NCT06183125

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. 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. 2.Whether such anti-sedentary effect works through stress management and enhances when holistic thinking is endorsed.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
64

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
14 days until next milestone

First Posted

Study publicly available on registry

December 27, 2023

Completed
3 months until next milestone

Study Start

First participant enrolled

March 20, 2024

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2024

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
Last Updated

June 18, 2025

Status Verified

June 1, 2025

Enrollment Period

10 months

First QC Date

December 13, 2023

Last Update Submit

June 13, 2025

Conditions

Keywords

sedentary behavioroffice workerTraditional Chinese MedicineRCTpsychophysiological mechanism

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

EXPERIMENTAL

TCM-based anti-sedentariness intervention

Behavioral: Traditional Chinese Medicine-based program

Wait-list control group

OTHER

After the completion of all evaluations, the intervention content will be administered to the experimental group in the same manner.

Behavioral: Traditional Chinese Medicine-based program

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.

Also known as: TCM-based program
TCM-based anti-sedentariness intervention groupWait-list control group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Sedentary Behavior

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Hector Tsang, PhD

    The Hong Kong Polytechnic University

    PRINCIPAL INVESTIGATOR

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
Model Details: A randomized controlled trial will be conducted among 64 office workers with self-reported sitting time of 5.5 hours or longer per workday. They will be randomly assigned to intervention (TCM-based program) and wait-list control groups.
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

Locations