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Neck Pain in Office Workers

1 mai 2026 mis à jour par: Vilma Dudoniene, Lithuanian Sports University

Effect Of Short Neck-Stretching Exercise Breaks On Neck Pain And Related Factors In Office Workers

The aim of this study is to evaluate effectiveness of short exercise breaks (2, 5, and 7 minutes) on chronic non-specific neck pain in office workers. It is a 12-week randomized controlled trial assessing pain, disability, and multiple functional and occupational outcomes. We aim to determine the most effective exercise duration for reducing neck pain and improving quality of life, productivity, and job satisfaction.

Aperçu de l'étude

Statut

Inscription sur invitation

Les conditions

Description détaillée

This study investigates the effectiveness of brief exercise breaks of different durations (2, 5, and 7 minutes) in managing chronic non-specific neck pain among office workers. Neck pain is highly prevalent in individuals exposed to prolonged computer use and static postures, and it is associated with reduced quality of life, decreased work productivity, and increased occupational strain. Although exercise-based interventions are recommended, adherence to traditional home programs remains low, highlighting the need for simple and time-efficient strategies.

The study was designed as a 12-week, double-blind, randomized controlled trial. Participants with chronic non-specific neck pain and are randomly assigned to one of three intervention groups (2-, 5-, or 7-minute exercise programs) or a control group. We plan to enroll at least 120 participants.

Type d'étude

Interventionnel

Inscription (Estimé)

120

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Lt-44221
      • Kaunas, Lt-44221, Lituanie, 44221
        • Department of health promotion and rehabilitation

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Office workers engaged in sedentary work for at least 6 hours per day.

Exclusion Criteria:

  • individuals with a specific neck diagnosis or acute neck pain.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Tripler

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: 2 min exercise
Participants of this arm have uing work hours to complete 2 min exercise programme each hour
Participants are required to perform the exercises during working hours, once every hour throughout the workday.
Comparateur actif: 5 min exercise
Participants of this arm have uing work hours to complete 5 min exercise programme each hour
Participants in this group are required to perform the 5 min duration exercises during working hours, once every hour throughout the workday.
Comparateur actif: 7 min exercise
Participants in this group are required to perform the 7 min duration exercises during working hours, once every hour throughout the workday.
Participants in this group are required to perform the 7 minn duration exercises during working hours, once every hour throughout the workday.
Aucune intervention: Controls
participants of this group will not get any intervention

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Neck Disability Index
Délai: Pre-post intervention (12 week)
The questionnaire consists of 10 items, each scored from 0 to 5. The total score is interpreted as a percentage, where 0 points or 0% indicates no ac-tivity limitation, and 50 points or 100% indicates complete activity limitation. The NDI is a reliable and valid tool for assessing patients with neck pain, with intraclass correlation coefficients ranging from 0.50 to 0.98. Patients scoring between 0-4 points (0-8%) are considered to have no disability, 5-14 points (10-28%) mild disability, 15-24 points (30-48%) moderate disability, 25-34 points (50-64%) severe disability, and 35-50 points (70-100%) complete disability
Pre-post intervention (12 week)
Postural stability
Délai: Pre-post intervention (12 week)
Postural stability is assessed using the Biodex Balance System (BBS; Biodex Medical Systems Inc., Shirley, NY, USA), a validated computerized platform widely used to quantify balance performance and neuromuscular control in both healthy and clinical populations. Participants stood barefoot on the dynamic platform, with foot placement standardized by the system to ensure consistency across trials. They were instructed to maintain an upright posture with hands on the hips and to focus on a monitor positioned in front of them, which provided real-time visual feedback, enabling continuous monitoring and voluntary correction of postural sway (Biodex Medical Systems, 2020).Outcome measures automatically recorded by the BBS included the Overall Stability Index), Anterior-Posterior Stability Index, Medial-Lateral Stability Index, Overall Sway Index, Anterior-Posterior Sway Index, Medial-Lateral Sway Index, and Time-in-Zones percentages.
Pre-post intervention (12 week)
Bilateral Coordination
Délai: Pre-post (12 wek)

Bilateral coordination are assessed using the Bilateral Comparison Test module of the Biodex Balance System (BBS), which evaluates static postural sway and interlimb symmetry under controlled conditions [24, 25]. Participants performed a single trial consisting of a 10-second single-leg stance on the left leg followed immediately by a 10-second single-leg stance on the right leg. All trials were conducted barefoot, with hands placed on the hips, while the platform remained static to isolate static balance control.

The BBS automatically generate the following outcome measures: Overall Left and Right Sway Indices, Overall Interlimb Difference, Anterior-Posterior (A/P) Left and Right Sway Indices, A/P Interlimb Difference, and Medial-Lateral (M/L) Left and Right Sway Indices, as well as M/L Interlimb Difference (Supplementary Figure 2).

