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Workplace Intervention to Reduce Sitting Time: a Randomized Clinical Trial.

U

Universidad del Desarrollo

Status

Completed

Conditions

Office Workers
Sedentary Behavior

Treatments

Behavioral: Computer prompt "Stand up for your Health®"

Study type

Interventional

Funder types

Other

Identifiers

NCT05790837
280-2022

Details and patient eligibility

About

The goal of this randomized clinical trial is to determine the effect of the computer prompt to break sitting time in office workers.

The main question is: What is the effect of the computer prompt "Stand Up for Your Health®" plus education on sitting time, musculoskeletal symptoms, cardiometabolic markers, and physical activity in office workers compared with only education? In addition, to determine the level of adherence to the intervention program by identifying barriers and facilitators referred by the participants.

The participants will be divided into two groups, the experimental and the control group. The participants in the experimental group will use the computer prompt on their desktop and receive information about sedentary behaviour, and the control group will receive only information. All participants will wear accelerometers for one week. The musculoskeletal symptoms and cardiometabolic markers will be measured at baseline, 3rd and 6th month.

Full description

Sedentary behaviour and physical inactivity are risk factors for noncommunicable diseases related to the work environment. The accumulation of sitting time during the workday is related to musculoskeletal symptoms and worse cardiometabolic indicators.

The purpose of this study is to determine the effect of the "Stand up for your Health®" computer app on sitting time, musculoskeletal symptoms, cardiometabolic markers, and physical activity in office workers. Also, to determine the adherence to the intervention program by identifying barriers and facilitators referred by the participants.

In this 2-arm randomized controlled trial, both groups will be recruited from educational establishments and will be measured at baseline, 3rd, and 6th months. The experimental group will be implementing the "Stand Up for Your Health®" computer app plus educational information, while the control group will only receive educational information.

The same measurements will be completed in both groups during a 6 months follow-up period: sedentary behaviour using the Actigraph accelerometers and the Occupational Sitting and Physical Activity Questionnaire (OSPAQ); musculoskeletal symptoms will be assessed by a pressure pain algometer and the Standardized Nordic Questionnaire of Perception of musculoskeletal Symptoms; and cardiometabolic markers and anthropometric measurements will also be assessed according to protocol.

Enrollment

106 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • office workers over 18 years of age,
  • Full-time employees (≥35 hours per week);
  • Spend most of their workday sitting (> 60%). This will be initially self-reported and used as selection criteria prior to the initial consent and measurement visit. This will be later confirmed using accelerometers;
  • Work in the same office place during the week; and
  • Able to walk without using an assistive device or requiring the assistance of another person.

Exclusion criteria

  • Pregnant women;
  • Desktop workers using a height-adjustable workstation; and
  • Office workers sufficiently active according to WHO criteria.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

106 participants in 2 patient groups

Computer prompt + Education (CP+E)
Experimental group
Description:
The intervention group consists of the implementation of the desktop application "Stand up for your Health®" following the model proposed by the Guide to Physical Activity at Work plus education through an information leaflet
Treatment:
Behavioral: Computer prompt "Stand up for your Health®"
Only Education (OE)
No Intervention group
Description:
The control group will receive only education through an information leaflet also following the guidelines of the Work Physical Activity Guide on indications to control the time sitting at work.

Trial contacts and locations

1

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Central trial contact

Barbara M Munoz Monari, Master; Jaime E Leppe Zamora, PhD©

Data sourced from clinicaltrials.gov

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