- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03137836
Classroom Standing Desks for Reducing Sitting Time in Children
Effects of Sit-to-stand Desks on Behavior and Cognitive Function in Children
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Lisbon, Portugal, 1800-071
- Danilo Rodrigues Pereira da Silva
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Aged between 11 and 13 years-old
- Be able to postural changes
Exclusion Criteria:
- Do not return the written informed consent properly signed by parents/guardians
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention
Sit-to-stand desks (Ergotron LearnFit®) will replace standard desks.
In addition, meeting with parents and teacher's training will be conducted in order to support behavior change.
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Multi-level intervention focused on school environment (furniture) will be conducted. Device: Sit-to-stand desks (Ergotron LearnFit®); Device: (Actigraph, Pensacola, FL, USA); Device: ActivPALTM . |
No Intervention: Control
Control classroom will maintain their routine in sitting desks.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Sedentary behavior
Time Frame: 16 weeks
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Sedentary behavior will be assessed trough the sitting time (min/day) given by ActivPALTM micro device (PAL Technologies Limited, Glasgow, UK).
The device will be attached on anterior mid-line of the participants right thigh though 3MTM TegadermTM Transparent Film Roll (4 in x 11yd).
Participants will wear the inclinometer continuously for seven days, including shower and sleep time, except in swimming activities.
The ActivPAL3TM software v.7.2.32 will be used to data reduction.
In addition to the baseline and follow-up measurements, the inclinometer will be used during the intervention just in school time to better clarify the sit-to-stand desks use.
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16 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Physical activity
Time Frame: 16 weeks
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Physical activity will be measured though Actigraph GT3X+ accelerometers (Actigraph, Pensacola, FL, USA).
Participants will be instructed to wear the device on the right rip (near the iliac crest) during waking hours for seven days.
The device will be attached via an elastic belt and must will removed only in water-based activities.
Will be considered a valid evaluations which had four or more days (including one of weekend) of a minimum of 600 minutes of wear.
The Choi et al. [16] criteria of wear time and Evenson et al. [17] cuttoffs to PA intensities will be applicable with 15s epochs (collected at 30Hz) by Actilife v.6.10.4.
The participants shall register in daily record the time which the device is removed and the reason.
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16 weeks
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Academic achievement
Time Frame: 16 weeks
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Participants grades will be obtained in both assessments points.
Individual and sum of disciplines grades changes will be considered to comparisons purposes.
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16 weeks
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Participants self-reported measurements
Time Frame: 16 weeks
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Information about self-perception of physical and mental health, academic performance, behaviors (exercise and sleep habits) and social relationship will be assessed by a specific questionnaire for the participants.
In addition, the intervention group ones will report their expectations (before) and perceptions (after) of the standing desks use.
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16 weeks
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Stakeholders perceptions
Time Frame: 16 weeks
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Parents/guardians (individual level) and teachers perceptions (cluster level) about discipline, social interaction, academic performance and health behaviors of the children will be collected by a questionnaire filled before and after the intervention.
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16 weeks
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Cost-effectiveness
Time Frame: 16 weeks
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Considering the costs of classroom environmental adaptations and their effects on primary and secondary outcomes, the incremental cost-effectiveness ratio will be calculated comparing with costs of a traditional classroom.
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16 weeks
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Cognitive function - Coop Corsi block-tapping test
Time Frame: 16 weeks
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Visual-spatial working memory capacity will be assessed through Coop Corsi block-tapping test.
A 3 × 3 grid of 9 blocks indicates a spatial sequence by changing the colour of one block at a time, and participants were then asked to repeat that sequence by clicking on the blocks in the same order.
During the 12 trials, sequence length increased by 1 block location each time the participant correctly repeated the sequence.
Any error in repeating a sequence led to the next sequence being shortened by one location.
The variable of interest was mean memory span, calculated as the average length of the three longest correctly repeated sequences.
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16 weeks
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Cognitive function - Stroop color test
Time Frame: 16 weeks
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Sensitivity to interference and the ability to suppress an automated response will be assessed using the Stroop color test.
The Stroop test consists in two levels.
Both levels involve the test word being placed in the center of the screen, with the target and distractor presented randomly on the right or left of the test word.
The target position was counterbalanced for the left and right side within each test level.
The participant is asked to respond as quickly as possible, using the left and right arrow keys, to identify the position of the target word.
The variable of interest is the proportion of correct responses made.
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16 weeks
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Cognitive function - d2 test
Time Frame: 16 weeks
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Sustained attention and visual scanning ability will be assessed using the d2 test. This paper-and-pencil task requires participants to detect "d" symbols with two dashes (that may be located either both above, both below, or one above and one below the "d") among distractors ("d's" with one, three, or four marks or "p's" with one or two marks). The concentration performance score was determined on the number of correct responses minus errors. Higher scores indicate a better and more stable performance. |
16 weeks
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Neuropsychological assessment - Raven's matrices test
Time Frame: 16 weeks
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Neuropsychological assessment will be assessed using the Raven's Progressive Matrices.
The test provides a simplified 36-item paper format.
Each item contains a pattern problem with one part removed and six pictured inserts of which one contains the correct pattern.
Participants point to the pattern piece they select or to its number.
The total score is the total number of matrices completed correctly, and the test is thus scored out of 36.
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16 weeks
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Neuropsychological assessment - Rey-Osterrieth complex figure test
Time Frame: 16 weeks
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Neuropsychological assessment will be assessed using the Rey-Osterrieth complex figure test.
The Rey-Osterrieth complex figure test (ROCF) is a neuropsychological assessment in which participants are asked to reproduce a complicated line drawing, first by copying it freehand (direct), and then drawing from memory (delayed copying).
