Hypertension and related diseases Circulatory System Essential (primary) hypertension
Conditions
Interventions
Five family physician offices mailed invitations to their patients aged 65 years and older to participate in the trial. Eligible and consenting adults are randomly allocated to one of two blood pressu
Sponsors
Bruyere Research Institute (Canada)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Community dwelling adults aged 65 years and older registered with five family physicians
Exclusion criteria
Exclusion criteria: Patients in hospital or living in long-term care facilities.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| After trial participants attended the first session to have their blood pressure measured, they were asked to come to the next two visits with less than a week between visits. The mean time interval to complete the three BP measurements for Arm A versus Arm B did not significantly differ (Arm A = 11.1 days versus Arm B = 11.8 days (p=0.36)). | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcome measures | — |
Countries
Canada
Outcome results
None listed