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Clinical Trials/NCT05425797
NCT05425797
Completed
Not Applicable

Building on Existing Tools To Improve Chronic Disease Prevention and Screening in Primary Care Virtually: the Virtual BETTER Study

Memorial University of Newfoundland1 site in 1 country92 target enrollmentMarch 31, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Delivery Modality of BETTER Intervention
Sponsor
Memorial University of Newfoundland
Enrollment
92
Locations
1
Primary Endpoint
Readiness to Change (University of Rhode Island Change Assessment Scale: URICA)
Status
Completed
Last Updated
last year

Overview

Brief Summary

The focus of this project is to examine how delivering virtual care impacts health behaviour change for patients with chronic illnesses compared to in-person visits using a chronic disease prevention and screening (CDPS) program called BETTER (Building on Existing Tools To ImprovE Chronic Disease PRevention and Screening in Primary Care).

Detailed Description

While the current pandemic has launched a likely irreversible transition towards increased utilization of virtual methods for delivery of healthcare, we have only a very superficial understanding of how this shift will affect health outcomes and equity of access to health services. Several randomized trials comparing virtual to in-person delivery of health services have been completed, but none have examined the effect of interventions to address health behaviours, arguably one of the most challenging issues in healthcare and one that is most sensitive to the therapeutic relationship and modifiers to that relationship such as the mode of communication. The focus of this project is to examine how delivering virtual care impacts health behaviour change for patients with chronic illnesses compared to in-person visits using a chronic disease prevention and screening (CDPS) program called BETTER (Building on Existing Tools To ImprovE Chronic Disease PRevention and Screening in Primary Care).

Registry
clinicaltrials.gov
Start Date
March 31, 2023
End Date
August 30, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kris Aubrey-Bassler

Associate Professor

Memorial University of Newfoundland

Eligibility Criteria

Inclusion Criteria

  • Persons aged 40-70
  • Persons who are already booking a BETTER prevention visit.

Exclusion Criteria

  • Persons with the presence of a terminal illness
  • Persons in active treatment (i.e., systemic and/or radiation therapy) for cancer.
  • Persons who are unable to provide informed consent.

Outcomes

Primary Outcomes

Readiness to Change (University of Rhode Island Change Assessment Scale: URICA)

Time Frame: Post-Visit (less than 1 week after visit)

To compare readiness to implement lifestyle change after telephone, video, and in-person BETTER Prevention visits. Min Score: 4 Max Score: 20 Higher scores indicate a higher readiness to change (better outcome)

Secondary Outcomes

  • Satisfaction of Modalities (Client Satisfaction Questionnaire: CSQ-4)(Post-Visit (less than 1 week after visit))
  • Acceptability(Enrollment (Pre-visit))
  • Accessibility(Enrollment (Pre-visit))

Study Sites (1)

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