ROCF includes 18 units and the maximum score for each of the two tasks (direct and delayed copying) is 36.
Two points are given when the element is correctly reproduced, 1 point when the reproduction is distorted, incomplete but placed properly, or complete but placed poorly; 0.5 point is credited when the element is distorted or incomplete and placed poorly.
A zero score is given when the unit is absent or not recognizable.
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16 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Luís Sardinha, PhD, University of Lisbon
Publications and helpful links
General Publications
- Choi L, Liu Z, Matthews CE, Buchowski MS. Validation of accelerometer wear and nonwear time classification algorithm. Med Sci Sports Exerc. 2011 Feb;43(2):357-64. doi: 10.1249/MSS.0b013e3181ed61a3.
- Biswas A, Oh PI, Faulkner GE, Bajaj RR, Silver MA, Mitchell MS, Alter DA. Sedentary time and its association with risk for disease incidence, mortality, and hospitalization in adults: a systematic review and meta-analysis. Ann Intern Med. 2015 Jan 20;162(2):123-32. doi: 10.7326/M14-1651. Erratum In: Ann Intern Med. 2015 Sep 1;163(5):400.
- Benden ME, Blake JJ, Wendel ML, Huber JC Jr. The impact of stand-biased desks in classrooms on calorie expenditure in children. Am J Public Health. 2011 Aug;101(8):1433-6. doi: 10.2105/AJPH.2010.300072. Epub 2011 Mar 18.
- Gardner B, Smith L, Lorencatto F, Hamer M, Biddle SJ. How to reduce sitting time? A review of behaviour change strategies used in sedentary behaviour reduction interventions among adults. Health Psychol Rev. 2016;10(1):89-112. doi: 10.1080/17437199.2015.1082146. Epub 2015 Sep 16.
- Owen N. Sedentary behavior: understanding and influencing adults' prolonged sitting time. Prev Med. 2012 Dec;55(6):535-9. doi: 10.1016/j.ypmed.2012.08.024. Epub 2012 Sep 8.
- Evenson KR, Catellier DJ, Gill K, Ondrak KS, McMurray RG. Calibration of two objective measures of physical activity for children. J Sports Sci. 2008 Dec;26(14):1557-65. doi: 10.1080/02640410802334196.
- Owen N, Sugiyama T, Eakin EE, Gardiner PA, Tremblay MS, Sallis JF. Adults' sedentary behavior determinants and interventions. Am J Prev Med. 2011 Aug;41(2):189-96. doi: 10.1016/j.amepre.2011.05.013.
- Prince SA, Saunders TJ, Gresty K, Reid RD. A comparison of the effectiveness of physical activity and sedentary behaviour interventions in reducing sedentary time in adults: a systematic review and meta-analysis of controlled trials. Obes Rev. 2014 Nov;15(11):905-19. doi: 10.1111/obr.12215. Epub 2014 Aug 11.
- Sedentary Behaviour Research Network. Letter to the editor: standardized use of the terms "sedentary" and "sedentary behaviours". Appl Physiol Nutr Metab. 2012 Jun;37(3):540-2. doi: 10.1139/h2012-024. Epub 2012 Apr 27. No abstract available.
- Tremblay MS, LeBlanc AG, Kho ME, Saunders TJ, Larouche R, Colley RC, Goldfield G, Connor Gorber S. Systematic review of sedentary behaviour and health indicators in school-aged children and youth. Int J Behav Nutr Phys Act. 2011 Sep 21;8:98. doi: 10.1186/1479-5868-8-98.
- Ridgers ND, Salmon J, Ridley K, O'Connell E, Arundell L, Timperio A. Agreement between activPAL and ActiGraph for assessing children's sedentary time. Int J Behav Nutr Phys Act. 2012 Feb 19;9:15. doi: 10.1186/1479-5868-9-15.
- Clemes SA, Barber SE, Bingham DD, Ridgers ND, Fletcher E, Pearson N, Salmon J, Dunstan DW. Reducing children's classroom sitting time using sit-to-stand desks: findings from pilot studies in UK and Australian primary schools. J Public Health (Oxf). 2016 Sep;38(3):526-533. doi: 10.1093/pubmed/fdv084. Epub 2015 Jun 14.
- Hinckson E, Salmon J, Benden M, Clemes SA, Sudholz B, Barber SE, Aminian S, Ridgers ND. Standing Classrooms: Research and Lessons Learned from Around the World. Sports Med. 2016 Jul;46(7):977-87. doi: 10.1007/s40279-015-0436-2. Erratum In: Sports Med. 2016 Feb;46(2):297.
- Minges KE, Chao AM, Irwin ML, Owen N, Park C, Whittemore R, Salmon J. Classroom Standing Desks and Sedentary Behavior: A Systematic Review. Pediatrics. 2016 Feb;137(2):e20153087. doi: 10.1542/peds.2015-3087. Epub 2016 Jan 22.
- Mirwald RL, Baxter-Jones AD, Bailey DA, Beunen GP. An assessment of maturity from anthropometric measurements. Med Sci Sports Exerc. 2002 Apr;34(4):689-94. doi: 10.1097/00005768-200204000-00020.
- Silva DR, Machado DGS, Pinto F, Judice PB, Minderico CS, Collings PJ, Cyrino ES, Sardinha LB. Effect of a 16-week multi-level classroom standing desk intervention on cognitive performance and academic achievement in adolescents. Sci Rep. 2022 Sep 1;12(1):14504. doi: 10.1038/s41598-022-18248-y.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- LSardinha
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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