Reduce Sedentariness and Enhance Psychological Well-being of Office Workers With TCM-based Intervention

June 13, 2025 updated by: TSANG Hector Wing-Hong, The Hong Kong Polytechnic University

Reduce Sedentariness and Enhance Physical and Psychological Health of Office Workers With TCM-based Anti-sedentary Intervention: Efficacy and Potential Psychophysiological Mechanisms

The goal of this clinical trial is to test the effects of a TCM-based anti-sedentariness program on workplace sitting time, perceived stress, and cortisol in office workers.The main questions it aims to answer are:

  1. Can a Traditional Chinese Medicine (TCM)-based anti-sedentariness program effectively reduce workplace sitting time, perceived stress and cortisol levels among office workers?
  2. Whether such anti-sedentary effect works through stress management and enhances when holistic thinking is endorsed.

Participants will engage in a 4 week TCM-based program intervention including 2 weeks of health education and promotion activities (understanding sedentary behaviors, Baduanjin, acupressure, dantian breathing, and mindfulness) and 2 weeks of supported self-practice (daily reminders and tips, regular feedback on sitting time, and individual consultation).

Researchers will compare a group receiving a Traditional Chinese Medicine (TCM)-based intervention with a wait-list control group to determine the effectiveness of the intervention in reducing sitting time and enhancing physical and psychological health.

Study Overview

Status

Completed

Conditions

Detailed Description

Introduction:

Sedentary behaviors and their associated physical and mental health risks among adults have received growing concerns among the clinical and research communities. Office workers commonly engage in sedentary behaviors due to their long stationary hours. Evidence has revealed that higher levels of sedentary behaviors were associated with higher perceived stress levels at workplace. However, scarce studies focused on the role of stress management in reducing sedentary behaviors. Traditional Chinese medicine (TCM)-based body works (such as dantian breathing, qigong, and acupressure) are low-cost techniques and found to be primising in addressing stress and sedentary behaviors at workplace. The health benefits of TCM-based bodywork in sedentary office workers may be enhanced when the workers endorse holistic thinking.

The present research aims to test the effects of a TCM-based anti-sedentariness program on workplace sitting time, perceived stress, and cortisol in office workers. Investigators will also explore the psychophysiological mechanism whether such anti-sedentary effect works through stress management and enhances when holistic thinking is endorsed.

Methods:

A systematic review and meta-analysis has been conducted to synthesize the pooled effect of existing anti-sedentariness interventions on office workers' sitting time and compare the effectiveness of different intervention types in reducing sedentary behaviors relative to the control group. The systematic review and meta-analysis set the theoretical foundation of intervention elements for the reduction of sedentary behaviors at workplace and their psychological effects to be applied in the present study.

A randomized controlled trial will be conducted among 92 office workers with self-reported sitting time of 5.5 hours or longer per workday. Participants will be randomly assigned to intervention (TCM-based program) and wait-list control groups. The TCM-based program will last for 4 weeks, with 2 weeks of health education and promotion activities (understanding sedentary behaviors, Baduanjin, acupressure, dantian breathing, and mindfulness) and 2 weeks of supported self-practice (daily reminders and tips, regular feedback on sitting time, website support and individual consultation). Participants' sitting time per workday and perceived stress will be assessed at baseline, post-intervention (4 weeks after baseline), and follow-up (6 weeks after baseline). During the 2-week self-practice, participants in the intervention group will complete a diary of self-practice duration of TCM-based bodywork, perceived stress, and collect saliva samples every two days. Repeated-measures ANOVA will be used to test the group differences in changes in sitting time and perceived stress. Mediating effects of perceived stress and cortisol and moderating effects of holistic thinking will be explored through SPSS marcos.

Significance:

The findings of this study will provide valuable insights into the effectiveness of a TCM-based intervention in reducing sedentary behavior and improving psychological well-being. It is innovative to understand the psychophysiological mechanism of reducing sedentary behavior to explore tailored interventions to enhance the health quality of office workers. Given the easy practice and low cost of the TCM-based body works, the project can put forward a cost-effective intervention that can benefit a large population sustainably.

Study Type

Interventional

Enrollment (Actual)

64

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

    • Hong Kong
      • Hong Kong, Hong Kong, China, 999077
        • The Hong Kong Polytechnic University

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. Aged 18 or above with a full-time and office-based job
  2. Reported >5.5 hours of sitting per day at work
  3. Native Chinese speaker (Cantonese or Mandarin)
  4. Be able to give consent

Exclusion Criteria:

  1. Have severe or chronic illness and not suitable for physical exercise
  2. Be oversensitive to tactile stimulation
  3. Have regular practice of qigong, acupressure, or mindfulness-based activities during the 4 weeks prior to recruitment

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: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: TCM-based anti-sedentariness intervention group
TCM-based anti-sedentariness intervention

Week1-2: one health talk session(60 mins); three workshops (each workshop will last for 60-90mins) to provide hands-on training in Baduanjin, acupressure techniques, mindful stretching, and effective strategies to combat sedentary behavior in the workplace.

