Reduce Sedentariness and Enhance Psychological Well-being of Office Workers With TCM-based Intervention
1 other identifier
interventional
64
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 13, 2023
CompletedFirst Posted
Study publicly available on registry
December 27, 2023
CompletedStudy Start
First participant enrolled
March 20, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2024
CompletedJune 18, 2025
June 1, 2025
10 months
December 13, 2023
June 13, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
sedentary behavior- total sitting time/workday
measured by Actigraph wGT3X-BT
Baseline, week 5, week 9
sedentary behavior- sitting time/9-h working time
measured by Actigraph wGT3X-BT
Baseline, week 5, week 9
Self-report sedentary behaviors
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
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
physiological stress
measured by salivary cortisol concentration(measured in ng/mL)
Baseline, week 5, week 9
Secondary Outcomes (8)
Holistic thinking
Baseline
Health-related quality of life
Baseline, week 5, week 9
Sleep quality
Baseline, week 5, week 9
Psychological distress
Baseline, week 5, week 9
Self efficay
Baseline, week 5, week 9
- +3 more secondary outcomes
Study Arms (2)
TCM-based anti-sedentariness intervention group
EXPERIMENTALTCM-based anti-sedentariness intervention
Wait-list control group
OTHERAfter the completion of all evaluations, the intervention content will be administered to the experimental group in the same manner.
Interventions
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.
Eligibility Criteria
You may qualify if:
- Aged 18 or above with a full-time and office-based job
- Reported \>5.5 hours of sitting per day at work
- Native Chinese speaker (Cantonese or Mandarin)
- Be able to give consent
You may not qualify if:
- Have severe or chronic illness and not suitable for physical exercise
- Be oversensitive to tactile stimulation
- Have regular practice of qigong, acupressure, or mindfulness-based activities during the 4 weeks prior to recruitment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Hong Kong Polytechnic University
Hong Kong, Hong Kong, 999077, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Hector Tsang, PhD
The Hong Kong Polytechnic University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- Due to the nature of the experiment, participants will not be blinded. However, the intervention provider and the evaluator will be blinded.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Chair Professor
Study Record Dates
First Submitted
December 13, 2023
First Posted
December 27, 2023
Study Start
March 20, 2024
Primary Completion
December 30, 2024
Study Completion
December 31, 2024
Last Updated
June 18, 2025
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will not share