Metabolic Cost of Sitting, Standing, and Transitions

February 24, 2015 updated by: Analiza M Silva, PhD, Technical University of Lisbon

What is the Metabolic Cost of Sitting, Standing, and Sit/Stand Transitions? A Randomized Controlled Trial

There is already a lot of scientific evidence supporting the benefits of public health recommendations regarding physical activity (the accumulation of at least 150 minutes of at least moderate intensity physical activity per week). However, these 30 daily minutes represent only about 3% of the waking period. Recent data suggest that most of the population spends on average 8-9 hours / day of sedentary behavior (SB). SB is characterized by any activity with a metabolic cost (MC) below 1.5 METs, mainly actions in the sitting position. In fact, there is evidence that the more time spent sitting higher the risk of disease and mortality, with sitting directly associated with diseases such as type II diabetes, cardiovascular diseases and even cancer. The average life expectancy may increase by ~ 2 years if the investigators reduce sitting about 3h/ day. Additionally, how people accumulate sitting time seems to be a major factor, with prolonged sitting associated with a higher risk of disease. Short-term experimental studies indicate that sedentary lifestyles affect energy balance enhancing weight gain. While there is some research regarding the MC associated with "sitting" and "standing" behaviors, the results are contradictory. Besides these conflicting results, the impact of transitions between these two types of behavior and how these transitions can contribute to MC increase have never been investigated.

Our hypothesis is that, in both men and women, the simple replacement of sitting for "standing" may not substantially increase MC, but instead, the largest contribution may reside on the transitions between these two states of behavior. Therefore, the investigators will perform a study with the following purposes:

Examine MC and HR associated with "sitting", "standing", and transitions between these two types of behavior in adults of both gender, apparently healthy with variable body composition profiles.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Introduction Regular physical activity (PA) positively influences most physiological processes in the human body. Inversely, sedentary behavior (SB)-too much sitting as distinct from too little physical activity-contributes adversely to cardio metabolic health outcomes and premature mortality [1-3]. Obesity results from a long-term excess of energy consumed vs. energy expended, a positive energy balance [4]. While overeating certainly contributes to a positive energy balance, the epidemic of obesity and related metabolic disorders is also driven by reductions in energy expended [5]. Modern human environments are vastly different from those of our ancestors. Technologic developments in transportation, communications, workplaces, and home entertainment confer a wealth of comfort, but increase the time spent in SB which represents costs to human health [6]. With increased use of computers, office workers may remain seated for long periods of time during which metabolic cost (MC) is minimal, making many worksites obesogenic environments [7]. Sitting time not only contributes to positive energy balance but is also an independent risk factor for excess adiposity [8,9] and obesity [10] even among people participating in high levels of moderate-to-vigorous physical activity (MVPA) [11,12]. Even without performing exercise people can have markedly variable low intensity physical activity (LIPA) levels, which in turn substantially varies PA energy expenditure (PAEE) by up to 2000 kcal/day [13]. Emerging evidence supports the feasibility of raising daily MC by replacing office work-related SB with LIPA via workstation alternatives to the traditional office chair and desktop computer-based combinations [14].

Regardless of total sitting time, evidence has been growing on the metabolic benefits of interrupting sitting time more often [15-17], with less focus on MC as a result from these breaks. There is some basic science on the differences of MC associated with "sitting" and "standing", however the results are contradictory [14,18]. Also, other alternatives have been investigated [14,19] and it seems that in terms of MC, sitting on a stability ball or using sit-stand/standing desks are comparable to the traditional seated condition EE (≅1.2 kcal min(-1)). The treadmill and pedal desks (active workstation alternatives) have been shown to offer the greatest promise in terms of EE (≅2-4 kcal min(-1)) [14]. Another strategy is to introduce walking breaks into prolonged sedentary time which according to a recent study [20] can yield an additional 24, 59 or 132 kcal per day, if they stood up and walked at a normal, self-selected pace for one, two or five minutes compared with sitting for the 8-hour working period. From this intervention, heart rate (HR) was also examined to assess differences between conditions with no significant between-condition differences for heart rate. Therefore, taking breaks from sitting is a potential outlet to prevent obesity and the rise of obesity but the real contribution of the simple action of standing up from a seated position and returning to the seated position (sit/stand transition) on MC and HR is yet to be investigated. To overcome these limitations, a randomized controlled trial will be conducted to examine the MC and HR associated with sitting, standing, and transitions between the previous behaviors in laboratory settings and using accurate methods (indirect calorimetry). By including this methodological approach we will be able to estimate the additional contribution of a "break" compared to just standing when accumulating sedentary time on MC and HR [18].

