Stand Up for Your Health: The Up Project

NCT ID: NCT05844267

Last Updated: 2024-01-03

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-03-20
• Study Completion Date: 2023-09-30

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.

Detailed Description

The design of The Up Project will be a Quasi-experimental controlled trial controlled trial in which participants will undergo two interventions aimed at reducing sedentary behavior in the workplace. The sample size was calculated using G*Power software and will consist of 60 workers from three higher education centers located in the Valparaiso region of Chile. Participants will be divided into three groups: a) a control group, b) a group with booster breaks led by professionals, and c) a group with computer prompts that are unled.

The study will be conducted in three stages, comprising two visits to our laboratory and one visit to the participants' offices. The first stage will involve a pre-intervention measurement session at our laboratory, which will comprehensively assess various cardiometabolic risk factors, such as body composition (DXA), waist circumference, weight, height, resting heart rate, and blood pressure. Questionnaires will also be administered to assess stress perception (PSS-14), occupational pain (using the Nordic-standardized questionnaire), physical activity (GPAQ), sedentary time at work (OSPAQ), 24-hour behavior (DABQ), eating habits (using the Mediterranean diet adherence questionnaire), smoking habits (using the Fargerstörm test), and socio-economic status (using the distribution and average autonomous income of households by income decile). Furthermore, participants will wear two types of accelerometers, ActiGraph and ActivPAL, for seven days to objectively measure physical activity intensity, sedentary time, and sedentary time breaks.

In the second stage, our research team will visit the participants' offices to remove the devices and administer the questionnaire application for sedentary time at work and 24-hour behavior for a second time. The intervention will commence after the accelerometers have been removed.

Finally, the third stage will involve a second visit to our laboratory, where cardiometabolic risk will be re-evaluated, and questionnaires on stress perception, occupational pain, physical activity, sedentary time at work, and 24-hour behavior will be administered again.

It is worth highlighting that mid-intervention, all three groups will be provided with accelerometers to re-evaluate the subjects' daily physical activity intensity, sedentary time, and breaks in sedentary time.

Intervention

The intervention will be conducted from Monday to Friday over a period of 12 weeks. The "Booster Breaks group" will receive a visit from a physical education teacher who will guide them through exercises based on the Chilean safety association (ACHS) guidelines. These exercises will last for an average of 14-16 minutes per day, and will be of light to moderate intensity, consistent with the intensity levels established during our pilot study.

The "Computer Prompts group" will have an offline messaging application ("Ponte de Pie por tu Salud") installed on their computers. The application will generate a message each hour, inviting the participants to stand up and perform exercises for 2 minutes. This will accumulate to an average of 14-16 minutes of active breaks daily. We will also be able to collect data on whether the participant rejected the break or proposed an alternative time.

It is important to note that both interventions will be equivalent in terms of intensity and time. The exercises for the "Booster Breaks group" will be performed at the same intensity and for the same duration (14-16 minutes) as the "Computer Prompts group." A detailed exercise plan for both groups can be found in the supplementary material.

The control group will only be evaluated pre and post-intervention and will be advised to continue with their usual routine.

Measurement of cardiometabolic risk factors:

Weight and Height: Weight was measured with a digital balance in which precision and maximum weight were of 0.1 and 150 kg respectively (OMROM. HN-289-LA). Height with a portable stadiometer (SECA, model 213, GmbH).

Body composition: Fat mass, fat-free mass, and bone mass will be assessed using a dual X-ray absorptiometer (General Electrics, model Lunar, series 212069). Both the equipment, box, and evaluators have been approved by the Health Service of the Region of Valparaiso.

Waist circumference: the minimum waist will be measured with a Lufkin metallic tape measure (W606PM) after exhaling.

Blood pressure: will be measured on the left arm with a digital monitor model HEM-7120 (OMRON, Illinois, USA) which provides both diastolic and systolic blood pressure values. It will be evaluated twice after 5 min of rest and the values will be averaged.

Resting heart rate: After the resting blood pressure assessment the minimum heart rate value will be recorded with a pulse oximeter model Prince-100B5 (Heal Force).