Lower sway index values indicate better postural stability, reflecting reduced body sway. Smaller interlimb differences indicate greater bilateral symme

Pre-post (12 wek)
Manual dexterity performance (Purdue Pegboard Test)
Délai: Pre-post (12 week)
The Purdue Pegboard Test Model #32020A was used to assess unimanual and bimanual finger and hand dexterity performance among office workers with neck pain. This test was recognized as a reliable and valid tool for fine motor skills assessment and can be used for assessment in case of a variety of neurological disorders. The three test batteries were performed: 1) dominant hand; 2) non dominant hand; 3) both hands. The test procedures were performed according to the Purdue Pegboard Test User Instructions. The board was placed on a table in front of the subject comfortably sitting on a chair. The top right and left cups were filled with 25 pins in each to equal a total of 50 pins. Before performing the test the subject was instructed: "This is a test to see how quickly and accurately you can work with your hands. Before you begin each battery of the test, you will be told what to do and then you will have an opportunity to practice. Be sure you understand exactly what to do.
Pre-post (12 week)
Miotonometry
Délai: Pre-post (12 week)
Muscle tone was assessed using a myotonometer. The tone of the upper trapezius muscle was measured with a Myoton PRO device (Myoton AS, Tallinn, Estonia). This method allows for a simple and noninvasive evaluation of the mechanical properties of muscles and demonstrates high reliability, with an intra-rater correlation coefficient ranging from 0.94 to 0.99. Participants were seated on a chair with back support with both hands resting on their thighs and looked straight ahead during the measurements. Measurements were performed on the upper trapezius muscle bilaterally (right and left) at the midpoint of the line connecting the spinous process of the C7 vertebra and the acromion of the scapula. Three biomechanical parameters were recorded: muscle tone (Hz), elasticity (logarithmic decrement), and stiffness (N/m). During the measurement, the skin was preloaded with a force of 0.18 N, followed by five mechanical impulses of 0.4 N applied at 15-second interval
Pre-post (12 week)
Neck pain
Délai: pre and post intervention (12 week)

Numeric pain scale. Participants rate their pain on a scale from 0 to 10, where:

0 = no pain,10 = worst imaginable pain

pre and post intervention (12 week)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Age
Délai: Once- pre intervention
in years
Once- pre intervention
Body Composition
Délai: Pre-post (12 week)
Body height was measured using a wall-mounted stadiometer equipped with a centimeter scale. Body composition was assessed using a bioelectrical impedance analyzer (TANITA BC 240 SMA, Tanita, Tokyo, Japan). The body composition parameters evaluated in this study included fat mass (kg and %), fat-free mass (kg and %), and muscle mass (kg and %).
Pre-post (12 week)
Sleep Quality (Numeric Scale)
Délai: pre-post (12 week)

Sleep quality was assessed using a numeric rating scale. Participants rated their overall sleep quality on a scale from 0 to 10, where 0 indicated very poor sleep and 10 indicated excellent sleep. Higher scores reflect better perceived sleep quality.

The SQS is a self-administered questionnaire that incorporates a discretizing VAS. The questionnaire instructions direct the respondent to rate the overall quality of sleep over a 7-day recall period on a discretizing VAS, whereby the respondent marks an integer score from 0 to 10, according to the following five categories: 0 = terrible, 1-3 = poor, 4-6 = fair, 7-9 = good, and 10 = excellent

pre-post (12 week)
Minnesota Satisfaction Questionnaire
Délai: Pre-post (12 week)
The MSQ-Short Form consists of 20 items assessing intrinsic (12 items) and extrinsic (8 items) job satisfaction. Items are rated on a 5-point Likert scale from 1 (very dissatisfied) to 5 (very satisfied). The global satisfaction score is calculated by averaging all item scores. The neutral score is 3; scores above 3 indicate high job satisfaction, while scores below 3 indicate low job satisfaction. The maximum total score is 100, representing the highest possible job satisfaction.
Pre-post (12 week)
Hand Grip Strength
Délai: Pre-post (12 week)
Grip strength was measured using a Saehan SH5001 hand dynamometer (Germany). Measurements for both the dominant and non-dominant hands were taken. The maximum grip strength was recorded in kilograms (kg). Three measurements were taken with 15 seconds of rest between each trial, and the average result was recorded
Pre-post (12 week)
Short Form-36 Health Surve
Délai: Pr-post (12 week)
is a widely used patient-reported questionnaire designed to assess health-related quality of life (HRQoL) in both clinical and general populations. It consists of 36 items covering eight health domains: Physical functioning Role limitations due to physical health Bodily pain General health perceptions Vitality (energy/fatigue) Social functioning Role limitations due to emotional problems Mental health Each domain is scored on a scale from 0 to 100, where higher scores indicate better health status and functioning. The SF-36 provides two summary measures: the Physical Component Summary (PCS) and the Mental Component Summary (MCS).
Pr-post (12 week)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

1 août 2025

Achèvement primaire (Estimé)

1 août 2027

Achèvement de l'étude (Estimé)

1 août 2027

Dates d'inscription aux études

Première soumission

24 avril 2026

Première soumission répondant aux critères de contrôle qualité

24 avril 2026

Première publication (Réel)

1 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

7 mai 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

1 mai 2026

Dernière vérification

1 avril 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

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INDÉCIS

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

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