Hypothesis

  1. The percent increase in MC and heart rate (HR) above resting associated with sitting, standing and sitting/stand transitions will be different, independently of gender, body composition, and age.
  2. The MC, either per kg of body weight or per kg of fat-free mass, associated with sitting and standing will be similar but a higher cost is expected for the sitting-to-stand transitions, regardless of gender, age, and FFM.

Purposes

  1. To determine the MC differences between sitting, standing and transitions conditions, adjusting for the effects of gender, body composition, and age.
  2. To determine the HR differences between sitting, standing and transitions, adjusting for the effects of gender, body composition, and age.

Participants Sample power analysis For sample and power calculations we used the (GPower software, version 3.1.9.2) and consider MC as the continuous response variable. Based on a pilot study with a small sample size that aimed to test the differences in MC between the three conditions assessed by indirect calorimetry we have an effect size of approximately 0.385 by using repeated measures ANCOVA. Therefore we will need to study 50 participants to be able to reject the null hypothesis that the population means of the three experimental conditions are equal with probability (power) 0.8. The Type I error probability associated with this test of this null hypothesis is 0.05. Considering a 10% drop out rate may occur due to invalid data we will enroll 60 participants using a crossover design where participants will be randomly assigned to perform the 3 conditions in different orders.

Sample recruitment and selection A total of 60 healthy participants, both men and women will be selected. Participants will be recruited through advertisements placed nearby the institution and volunteer to participate in this study. If inclusion criteria are present participants will be randomly assigned to one of the conditions' orders and participate in the study.

Assessments Anthropometry Subjects will be weighed to the nearest 0.1kg wearing minimal clothes and without shoes and height will be measured to the nearest 0.1cm in a digital scale with integrated stadiometer (Seca, Hamburg, Germany) according to the standardized procedures described elsewhere [21]. BMI will be calculated using the formula [weight(Kg)/height2(m2)].

Body Composition To estimate total fat mass and FFM it will be used the dual energy X-ray absorptiometry (Hologic Explorer-W, Waltham, USA). A whole-body scan will be performed and the attenuation of X-rays pulsed between 70 and 140 kV synchronously with the line frequency for each pixel of the scanned image will be measured.

Resting Energy Expenditure (REE) The REE will be estimated using an open-circuit spirometry system (MedGraphics Corporation, Breezeex Software). Subjects will lye supine for ~45 minutes. The calorimeter device is attached to the mask and breath-by-breath VO2 and VCO2 are measured for a 30 minutes period. Data will be analyzed according to procedures described elsewhere [22].

MC measurement in each testing condition The MC will be estimated using an open-circuit spirometry system (MedGraphics Corporation, Breezeex Software). Each participant will have to complete 4 periods (conditions) of 10 minutes in which the calorimeter device is attached to the mask and breath-by-breath VO2 and VCO2 are measured for 40 minutes. The first condition is to remain seated in a chair, with hands placed on top of the thighs for 10 minutes, remaining motionless. The second condition is identical to the first but the participant is in an upright position (standing). Finally, in the third condition, the participant will perform one sitting-to-stand followed by a stand-to-sitting transition, every minute. The order of the three conditions will be randomly assigned. Heart rate will be measured continuously using a pulse oximeter that is attached to the MedGraphics system. This is a medical device that indirectly monitors the oxygen saturation of a patient's blood (as opposed to measuring oxygen saturation directly through a blood sample). Heart rate and oxygen consumption data will be analyzed minute-by-minute.

Statistical Analysis Statistical analysis will be performed using SPSS Statistics version 22.0, 2013 (SPSS Inc., Chicago, IL). Descriptive statistics (mean ± SD) will be calculated for all outcome measurements. Normality will be verified using the Kolmogorov-Smirnov test. A repeated measure ANCOVA with post hoc analysis will be used to compare the differences between conditions, adjusting for potential covariates (FFM and age) and considering the order of conditions' randomization as a between-subject effect. To test the sphericity or homogeneity of variances, the Mauchly's statistical test will be performed. Statistical significance will be set at (p<0.05)

Risk/benefit analysis The study first aim is to assess the MC associated with sitting, standing, and the sitting-to-stand transitions. By doing this we will be able to estimate the additional contribution of the actual transition to MC comparing to just sitting or standing for longer periods of time. Evidence found SB to have deleterious effects on general health status, specifically associated with a positive energy balance that lead to adiposity and weight gain thus increasing the risk of obesity and related metabolic risk factors. Therefore, participants will only benefit with this intervention [23]. No risk will be added for participating in the study as no risk will be associated with the intervention itself. Recognized and safe techniques will be used to assess MC and body composition.

