I10.90
Conditions
Interventions
Group 1: Sixty-five young and healthy adults were eligible for inclusion if they were without cardiovascular disease, were not obese, and did not present conditions that could interfere with standardi
cuff size CA04: 22–42 cm) and Welch Allyn ProBP 2000 (Welch Allyn Inc., Skaneateles Falls, NY, USA, cuff size [43]). Device order was randomized apriori to minimize potential order effects. A randomiz
Sponsors
Leuphana Universität Lüneburg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Participants were eligible for inclusion if they were without cardiovascular disease, were not obese, and did not present conditions that could interfere with standardized blood pressure measurement procedures.
Exclusion criteria
Exclusion criteria: Participants were ineligible for inclusion if they had cardiovascular disease, were obese, or had conditions that could interfere with standardized blood pressure measurements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Systolic and diastolic blood pressure were defined as the primary outcome variables. They are recorded using the respective measuring devices under various conditions during the five blood pressure measurements taken at each appointment and are compared with one another in the data analysis. | — |
Secondary
| Measure | Time frame |
|---|---|
| Heart rate, as provided by the oscillometric devices, was recorded as a secondary outcome to evaluate whether reliability patterns observed for blood pressure were also evident for another physiological parameter. They are recorded simultaneously with systolic and diastolic blood pressure during the five blood pressure measurements taken per appointment using the respective devices under various conditions, and are compared with one another in the data analysis. | — |
Countries
Germany
Contacts
Public ContactKonstantin Warneke
Leuphana Universität Lüneburg
Outcome results
None listed