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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04783454
Acronym
Prevent@HOME
Enrollment
600
Registered
2021-03-05
Start date
2020-11-12
Completion date
2028-12-31
Last updated
2023-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Back Pain, Low Back Pain, Neck Pain

Keywords

desktop workers, telework, remote work, sedentary work, primary prevention

Brief 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

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).

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)

Sponsors

University Ghent
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

All investigators and outcome assessors are blind to the subjects' allocation

Eligibility

Sex/Gender
ALL
Age
18 Years to 69 Years
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

* 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

Design outcomes

Primary

MeasureTime frameDescription
neck pain1 yearDid you develop neck pain (YES or NO)
low back pain1 yearDid you develop low back pain (YES or NO)

Secondary

MeasureTime frameDescription
time to exposure1yearamount of desktop work (hours/week)
global perceived effect1yearWhat is your global perceived effect of the intervention program (NRS - score/100)
use of (pain) medication and/or (para)medical care1yearuse of (pain) medication and/or (para)medical care (name, dosage/frequency, effect, prescribed or direct acces)
behavioral change1 yearTendency 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)
36-Item Short Form Health Survey (SF-36 questionnaire)1yearquality 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)
Insomnia severity index (ISI questionnaire)1yearquality 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)
Depression Anxiety Stress Scale-21 (DASS-21 questionnaire)1yearfear, 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)
physical activity (Baecke Questionnaire)1yearphysical 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)

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026