Privacy and confidentiality of data This research will only take place if approved by the ethics Committee of the Faculdade de Motricidade Humana from Universidade de Lisboa and will be conducted in accordance with the declaration of Helsinki for human studies. All participants will be informed about the possible risks of the investigation before giving their written informed consent to participate. The collected data will be treated and analyzed but confidentiality and privacy will always be kept. Therefore, all the data is collected and treated without any personal identifier and we will never provide the code. The data is kept in excel and SPSS file in the faculty server connected to the Exercise and Health Laboratory. Later the documents received with the data of each participant will be destroyed after the database is constructed.

Participants' compensation and insurance There are no expenses and costs associated with the participation in this study therefore participants will need no insurance. However, as described in the informed consent, transportation to the laboratory will be supported by the participants.

Who to contact in case of emergence? Pedro Júdice.

Conflicts of interest The authors declare that there are no conflicts of interest within this study.

Study Type

Interventional

Enrollment (Actual)

50

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Portugal
    • Lisboa
      • Cruz Quebrada, Lisboa, Portugal, 1495
        • Exercise and Health Laboratory, Faculdade de Motricidade Humana, Universidade de Lisboa

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 64 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Men and women aged 18-64 years and without major metabolic, pulmonary, and cardiac disorders and general health guaranteed.
  • Physically independent and able to perform all the conditions without limitations.

Exclusion Criteria:

  • Pregnancy or engagement in any weight loss program that may affect energy balance.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Sitting
Remain seated in a chair, with hands placed on top of the thighs for 10 minutes, remaining motionless in which the calorimeter device is attached to the mask and breath-by-breath VO2 and VCO2 are measured minute by minute.
Other: Metabolic cost and HR associated with distinct postural behaviors
The order of the three conditions will be randomly assigned and all will be undertaken in laboratory settings. Before engaging in the experimental conditions participants will perform anthropometric and body composition assessments and also the resting EE evaluation. All evaluations will be performed at one time only, starting at 7:00 am in the morning after an overnight fast
Experimental: Standing
Remain in an upright position (standing) with hands placed on the thighs for 10 minutes, remaining motionless in which the calorimeter device is attached to the mask and breath-by-breath VO2 and VCO2 are measured minute by minute.
Other: Metabolic cost and HR associated with distinct postural behaviors
The order of the three conditions will be randomly assigned and all will be undertaken in laboratory settings. Before engaging in the experimental conditions participants will perform anthropometric and body composition assessments and also the resting EE evaluation. All evaluations will be performed at one time only, starting at 7:00 am in the morning after an overnight fast
Experimental: Transitions sit/stand
The participant will perform one sit-to-stand followed by a stand-to-sit transition, every minute in which the calorimeter device is attached to the mask and breath-by-breath VO2 and VCO2 are measured.
Other: Metabolic cost and HR associated with distinct postural behaviors
The order of the three conditions will be randomly assigned and all will be undertaken in laboratory settings. Before engaging in the experimental conditions participants will perform anthropometric and body composition assessments and also the resting EE evaluation. All evaluations will be performed at one time only, starting at 7:00 am in the morning after an overnight fast

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Metabolic cost
Time Frame: 60 minutes (30 from metabolic rest and 30 from conditions)
The MC will be estimated using an open-circuit spirometry system (MedGraphics Corporation, Breezeex Software). Each participant will have to complete 4 periods (conditions) of 10 minutes in which the calorimeter device is attached to the mask and breath-by-breath VO2 and VCO2 are measured for 40 minutes.
60 minutes (30 from metabolic rest and 30 from conditions)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Heart rate
Time Frame: 60 minutes (30 from metabolic rest and 30 from conditions)
Heart rate will be measured continuously using a pulse oximeter that is attached to the MedGraphics system. This is a medical device that indirectly monitors the oxygen saturation of a patient's blood (as opposed to measuring oxygen saturation directly through a blood sample). Heart rate and oxygen consumption data will be analyzed minute-by-minute.
60 minutes (30 from metabolic rest and 30 from conditions)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Technical University of Lisbon

Investigators

  • Principal Investigator: Analiza M Silva, PhD, Laboratory of Exercise and Health, Faculadde Motricidade Humana, Universidade de Lisboa

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2014

Primary Completion (Actual)

February 1, 2015

Study Completion (Actual)

February 1, 2015

Study Registration Dates

First Submitted

February 18, 2015

First Submitted That Met QC Criteria

February 24, 2015

First Posted (Estimate)

March 3, 2015

Study Record Updates

Last Update Posted (Estimate)

March 3, 2015

Last Update Submitted That Met QC Criteria

February 24, 2015

Last Verified

February 1, 2015

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • Transitions study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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