Cardiovascular Diseases Clinical Trial
— WALKOfficial title:
The Role of a Motion Sensor With Accompanying Web Application on Step Counts, Energy Balance, and Metabolic Markers in Nurses
Verified date | September 2023 |
Source | Ottawa Heart Institute Research Corporation |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this prospective randomized controlled trial is to explore the role of a motion sensor with accompany web application on step counts, energy balance, and metabolic markers in nurses. Additionally, eating behaviours, behavioural regulation in exercise, and mood states that may impact these parameters will also be examined.
Status | Completed |
Enrollment | 76 |
Est. completion date | August 1, 2015 |
Est. primary completion date | April 25, 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 90 Years |
Eligibility | Inclusion Criteria: - 1. Participant must be a registered nurse with the University of Ottawa Heart Institute; 2. Participant must be 18 years of age or older; 3. Participant must be able to walk unassisted; 4. Participant is able and willing to provide informed consent. Exclusion Criteria: 1. Participant is pregnant, lactating or planning to become pregnant during the study period; 2. Participant is unable to read and understand English; 3. Medical contraindications to exercise; 4. Already using a motion sensor device to track physical activity. - |
Country | Name | City | State |
---|---|---|---|
Canada | University of Ottawa Heart Institute | Ottawa | Ontario |
Lead Sponsor | Collaborator |
---|---|
Ottawa Heart Institute Research Corporation |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Step counts | All participants will be asked to wear a Tractivity® motion sensor device on their ankle for to assess their daily step count and physical activity energy expenditure | 6 weeks during observation and 6 weeks during intervention | |
Secondary | Body Mass (kg) | Body weight will be measured using a digital scale to the nearest 0.1 kilogram | Screening (week 1), Observation (weeks 2-5), during the intervention (weeks 6-9), post study at week 26 and week 52 | |
Secondary | Waist Circumference | Waist circumference will be measured using a tape measure | Screening (week 1), Observation (weeks 2-5), during the intervention (weeks 6-9), post study at week 26 and week 52 | |
Secondary | Fat mass | Fat mass will be measured using bioelectrical impedance analysis | Screening (week 1), Observation (weeks 2-5), during the intervention (weeks 6-9), post study at week 26 and week 52 |
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