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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04524572
Other study ID # 20130429
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 26, 2013
Est. completion date August 1, 2015

Study information

Verified date September 2023
Source Ottawa Heart Institute Research Corporation
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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. -

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Motion sensor
To explore the role of a motion sensor with accompanying web application on step counts, energy balance, and metabolic markers in nurses

Locations

Country Name City State
Canada University of Ottawa Heart Institute Ottawa Ontario

Sponsors (1)

Lead Sponsor Collaborator
Ottawa Heart Institute Research Corporation

Country where clinical trial is conducted

Canada, 

Outcome

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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