occurred during the study time frame at which time nonessential prevention and screening services were not available and in-person visits with the PP were not allowed. Many patients and sites did not receive the intervention as planned. The mean composite score was not significantly higher in patients receiving the PP intervention as compared to the control group. To understand the impact of COVID on the project, we also considered a subset of patients who had received the intervention and who attended the 12-month follow-up visit before COVID-19. This assessment demonstrated the effectiveness of the BETTER visits, similar to the findings in previous BETTER studies. Conclusions We did not observe an improvement in cancer and chronic disease prevention and screening (CCDPS) outcomes at 12 months after a BETTER WISE prevention visit: due to the COVID-19 pandemic, the study was not implemented as planned. Though benefits were described in those who received the intervention before COVID-19, the sample size was too small to make conclusions. This study may be a harbinger of a substantial decrease and delay in CCDPS activities under COVID restrictions. Trial registration ISRCTN21333761. Registered on 19/12/2016. http://www.isrctn.com/ISRCTN21333761 .
dc.identifier.citationBMC Primary Care. 2023 Sep 28;24(1):200
dc.identifier.urihttps://doi.org/10.1186/s12875-023-02159-6
dc.identifier.urihttps://hdl.handle.net/1880/117313
dc.language.rfc3066en
dc.rights.holderBioMed Central Ltd., part of Springer Nature
dc.titleResults from the BETTER WISE trial: a pragmatic cluster two arm parallel randomized controlled trial for primary prevention and screening in primary care during the COVID-19 pandemic
dc.typeJournal Article
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
12875_2023_Article_2159.pdf
Size:
1.43 MB
Format:
Adobe Portable Document Format
Description:
License bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
2.25 KB
Format:
Item-specific license agreed upon to submission
Description: