Online Yoga for Improving the Well-being of Desk-based Workers

February 26, 2024 updated by: Kingston University

The Effectiveness of a Yoga Intervention in Improving the Wellbeing and Productivity of Desk-based Workers

The goal of this clinical trial is to evaluate the effectiveness of an 8-week online yoga intervention in improving the well-being and productivity of desk-based workers. The main questions it aims to answer are:

  • How effective is an 8-week online yoga intervention in improving the well-being (mental and physical) and productivity (work engagement and job performance) of the yoga group compared with passive controls?
  • Are there any differences in well-being and work-related measures between the yoga and control groups?

Participants in the yoga group will practice yoga three days a week for 8 weeks and will be compared with a wait-listed control group, which will continue with the usual routine for 8 weeks. Researchers will evaluate the impact of yoga on the well-being and productivity of desk-based workers.

Study Overview

Detailed Description

Office workers are reported to spend 75% of their working day sitting (Mansoubi et al., 2016) and up to 10 hours across the whole day on workdays (Clemes et al., 2014). This presents a significant challenge to workforce well-being because of the increasing prevalence of remote work globally. A recent survey by the Office for National Statistics found that as of November 2022, the top four sectors in the UK using, or intending to use, increased homeworking as a permanent business model were those consisting of desk-based or office workers as their employees; viz information and communication (43.3%), professional scientific and technical activities (29.4%), education (17.2%), and administrative and support service activities (14.3%) (Office for National Statistics (ONS), 2022).

The most common problems among desk-based workers compared to any other occupational groups include the musculoskeletal symptoms of the neck and shoulders, wrists and hands, lower back, and upper extremities (AlOmar et al., 2021; Basakci Calik et al., 2022; Besharati et al., 2020; Bontrup et al., 2019; Mohammadipour et al., 2018). Furthermore, high sedentary behaviour is also associated with a greater risk of anxiety (Teychenne et al., 2015), depression (Hallgren et al.; Wang et al., 2019), perceived stress, particularly in white-collar employees (Dėdelė et al., 2019), adverse mental health (Hamer et al., 2014), lower job satisfaction and greater fatigue (Rosenkranz et al., 2020). Office workers, in particular, have been found to have a higher prevalence of common mental health disorders compared to other occupations in the UK (Stansfeld et al., 2011). Work-related ill health is also a significant concern for employers because of the productivity loss resulting in a substantial financial burden to the organizations (Griffiths et al., 2011; Johnston et al., 2008).

Yoga has been accepted as a holistic practice similar to mindfulness with the added advantage of components like postures (asana) and breathing practices (pranayama), providing physical, mental, emotional, social, and spiritual benefits (Gordon, 2013; Vergeer et al., 2021). As a multi-component practice, yoga can provide a holistic approach to managing the consequences of prolonged desk-based work. It appears to be a suitable and safe therapy that may improve pain and functional outcomes connected to a range of musculoskeletal conditions in a clinically relevant manner (Ward et al., 2013). Yoga has also shown positive effects on the mental health of various employee types, including office workers, as per two systematic reviews and a meta-analysis (Valencia et al., 2019; Valle et al., 2020). The rising prevalence of desk-based work and its likelihood of representing a larger proportion of the future workforce underlines the timeliness of this study.

Therefore, the study aims to explore the effectiveness of an 8-week yoga intervention in improving the well-being (mental and physical) and productivity (work engagement and job performance) of the yoga group compared with passive controls.

Study Type

Interventional

Enrollment (Estimated)

80

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 Contact

Study Locations

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. Participants working remotely/hybrid aged 18 years and above.
  2. living and working in the UK.
  3. speak and understand English.
  4. Fulfil the health criteria (e.g., No current injuries ).
  5. Are willing to commit to an 8-week online streamed yoga course, three times a week, 60 min each session

Exclusion Criteria:

  1. Current yoga practice or related activities.
  2. Medical or psychiatric conditions limiting the practice of yoga in general
  3. Not suffering from any serious medical or psychiatric illness.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Yoga - Group S
The experimental group will participate in 8 weeks of live online yoga classes, 3 times a week for 60 minutes each session. The yoga program will be designed based on previous evidence and personal experience of yoga experts and researchers.
The yoga program will consist of body awareness, meditation, poses, breathing practices, relaxation, and positive affirmations in Sanskrit and English.
No Intervention: Control - Group L
The control group will be waitlisted and will continue with the usual routine for 8 weeks. They will participate in 8-week yoga classes after the completion of the study.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perceived Stress Scale
Time Frame: 8 Weeks
The questions in this scale ask about your feelings and thoughts during the last month. In each case, you will be asked to indicate how often you felt or thought a certain way.
8 Weeks
PROMIS-Anxiety Short form
Time Frame: 8 Weeks
The 7-item PROMIS Anxiety Short Form assesses the pure domain of anxiety in individuals age 18 and older.
8 Weeks
The Short Warwick-Edinburgh Mental Well-being Scale (SWEMWBS)
Time Frame: 8 Weeks
The SWEMWBS is a short version of the Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS). The WEMWBS was developed to enable the monitoring of mental wellbeing in the general population and the evaluation of projects, programmes and policies which aim to improve mental wellbeing.
8 Weeks
The Mindful Attention Awareness Scale (MAAS)
Time Frame: 8 Weeks
The trait MAAS is a 15-item scale designed to assess a core characteristic of mindfulness, namely, a receptive state of mind in which attention, informed by a sensitive awareness of what is occurring in the present, simply observes what is taking place.
8 Weeks
The Cornell Musculoskeletal Discomfort Questionnaire (CMDQ)
Time Frame: 8 Weeks
The Cornell questionnaire was used to determine the level of pain among office employees in response to rest breaks and ergonomic modifications. Musculoskeletal discomforts, particularly pain severity among office employees, can be collected by the Cornell questionnaire shown to be a valid and reliable tool.
8 Weeks
Self-Compassion Scale Short Form (SCS-SF)
Time Frame: 8 Weeks
The Self-Compassion Scale - Short Form (SCS-SF) is a 12-item self-report measure that is used by adults to measure their capacity for self-compassion - the ability to hold one's feelings of suffering with a sense of warmth, connection and concern.
8 Weeks
The Compassion Scale (CS)
Time Frame: 8 Weeks
The CS has the same general structure as the SCS and measures compassion for others.
8 Weeks
Uterecht Work Engagment Scale-Short Form (UWES -9)
Time Frame: 8 Weeks

The UWES utilizes three scales to determine the level of work engagement:

Vigor, dedication, and absorption. It is a test of how to measure work engagement both on an individual and on group level: vigor, dedication, and absorption.

8 Weeks
Work Ability Index (WAI)
Time Frame: 8 Weeks
It measures current work ability compared to highest work ability ever.
8 Weeks
Center for Epidemiologic Studies Short Depression Scale (CES-D-R 10)
Time Frame: 8 Weeks
This scale is a self-report measure of depression.
8 Weeks
Heart Rate Variability (HRV)
Time Frame: 8 Weeks
HRV is simply a measure of the variation in time between each heartbeat. This variation is controlled by a primitive part of the nervous system called the autonomic nervous system (ANS). It works behind the scenes, automatically regulating our heart rate, blood pressure, breathing, and digestion among other key tasks. But in recent years, companies have launched apps and wearable heart rate monitors that monitor HRV. We are using a Polar H10 heart rate sensor to measure HRV of participants to see physiological changes in stress levels due to practising yoga.
8 Weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Vipin Wadhen, MPhil, Kingston University

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 (Actual)

February 15, 2024

Primary Completion (Estimated)

August 15, 2024

Study Completion (Estimated)

August 15, 2024

Study Registration Dates

First Submitted

February 26, 2024

First Submitted That Met QC Criteria

February 26, 2024

First Posted (Estimated)

March 1, 2024

Study Record Updates

Last Update Posted (Estimated)

March 1, 2024

Last Update Submitted That Met QC Criteria

February 26, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • KU3339

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

All IPD that underlie results in a publication.

IPD Sharing Time Frame

July 2025

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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