Week 3-4: group practice sessions will take place for one hour every other day throughout the workweek; website support.

Other Names:
  • TCM-based program
Other: Wait-list control group
After the completion of all evaluations, the intervention content will be administered to the experimental group in the same manner.

Week1-2: one health talk session(60 mins); three workshops (each workshop will last for 60-90mins) to provide hands-on training in Baduanjin, acupressure techniques, mindful stretching, and effective strategies to combat sedentary behavior in the workplace.

Week 3-4: group practice sessions will take place for one hour every other day throughout the workweek; website support.

Other Names:
  • TCM-based program

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
sedentary behavior- total sitting time/workday
Time Frame: Baseline, week 5, week 9
measured by Actigraph wGT3X-BT
Baseline, week 5, week 9
sedentary behavior- sitting time/9-h working time
Time Frame: Baseline, week 5, week 9
measured by Actigraph wGT3X-BT
Baseline, week 5, week 9
physiological stress
Time Frame: Baseline, week 5, week 9
measured by salivary cortisol concentration(measured in ng/mL)
Baseline, week 5, week 9
Self-report sedentary behaviors
Time Frame: Baseline, week 5, week 9
measured by International Physical Activity Questionnaire (IPAQ short version) with 8 items. Physical activity levels can be classified as low intensity when the weekly MET (metabolic equivalent of task) value is less than 600, moderate intensity when it ranges from 600 to 3000 MET, and high intensity when it exceeds 3000 MET per week.
Baseline, week 5, week 9
psychological stress
Time Frame: Baseline, week 5, week 9
measured by perceived stress scale(PSS) with 10 items. Each item in the PSS questionnaire is rated on a five-point Likert scale, ranging from 0 (never) to 4 (very often). Participants are asked to indicate the frequency with which they have experienced each event over the past month.The total score on the PSS can range from 0 to 40. Higher scores indicate a higher level of perceived stress.
Baseline, week 5, week 9

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Health-related quality of life
Time Frame: Baseline, week 5, week 9
measured by The Chinese (Hong Kong) SF-36 Health Survey. It consists of 36 questions that cover eight different domains: physical functioning, role limitations due to physical health problems, bodily pain, general health perceptions, vitality, social functioning, role limitations due to emotional problems, and mental health. A higher score indicates better quality of life.
Baseline, week 5, week 9
Sleep quality
Time Frame: Baseline, week 5, week 9
measured by The Pittsburgh Sleep Quality Index, PSQI.The Pittsburgh Sleep Quality Index consists of 19 individual items, with a total score of 21 and a higher score indicating poorer sleep quality.
Baseline, week 5, week 9
Psychological distress
Time Frame: Baseline, week 5, week 9
measured by Depression Anxiety Stress Scale(DASS).The DASS-21 consists of 21 items, with seven items dedicated to each of the three subscales: depression, anxiety, and stress. A higher score indicates more depression, anxiety and stress.
Baseline, week 5, week 9
Self efficay
Time Frame: Baseline, week 5, week 9
measured by The Chinese Self-Efficacy Scale. It consists of 10 items.The total score is calculated by finding the sum of the all items. For the GSE, the total score ranges between 10 and 40, with a higher score indicating more self-efficacy.
Baseline, week 5, week 9
Hand grip strength
Time Frame: Baseline, week 5, week 9
measured by Jamar handheld dynamometer
Baseline, week 5, week 9
IL-6
Time Frame: Baseline, week 5, week 9
Collect saliva samples to assay IL-6 concentration by using enzyme-linked immunoassay according to the manufacturer's instruction.
Baseline, week 5, week 9
Blood pressures
Time Frame: Baseline, week 5, week 9
Systolic and diastolic blood pressure will be measured by Omron blood pressure monitor.
Baseline, week 5, week 9
Holistic thinking
Time Frame: Baseline
measured by Analysis-Holism Scale (AHS), which consists of 24 items. Items are rated on a scale ranging from 1 to 7 (1 = strongly disagree, 7 = strongly agree). The total score on the AHS can range from 24 to 168. Higher scores indicate greater holistic cognitive style, and lower scores indicate greater analytic cognitive style.
Baseline

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Hector Tsang, PhD, The Hong Kong Polytechnic 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)

March 20, 2024

Primary Completion (Actual)

December 30, 2024

Study Completion (Actual)

December 31, 2024

Study Registration Dates

First Submitted

December 13, 2023

First Submitted That Met QC Criteria

December 13, 2023

First Posted (Actual)

December 27, 2023

Study Record Updates

Last Update Posted (Actual)

June 18, 2025

Last Update Submitted That Met QC Criteria

June 13, 2025

Last Verified

June 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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