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RecruitingNCT04783454Prevent@HOMEUpdated Nov 18, 2023

Preventing Neck & Back Pain in Teleworking Office Workers: a Randomized Controlled Trial

An interventional study of Exercise program in Neck Pain, Low Back Pain and Back Pain, sponsored by University Ghent. Recruiting at 1 site in Belgium. Open to participants aged 18 Years to 69 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-11-18.

Sponsored by University Ghent · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Nov 2020, registered Feb 2021).
  • Started Nov 2020; still recruiting 5 years 10 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
600
Allocation
Randomized
Ages
18 Years to 69 Years
Sex
All
01

Study summary

The purpose of this study is to assess the effect of a general training program and educational session to prevent neck and/or low back pain in desktop workers

Read the detailed description

After being informed about the study and potential risks, all subjects that met the preset inclusion criteria and gave written informed consent to participate will be randomized into an intervention or control group in a 1:1 ratio. Next, subjects of both groups will undergo baseline testing (online survey). The subjects of the intervention group receive a single educational video (online) and are motivated to follow 2 training sessions of 60 minutes each, during 12 consecutive weeks. Instructions for the specific exercises are provided via an online platform. The subjects of the control group are instructed to maintain their normal working activities and activities of daily life and receive no further intervention. Subjects of both groups are prompted to fill out a weekly online logbook to gather information on their physical activity and neck and/or back complaints. All subjects undergo post-intervention testing at 12 weeks (short term effects), 6 months, and 12 months (long term effects).

02

Conditions studied

  • Neck Pain
  • Low Back Pain
  • Back Pain

Keywords

  • desktop workers
  • telework
  • remote work
  • sedentary work
  • primary prevention
03

In context

Back Pain

2,373 studies on the registry are indexed under Back Pain; 284 are open to participants now.

This study's planned enrollment of 600 is above the median of 60 across 1,941 interventional studies indexed under Back Pain.

Browse Back Pain studies →

Lead sponsor

University Ghent is the lead sponsor of 345 studies on the registry; 85 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 69 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • age between 18-69 years
  • perform regular desktop work (at least 20 hours/week)
  • perform desktop work for at least 1 year (employee or student)

Exclusion criteria

Exclusion Criteria:

  • documented structural neck- and/or back pathology (confirmed by medical imaging)
  • known shoulder or vestibular pathology
  • whiplash-associated disorders
  • history of surgery in the neck, shoulder, hip, and/or back area
  • (history of) chronic pain condition
  • serious headache
  • serious cardiovascular/metabolic/systemic/neurological conditions
  • chronic fatigue syndrome
  • fibromyalgia
  • psychiatric conditions or history of serious depression
  • serious catastrophizing thoughts
  • pregnancy or delivery in the past year
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
600 participants (estimated)

Study arms

  • Experimental
    Intervention

    * single (online) educational video on how the prevention program is designed and general advice on (how to adopt) a healthy lifestyle * 12-week training program: 2 sessions of 60 minutes per week, with the focus of the first session on cardiovascular exercises, and the focus of the second session on mobility and strengthening exercises

    Other: Exercise program

  • No intervention
    control

    no intervention (wait and see approach)

Interventions

  • OtherExercise program

    educational video on training program design and healthy lifestyle 24 training sessions (12 on cardiovascular endurance training, 12 on mobility and strength)

06

What researchers measure

Primary outcomes

  1. neck pain

    Did you develop neck pain (YES or NO)

    Time frame: 1 year

  2. low back pain

    Did you develop low back pain (YES or NO)

    Time frame: 1 year

Secondary outcomes

  1. behavioral change

    Tendency to remain physically active (PA) during working hours as compared to before your participation in this study (Likert-type scale: not at all PA - slightly less PA - equally PA - slightly more PA - clearly more PA)

    Time frame: 1 year

  2. physical activity (Baecke Questionnaire)

    physical activity measurement (activities are scored on a scale of 1-5 with the total scored from 3-15. the lower the score, the less physically active)

    Time frame: 1year

  3. time to exposure

    amount of desktop work (hours/week)

    Time frame: 1year

  4. global perceived effect

    What is your global perceived effect of the intervention program (NRS - score/100)

    Time frame: 1year

  5. use of (pain) medication and/or (para)medical care

    use of (pain) medication and/or (para)medical care (name, dosage/frequency, effect, prescribed or direct acces)

    Time frame: 1year

  6. Depression Anxiety Stress Scale-21 (DASS-21 questionnaire)

    fear, depressive mood, and stress due to COVID-19 crisis and confinement (21 items, Each item is scored from 0 to 3 and is doubled so the global ISI score ranges from 0 to 42)

    Time frame: 1year

  7. 36-Item Short Form Health Survey (SF-36 questionnaire)

    quality of life during confinement and telework (item scores are summed to scale scores and transformed into a hundred point scale; scores are transformed so that a higher score indicates better health status)

    Time frame: 1year

  8. Insomnia severity index (ISI questionnaire)

    quality of sleep during confinement and telework (7 items, Each item is scored from 0 to 4 and the global ISI score ranges from 0 to 28)

    Time frame: 1year

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 18, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04783454
Lead sponsor
University Ghent
Responsible party
Sponsor
First posted
Mar 5, 2021
Start date
Nov 12, 2020
Primary completion
Nov 30, 2028 (estimated)
Completion
Dec 31, 2028 (estimated)
Last update
Nov 18, 2023

Oversight

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

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