Stand Up for Your Health: The Up Project
TUP
Sedentary Behavior With Physical Activity Breaks Aimed at Improving Cardiometabolic Risk Factors in Workers
1 other identifier
interventional
60
1 country
1
Brief Summary
In today's modern workplace, desk-based work is prevalent, leading to prolonged periods of sitting and limited physical activity among workers. This sedentary behavior can have detrimental effects on the physical and mental health of employees. Besides, this behavior contributes to the rising incidence of metabolic and general health problems in workers, even independently of their physical activity levels, leading to reduced productivity for the company and an increased economic burden on public health. The Up Project is a Quasi-experimental controlled trial designed to assess the efficacy of two interventions to reduce sedentary behavior in the workplace. The study involves three groups: a) a control group, b) a group with booster breaks (led by professionals), and c) a group with unled computer prompts. The primary outcomes being measured are cardiometabolic risk and stress perception, while secondary outcomes include physical activity, sedentary behavior, and occupational pain. This study is expected to contribute to the research gap in this area by providing valuable insights into the efficacy of interventions aimed at reducing sedentary behavior and its impact on health in the workplace.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 20, 2023
CompletedFirst Submitted
Initial submission to the registry
April 24, 2023
CompletedFirst Posted
Study publicly available on registry
May 6, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2023
CompletedJanuary 3, 2024
December 1, 2023
6 months
April 24, 2023
December 30, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Cardiometabolic Risk
Measurements related to cardiometabolic risk will be obtained through various methods, including DXA scans (General Electrics, model Lunar, series 212069) to determine body composition such as fat mass, fat-free mass, and bone mass. Weight will be measured in kilograms using a digital balance (OMRON HN-289-LA), height will be taken in centimeters with a portable stadiometer (SECA, model 213, GmbH). Additionally, weight and height will be combined to report BMI in kg/m\^2. Waist circumference will be measured in centimeters using a Lufkin metallic tape measure (W606PM), while blood pressure will be measured in millimeters of mercury (mm Hg) using a digital monitor (model HEM-7120, OMRON) and heart rate will be measured in beats per minute using a pulse oximeter model Prince-100B5 (Heal Force).
up to six months
Stress Perception
To measure stress perception, we will use the Perceived Stress Scale Questionnaire (PSS-14), which was validated by Cohen, Kamarck, and Mermelstein in 1983 and adapted for Chile by Erik Marín (Marín et al., 2004). The questionnaire assesses the individual's perception of various situations that may be influenced by their level of stress. The PSS-14 questions refer to the last month and are rated on a Likert scale ranging from 0 (never) to 4 (very often) in which a higher score indicates a higher level of perceived stress.
up to six months
Secondary Outcomes (2)
Occupational pain
up to six months
Physical Activity and Sedentary Time
up to six months
Study Arms (3)
Booster Breaks group (led breaks)
EXPERIMENTALParticipants will engage in active breaks led by a professional, where they will perform various exercises based on the guidelines provided by the Chilean safety association (ACHS). These breaks will have an average duration of 14-16 minutes per day and will take place from Monday to Friday for a period of 12 weeks.
Computer Prompts group (unled breaks)
EXPERIMENTALActive breaks will be guided by an application called "Ponte de Pie por tu Salud," designed by the Chilean Ministry of Health which will be installed on the participants' computers. The application will be configured to generate breaks every hour for a duration of 2 minutes for 8 hours, ensuring that an average of 14-16 minutes of active breaks are accumulated throughout the day.
Control
NO INTERVENTIONThe group will participate in evaluations pre-post but not interventions. We will recommend continuing with their usual routine.
Interventions
Participants in this group will receive interventions in the form of active breaks, administered by professionals in the relevant field, such as Physical Education teachers, for a period of 12 weeks. The active breaks will comprise exercises of light-to-moderate intensity, based on the guidelines provided by the Chilean safety association (ACHS), with an average duration of 14-16 minutes per day from Monday to Friday. The exercise types and progression will be elaborated in our protocol and published as supplementary material.
Participants in this group will receive interventions in the form of active breaks, facilitated through an application called "Ponte de pie por tu salud," proposed by the Chilean Ministry of Health. This off-line application will be configured to generate breaks every hour, lasting for 2 minutes per break, over the course of 8 hours. This ensures that an average of 14-16 minutes of active breaks are accumulated throughout the day. Our research team will install the application on the participants' work computers and collect data from these computers weekly. At the end of the intervention period, the application will be uninstalled if necessary.
Eligibility Criteria
You may qualify if:
- Office workers who are physically and mentally healthy and work for 44 hours a week.
You may not qualify if:
- Individuals with physical limitations for physical exercise or undergoing weight loss treatment, pregnant women, or pacemaker users will be excluded.
- Participants who have another full-time job or part-time work in another job will also be excluded.
- Data from participants with a participation frequency of less than 70% in the physical activity sessions will not be considered.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
School of Physical Education, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile
Valparaíso, Región de Valparaíso, Chile
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Carlos Cristi-Montero, Ph.D.
Pontificia Universidad Católica de Valparaiso, Valparaiso,Chile
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- SINGLE
- Who Masked
- INVESTIGATOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor, School of Physical Education, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile
Study Record Dates
First Submitted
April 24, 2023
First Posted
May 6, 2023
Study Start
March 20, 2023
Primary Completion
September 30, 2023
Study Completion
September 30, 2023
Last Updated
January 3, 2024
Record last verified: 2023-12