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Workplace Exercise Intervention in Administrative Personnel to Reduce Spinal Pain

The Implementation of a Web-based Workplace Exercise Intervention in the Reduction of Spinal Pain in Sedentary Administrative Personnel: Protocol of a Mixed Methodology Study.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05571124
Enrollment
66
Registered
2022-10-07
Start date
2023-10-01
Completion date
2024-12-31
Last updated
2023-12-05

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

Conditions

Back Pain, Sedentary Behavior

Keywords

Back Pain, Health Education, Therapeutic Exercise, Sedentary Behavior

Brief summary

The goal of this Clinical trial is to compare treatments in sedentary administrative personnel with back pain. The main question it aims to answer: The benefits of a workplace intervention with therapeutic exercise and pain education compared with only therapeutic exercise intervention Participants will perform active pauses in their workplace with a web-based program that consists of videos or images of exercises and pain education information. Researchers will compare a group Therapeutic exercise and pain education intervention with a group therapeutic exercise only to see if pain education plus exercise is a more beneficial intervention in reducing back pain in symptomatic administrative personnel.

Detailed description

Introduction: Musculoskeletal pathologies are one of the leading causes of disability for the population worldwide, with office workers being one of the most affected groups. This study aims to design and implement a programme of therapeutic exercise and pain education in the workplace to reduce musculoskeletal pathology. The use of therapeutic exercise interventions at work is an economical and feasible option in which it is essential to consider biopsychosocial aspects when designing a successful treatment. Methods: Mixed methodology study. Phase 1: A qualitative study with a phenomenological approach using semi-structured interviews to determine factors related to office workers' expectations about pain, maintaining static postures at work and implementing active breaks. Phase 2: Implementation of a Randomised Controlled Trial considering current scientific evidence and the results of the first phase with two intervention groups. A group in which therapeutic exercise will be performed at work with pain education, compared to a group implementing only exercise at the workplace. Discussion: This study is a comprehensive and pragmatic intervention to implement therapeutic exercise in the workplace, considering workers' expectations regarding their pain and the implementation of active breaks. The use of digitalisation in the implementation of therapeutic exercise and pain education in office workers is a feasible and low-cost option. It can improve office workers' quality of life by increasing motivation and adherence to such interventions.

Interventions

BEHAVIORALTherapeutic Exercise Intervention

Participants will perform stretching and mobility exercises in short bouts of time.

Sponsors

Universitat de Lleida
Lead SponsorOTHER

Study design

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

Masking description

To ensure that allocation is concealed, one of the researchers will randomly create the codes in opaque envelopes with the username and password for participants to log into the web platform. The evaluators will be blinded to the data collection as each participant will be assigned a code for identification. The participants will not be blinded as they are aware of the intervention they are carrying out.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* More than 80% of the working day is in a seated position. * Workers who have a computer or mobile device with an internet connection. * Workers with more than three months of pain in the back area due to a non-specific cause.

Exclusion criteria

- * Part-time workers. * Pathologies that cause chronic pain. * Radiculopathies or symptomatic disc herniations/protrusions. * Inability to perform low-moderate intensity exercise. * People who are active in their daily lives outside of work willing to report that they meet the minimum stipulated by the WHO (a minimum of 10,000 steps per day and 75-150 minutes of vigorous-moderate physical activity per week). * Undergoing physiotherapy treatment through public health or a private company. * Workers on sick leave or during pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Reduction of Back PainChange from baseline back pain at six weeksThe primary outcome to be analysed is back pain using the Visual Analogue Scale, a subjective assessment scale of intensity from 0 to 10, with 0 being no pain and 10 being the worst possible pain.

Secondary

MeasureTime frameDescription
Back pain dysfunctionChange from baseline back pain dysfunction at six weeksWill be analysed using the Spanish version of the Spine Functional Index, a self-administered questionnaire in which the patient reports the state of his or her back concerning disability and dysfunction in daily activities.
Health related quality of lifeChange from baseline quality of life at six weeksWill be analysed using the Spanish version of the EQ-5D-5L quality of life questionnaire which consists of 5 dimensions: mobility, self-care, activities of daily living, pain/discomfort and anxiety/depression.
Motivation of performing therapeutic exerciseChange from baseline motivation of performing therapeutic exercise at six weeksMotivation when performing the therapeutic exercise intervention will be analysed using the Spanish version of the questionnaire: Behavioural Regulation in Exercise Questionnaire-2.
Adherence to therapeutic exerciseThrough study completion, an average of six weeksThe percentage of open sessions and total video played of the participant will be analysed by the web analytics.

Countries

Spain

Contacts

Primary ContactCarlos Tersa Miralles, PhD student
carles.tersa@udl.cat676201743

Outcome results

None listed

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