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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT03678623




Registration number
NCT03678623
Ethics application status
Date submitted
9/09/2018
Date registered
19/09/2018

Titles & IDs
Public title
The Impact of Prolonged Standing on Musculoskeletal Pain
Scientific title
Exploring the Impact of Standing on the Musculoskeletal System of Sedentary-workers
Secondary ID [1] 0 0
Standing-musculoskeletal pain
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Musculoskeletal Pain 0 0
Occupational Exposure 0 0
Office Workers 0 0
Condition category
Condition code
Musculoskeletal 0 0 0 0
Other muscular and skeletal disorders

Intervention/exposure
Study type
Observational
Patient registry
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
Office-based workers - Individuals working in an office environment with their main tasks involving use of a computer, reading, phoning, making presentations and participating in meetings, who perform more than 30 hours per week mostly sitting at a computer.
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Standing Tolerance Test (STT)
Timepoint [1] 0 0
Baseline
Secondary outcome [1] 0 0
Demographic characteristics:
Timepoint [1] 0 0
Baseline
Secondary outcome [2] 0 0
Occupational characteristics: Occupational Sitting and Physical Activity Questionnaire (OSPAQ)
Timepoint [2] 0 0
Baseline
Secondary outcome [3] 0 0
Occupational characteristics: questions about using sit-stand workstation
Timepoint [3] 0 0
Baseline
Secondary outcome [4] 0 0
Occupational characteristics: Abbreviated Job Content Questionnaire (JCQ) & Job Satisfaction
Timepoint [4] 0 0
Baseline
Secondary outcome [5] 0 0
International Physical Activity Questionnaire (IPAQ)-Short Form
Timepoint [5] 0 0
Baseline
Secondary outcome [6] 0 0
Quality of life related to health: SF12 questionnaire
Timepoint [6] 0 0
Baseline
Secondary outcome [7] 0 0
Prevalence of musculoskeletal pain: Nordic Musculoskeletal Questionnaire (NMQ)
Timepoint [7] 0 0
Baseline
Secondary outcome [8] 0 0
Symptom intensity level of musculoskeletal pain: Visual Analogue Scale (VAS)
Timepoint [8] 0 0
Baseline
Secondary outcome [9] 0 0
Disability due to low back pain:
Timepoint [9] 0 0
Baseline
Secondary outcome [10] 0 0
Catastrophizing thoughts related with pain
Timepoint [10] 0 0
Baseline
Secondary outcome [11] 0 0
Thoracic and lumbar curve
Timepoint [11] 0 0
Baseline
Secondary outcome [12] 0 0
Motor Control Impairment test: Active hip abduction test
Timepoint [12] 0 0
Baseline
Secondary outcome [13] 0 0
Motor Control Impairment test: Active straight leg raise test
Timepoint [13] 0 0
Baseline
Secondary outcome [14] 0 0
Motor Control Impairment test: Prone knee flexion test
Timepoint [14] 0 0
Baseline
Secondary outcome [15] 0 0
Endurance tests of the trunk muscles (McGill's protocol): Sorensen test
Timepoint [15] 0 0
Baseline
Secondary outcome [16] 0 0
Endurance tests of the trunk muscles (McGill's protocol): Abdominal endurance test
Timepoint [16] 0 0
Baseline
Secondary outcome [17] 0 0
Endurance tests of the trunk muscles (McGill's protocol): Side bridge test
Timepoint [17] 0 0
Baseline
Secondary outcome [18] 0 0
Endurance tests of the trunk and hip muscles: Supine Bridge Test
Timepoint [18] 0 0
Baseline
Secondary outcome [19] 0 0
Endurance tests of the hip muscles: Abductor Hip Endurance Test
Timepoint [19] 0 0
Baseline

Eligibility
Key inclusion criteria
* Office-based workers who perform more than 30 hours per week mostly sitting at a computer,
* With aged 18 or above.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
* not office-based workers,
* pregnant or less than six months postpartum,
* had experienced any major trauma or had surgery to the spine or lower limb over the last 12 months,
* had been diagnosed with any neurological or systematic pathology (such as rheumatoid arthritis, multiple sclerosis or ankyloses spondylitis).

Study design
Purpose
Duration
Selection
Timing
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
23/04/2018
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
30/09/2019
Sample size
Target
Accrual to date
Final
40
Recruitment in Australia
Recruitment state(s)
QLD
Recruitment hospital [1] 0 0
The University of Queensland - Brisbane
Recruitment postcode(s) [1] 0 0
4072 - Brisbane

Funding & Sponsors
Primary sponsor type
Other
Name
Universidade da Coruña
Address
Country
Other collaborator category [1] 0 0
Other
Name [1] 0 0
The University of Queensland
Address [1] 0 0
Country [1] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Venerina Johnston, PhD
Address 0 0
The University of Queensland
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.


Results not provided in https://clinicaltrials.gov/study/NCT03678623