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The Virtual BETTER Study

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05425797
Enrollment
92
Registered
2022-06-21
Start date
2023-03-31
Completion date
2024-08-30
Last updated
2024-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delivery Modality of BETTER Intervention

Keywords

chronic disease, lifestyle, screening, physical activity, diet

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).

Interventions

OTHERIn-Person Prevention Practitioner Visit

BETTER Intervention visit with PP which will take place in-person at the PP's office.

OTHERVideo-Call Prevention Practitioner Visit

BETTER Intervention visit with PP which will take place virtually via a secure video system.

OTHERPhone Prevention Practitioner Visit

BETTER Intervention visit with PP which will take place via telephone.

Sponsors

Memorial University of Newfoundland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Investigator)

Intervention model description

We will study two experimental groups (telephone and video) compared to the control group of in-person BETTER intervention delivery. Mode of delivery will be randomized between patients. If it is not feasible yo offer all three (e.g. PP only has capacity to offer virtual appointments, study population lives greater than 30 minutes travel from PP location), a subset of the three will be offered.

Eligibility

Sex/Gender
ALL
Age
40 Years to 70 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

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

MeasureTime frameDescription
Satisfaction of Modalities (Client Satisfaction Questionnaire: CSQ-4)Post-Visit (less than 1 week after visit)To assess satisfaction with the three different delivery modalities. Min Score: 4 Max Score: 16 Higher scores indicate higher satisfaction (better outcome)
AcceptabilityEnrollment (Pre-visit)To assess acceptability of the three different delivery modalities. Assessed through enrollment questionnaire which will ask which delivery method they agree to. (Not scored on scale)
AccessibilityEnrollment (Pre-visit)To assess accessibility of the three different delivery modalities. Assessed through enrollment questionnaire which will ask why they chose which delivery method they did. (Not scored on scale)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026