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CompletedNCT05522933Updated Mar 30, 2025

Development and Evaluation of an Online Multidimensional Musculoskeletal Health Programme

An interventional study of 4 weekly musculoskeletal health promotion workshops with stretching and muscle-strengthening exercise in Occupational Health, sponsored by The Hong Kong Polytechnic University. Completed at 1 site in Hong Kong. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-03-30.

Sponsored by The Hong Kong Polytechnic University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

Globally, work-related musculoskeletal symptoms (WRMSs) have become one of the major public health issues, with musculoskeletal problems contributing to the largest proportion of lost work productivity. Literature has reported that grassroots working-class workers (also known as low-skilled workers) are the most vulnerable group to WRMSs as their work mostly exposes them to the identified risk factors. However, not many intervention studies have been conducted for low-skilled workers to prevent WRMSs.

Based on the concept of the multidimensional approach from the literature, and the project team's previous evidence-based research results, this project will modify the project team's face-to-face evidence-based musculoskeletal health promotion program to an online mode with 4 weekly 45-minute workshops for low-skilled workers in the community under the Covid-19 pandemic situation. Thus, the project has the following specific objectives:

(i) To determine the feasibility of conducting the proposed online program (ii) To examine the acceptability and satisfaction of the online program from the workers' perspectives (iii) To evaluate the potential effects of the online program on the primary outcomes: compliance with exercise regimes, improvement of musculoskeletal literacy, and reduction of the number of body parts with WRMSs (iv) To evaluate the potential effects of the online program on the secondary outcomes: reduction of adverse workstyle, improvement of exercise self-efficacy, mental health, body mass index, hip-waist ratio, and blood pressure measurements

02

Conditions studied

  • Occupational Health
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In context

Lead sponsor

The Hong Kong Polytechnic University is the lead sponsor of 659 studies on the registry; 250 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • low-skilled workers aged ≥ 18
  • working full-time or part-time,
  • with at least one body part that had been affected by WRMSs for at least one month.

Exclusion criteria

Exclusion Criteria:

  • engagement in WRMS prevention programs in the workplace at the time of the study,
  • undergoing medical treatment
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Musculoskeletal Health

    The intervention group will receive the 4 weekly workshops

    Other: 4 weekly musculoskeletal health promotion workshops with stretching and muscle-strengthening exercise

Interventions

  • Other4 weekly musculoskeletal health promotion workshops with stretching and muscle-strengthening exercise

    The modified online multidimensional musculoskeletal health promotion program will consist of 4 weekly workshops for 90-minute each for a group size of 8-12 participants. The topics of the workshop are: (1) exercise and health \& work; (2) prevention of musculoskeletal problems; (3) musculoskeletal health and traditional Chinese medicine; and (4) mental health and community resources. Each workshop will consist of stretching and muscle strengthening exercises (30 minutes), a health education topic (about 45 minutes), and a question-and-answer period (about 15 minutes).

06

What researchers measure

Primary outcomes

  1. Compliance with exercise regimes

    Exercise regimes will be measured by number of times the participant perform the exercise taught. The higher the number represents a better outcome

    Time frame: Change from the measurement at baseline (T0) to one week after intervention (T1)

  2. Musculoskeletal literacy

    Musculoskeletal literacy will be measured by a scale with 25 items with right or wrong answer. Score 1 will be denoted to right answer while score 0 will be denoted to wrong answer. Thus, the higher the score represents a better outcome

    Time frame: Change from the measurement at baseline (T0) to one week after intervention (T1)

  3. Incidence of body parts with work-related musculoskeletal systems (WRMSs)

    The incidence of body parts with WRMSs will be measured by a modified general Nordic Musculoskeletal questionnaire to collect data about pain, aches or discomfort in different body parts. Score 1 will be denoted to one body part with WRMSs and Score 0 will be denoted to the body part without WRMSs. Thus, the higher the score represents a worse outcome.

    Time frame: Change from the measurement at baseline (T0) to one week after intervention (T1)

Secondary outcomes

  1. Adverse workstyle

    Adverse workstyle will be measured by a 24-item Chinese Workstyle Short Form for WRMSs with a 5-point Likert scale (0 = almost never and 4 = almost always). It consists of 4 subscales: work through pain (6 items), social reactivity (4 items), demands at work (12 items), and break (2 items). The sums of the subscales are used, the higher the score, the higher frequency of adverse workstyle practices (i.e., the worse of the outcome).

    Time frame: Change from the measurement at baseline (T0) to one week after intervention (T1)

  2. Self-efficacy

    The exercise self-efficacy will be measured by a 10-item self-efficacy scale with a 4-point-Likert scale (0=completely inaccurate to 3=completely accurate). The higher the score, the higher levels of self-efficacy (i.e., the better outcome)

    Time frame: Change from the measurement at baseline (T0) to one week after intervention (T1)

  3. Mental health

    Mental health will be measured by a 21-item depression, anxiety and stress scale (DASS) with a 4-point Likert scale (0=not applicable and 3 = very often). The higher the score represents a worse outcome.

    Time frame: Change from the measurement at baseline (T0) to one week after intervention (T1)

  4. Body mass index

    Body mass index will be calculated based on the measurement of height (meter) and weight (kilogram) with the formula of kg/m\^2. The higher the score represent a worse outcome.

    Time frame: Change from the measurement at baseline (T0) to one week after intervention (T1)

  5. Hip-waist ratio

    Hip-waist ratio will be calculated based on the measurement of hip and waist circumferences (inches) with the formula of waist circumference / hip circumference. The higher the score represents the worse outcome.

    Time frame: Change from the measurement at baseline (T0) to one week after intervention (T1)

  6. Blood pressure

    Blood pressure will be measured by both systolic and diastolic blood pressure. The higher the systolic pressure represents a worse outcome. Also, the higher the diastolic pressure represents a worse outcome.

    Time frame: Change from the measurement at baseline (T0) to one week after intervention (T1)

  7. Social support and exercise

    Social support and exercise will be measured by a 10-item scale with 5-point Likert scale (0=never, and 4=very often). The sum score will be used, the higher the score represents a better outcome.

    Time frame: Change from the measurement at baseline (T0) to one week after intervention (T1)

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Study locations

1 site
  • Residents Mutual Help Centre
    Kowloon, Hong Kong
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 30, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05522933
Lead sponsor
The Hong Kong Polytechnic University
Responsible party
Sponsor
First posted
Aug 31, 2022
Start date
Aug 18, 2022
Primary completion
May 31, 2023
Completion
Jan 31, 2025
Last update
Mar 30, 2025

Study contacts

Kin Cheung
principal investigator · The Hong Kong Polytechnic University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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