Skip to main content
Clinical Trials/NCT04053686
NCT04053686
Completed
Not Applicable

A-REST (Activity to Reduce Excessive Sitting Time): a Cluster Randomised Controlled Feasibility Trial to Reduce Prolonged Sitting in Police Staff

University of Bedfordshire1 site in 1 country24 target enrollmentSeptember 9, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sedentary Behavior
Sponsor
University of Bedfordshire
Enrollment
24
Locations
1
Primary Endpoint
Feasibility - Acceptability: Perceptions of the intervention
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The primary aim of this study is to assess the feasibility of an intervention to reduce and break up prolonged sitting time in full-time police staff. The secondary aims of this study are to assess preliminary effects on patterns of sedentary behaviour (number of breaks, number of prolonged sitting bouts, average duration of prolonged sitting bouts, and total prolonged sitting duration), additional measures of sedentary behaviour (total sitting time, standing, and stepping), cardiometabolic risk markers, physiological stress (cortisol levels), physical health (self-report and postural stability), psychological wellbeing and mood, work stress (self-reported), and work performance (job satisfaction and productivity).

Detailed Description

Prolonged sedentary behaviour is associated with a higher incidence of cardiovascular disease and type 2 diabetes. A large proportion of daily sedentary time (sitting) occurs in the workplace. On average, full time office workers spend upwards of 70% of their working day seated with the majority of this time accumulated in sitting bouts ≥ 20 minutes. A recent cross-sectional investigation into the occupational characteristics of over 5,000 British police force employees reported at least 30% identifying as having mainly office-based duties. When trying to reduce prolonged sitting in the workplace, one of the most effective strategies is the use of multi-component interventions. At the present time, sedentary workplace intervention studies in the police are limited. The primary aim of this study is to assess the feasibility of an intervention to reduce and break up prolonged sitting time at work in full-time police staff. The secondary aims of this study are to assess preliminary effects on sedentary behaviour, cardiometabolic risk markers, physiological stress, physical health, psychological wellbeing and mood, work stress, and work performance. This has a single-arm, pre-post study design. Participants will receive a multi-component intervention to break up and reduce prolonged sitting including: a presentation/workshop, electronic support, minor environmental modifications, organisational support, and team competition. Assessments will take place at baseline and post-intervention (week 10).

Registry
clinicaltrials.gov
Start Date
September 9, 2019
End Date
December 20, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marsha Brierley

PhD Student

University of Bedfordshire

Eligibility Criteria

Inclusion Criteria

  • ≥ 0.6 Full Time Equivalent (FTE) work hours
  • Ambulatory
  • Predominantly desk-based (spend on average ≥ 5-h/day seated at work by self-report)
  • Own a smartphone, with ability to keep phone with them during work hours

Exclusion Criteria

  • Planned absence of two weeks or more during the intervention period
  • Work part time (\< 0.6 FTE)
  • Health contraindications to standing and walking
  • Planned relocation to another site, office or workplace
  • Have personal access to an active workstation (sit-stand desk, seat cycle, treadmill desk or similar)
  • Participating simultaneously in another workplace intervention (for sedentary behaviour, physical activity, diet, lifestyle, or combination thereof)
  • Health contraindications to postural stability testing (e.g., injury to the lower extremities in the past six months, dizziness, or epilepsy)

Outcomes

Primary Outcomes

Feasibility - Acceptability: Perceptions of the intervention

Time Frame: At week 11

Asking participants' to qualitatively reflect on the intervention via semi-structured interview.

Feasibility - Adherence: Drop-out rates in control and intervention group

Time Frame: From recruitment (typically 4 weeks prior to baseline) up to study completion (typically 12 weeks)

Analyses of drop-out rates (%) in control and intervention group.

Secondary Outcomes

  • Lean body mass (kg)(Baseline and at week 11)
  • Fasted blood cholesterol (mg/dL)(Baseline and at week 11)
  • Fasted blood glucose (mg/dL)(Baseline and at week 11)
  • Change in the number of breaks (sit-stand transitions) from sedentary time per hour (workplace and daily)(This measure will be assessed at baseline and 10 weeks. At each time point the accelerometer will be worn for 7 days.)
  • Change in the number of prolonged sitting bouts (≥ 30 minutes) (workplace and daily)(This measure will be assessed at baseline and 10 weeks. At each time point the accelerometer will be worn for 7 days.)
  • Change in total standing time (in minutes) (workplace and daily)(This measure will be assessed at baseline and 10 weeks. At each time point the accelerometer will be worn for 7 days.)
  • Change in sitting time accrued in prolonged bouts (≥ 30 minutes) (workplace and daily)(This measure will be assessed at baseline and 10 weeks. At each time point the accelerometer will be worn for 7 days.)
  • Change in step count (workplace and daily)(This measure will be assessed at baseline and 10 weeks. At each time point the accelerometer will be worn for 7 days.)
  • Weight (kg)(Baseline and at week 11)
  • Nordic musculoskeletal questionnaire(Baseline and at week 11)
  • Postural sway range (mm)(Baseline and at week 11)
  • Change in the average duration (minutes) of prolonged sitting bouts (≥ 30 minutes) (workplace and daily)(This measure will be assessed at baseline and 10 weeks. At each time point the accelerometer will be worn for 7 days.)
  • Change in total stepping time (in minutes) (workplace and daily)(This measure will be assessed at baseline and 10 weeks. At each time point the accelerometer will be worn for 7 days.)
  • Body fat %(Baseline and at week 11)
  • Change in the total duration (minutes) of sitting time (workplace and daily)(This measure will be assessed at baseline and 10 weeks. At each time point the accelerometer will be worn for 7 days.)
  • Body mass index (BMI)(Baseline and at week 11)
  • Blood pressure (mmHg)(Baseline and at week 11)
  • Fasted blood triglycerides (mg/dL)(Baseline and at week 11)
  • Warwick-Edinburgh mental well-being scale (WEMWBS)(Baseline and at week 11)
  • Waist circumference (cm)(Baseline and at week 11)
  • Body fat mass (kg)(Baseline and at week 11)
  • Salivary cortisol (nmol/L)(Baseline and at week 11. At each time point saliva samples will be collected at 7 time points over the course of one day.)
  • Postural sway velocity (mm/s)(Baseline and at week 11)
  • Marshall sitting questionnaire(Baseline and at week 11)
  • Operational police stress questionnaire (PSQ-Op)(Baseline and at week 11)
  • International Physical Activity Questionnaire short form (IPAQ)(Baseline and at week 11)
  • Positive and negative affect schedule (PANAS)(Baseline and at week 11)
  • Organisational police stress questionnaire (PSQ-Org)(Baseline and at week 11)
  • Job satisfaction(Baseline and at week 11)
  • Job performance(Baseline and at week 11)

Study Sites (1)

Loading locations...

Similar Trials