Measurement of physical activity and sedentary behavior:

Accelerometry: Time spent in sedentary and physical activity (and their intensities) will be objectively assessed with two accelerometers: the ActiGraph (Model GT3X+, Actigraph, Illinois, USA) and the ActivPAL ™ . Participants will use both devices for 7 consecutive days. The ActiGraph will be worn on the wrist, like a watch, which does not inconvenience one's routine tasks. It should only be removed for water activities (swimming) and showering. The ActivePAL is water-resistant and will be attached to the front of the right thigh with a hypoallergenic strap. Participants will also keep a monitoring diary to record how many times they used the accelerometers each day, the days they worked and the times they started and finished work on each of those days. Sleep quality will also be assessed with the GT3X+.

Self-reporting of physical activity: Global Physical Activity Questionnaire (GPAQ) is a questionnaire used by the World Health Organization to monitor physical activity levels worldwide (Bull et al., 2009).

Self-reporting of sedentary time at work: Occupational Sitting and Physical Activity Questionnaire (OSPAQ), allows the identification of the percentages of time the subject spends sitting down during the working day in which he/she works (Chau et al., 2012).

Self-reporting of behavior within 24 hours: Daily Activities Behavior Questionnaire (DABQ) allows the identification of the subject's behavior in terms of physical activity, sedentary time, and sleep in 24 hours (Kastelic et al., 2022).

Measurement of Stress Perceived Stress Scale Questionnaire (PSS-14): The questionnaire was originally developed and validated by Cohen, Kamarck, and Mermelstein in 1983. It has been adapted for use with Chilean adults and allows for the determination of an individual's stress level by scoring various domains related to stress tolerance using a Likert scale.

Measurement of Occupational Pain The Nordic standardized questionnaire will be used to assess the participants' perception of musculoskeletal symptoms related to their work. This questionnaire is a well-established tool for identifying and evaluating musculoskeletal problems and will allow us to gather information on any discomfort or pain experienced by the participants in their working environment. The questionnaire is designed to focus on the body areas most commonly affected by work-related musculoskeletal disorders, such as the neck, shoulders, back, and wrists. By using this questionnaire, we can identify any specific areas where participants may be experiencing pain or discomfort and tailor our intervention to address these issues (Kuorinka et al., 1987).

Measurement of Eating Habits Mediterranean diet adherence questionnaire. The questionnaire will be used to measure the subjects' adherence to the Mediterranean diet to determine its relationship with cardiometabolic factors (Martínez-González et al., 2012).

Measurement of smoking habits Fargerstörm test is a questionnaire that scores with a liker scale different aspects of smoking habits, which allows to determine the level of dependence to this substance (Heatherton et al., 1991).

Measurement of Socio-economic Status Distribution and average autonomous income of households by income decile. This questionnaire will be used to obtain the per capita income of the participants in order to have data on the socio-economic level of the subject. This questionnaire is made under the guidelines of the "Asesoria Tecnica Parlamentaria" of the Chilean government.

Conditions

Sedentary Behavior

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: SINGLE

Study Groups

Booster Breaks group (led breaks)

Participants 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.

Group Type: EXPERIMENTAL

Experimental led booster breaks

Intervention Type: BEHAVIORAL

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.

Computer Prompts group (unled breaks)

Active 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.

Group Type: EXPERIMENTAL

Experimental unled computer-prompts

Intervention Type: BEHAVIORAL

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.

Control

The group will participate in evaluations pre-post but not interventions. We will recommend continuing with their usual routine.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Experimental led booster breaks

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.

Intervention Type: BEHAVIORAL

Experimental unled computer-prompts

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.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Office workers who are physically and mentally healthy and work for 44 hours a week.

Exclusion Criteria

• 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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Pontificia Universidad Catolica de Valparaiso

OTHER

Sponsor Role: lead

Responsible Party

Carlos Cristi Montero

Professor, School of Physical Education, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Carlos Cristi-Montero, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Pontificia Universidad Católica de Valparaiso, Valparaiso,Chile

Locations

School of Physical Education, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile

Valparaíso, Región de Valparaíso, Chile

Countries

Chile

Other Identifiers

BIOPUCV-HB 580-2023

Identifier Type: -

Identifier Source: org_study_id