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临床试验/NCT07799415
NCT07799415已完成不适用

Effect of Exercise Intervention on Pain, Disability, Job Stress, and Quality of Life in Office Workers With Neck Pain

Sumaya Sadıgova1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年12月29日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
Neck Disability Level

研究概览

简要总结

This clinical trial aims to learn if a structured exercise intervention helps treat chronic neck pain, reduce neck disability, relieve work-related stress, and improve overall quality of life in office workers.

The main questions it aims to answer are:

Does a targeted exercise intervention significantly reduce neck pain intensity and neck disability in office workers?

Does the exercise program help lower work-related stress levels among office employees?

Does the intervention provide significant improvements in the health-related quality of life of the participants?

Participants will:

Complete a baseline assessment evaluating their current neck pain, functional disability, work-related stress levels, and quality of life using validated clinical questionnaires and measurements.

Engage in a structured exercise program focused on deep neck flexor strengthening, upper back/shoulder strengthening, muscle stretching, and postural alignment.

Complete a post-intervention evaluation immediately following the completion of the exercise program to measure changes in pain, disability, stress, and quality of life.

详细描述

1. INTRODUCTION

With the digitalization of working life, the center of gravity of work-related musculoskeletal disorders has shifted from occupational sectors dominated by heavy physical loads to office environments characterized by prolonged static loads. The office worker spends the majority of the day in a sitting position, with the head and neck fixed toward the screen and the upper extremities relatively immobile over the keyboard and mouse. When considered individually, this working pattern appears harmless; however, it creates a cumulative mechanical and neuromuscular load on the cervical region, with neck pain emerging as the most visible clinical outcome.

Neck pain ranks among the top contributors to years lived with disability worldwide among musculoskeletal conditions. Global Burden of Disease data show that neck pain is a widespread and persistent public health burden, and this burden will continue to rise as working patterns become increasingly digitalized. A problem so prevalent in the general population becomes even more pronounced in groups with concentrated exposure, such as office workers, where the annual prevalence of neck pain in this population is reported to range between 42% and 63%. Research conducted on computer-using office workers in Turkey also confirms that the most frequently reported musculoskeletal symptom occurs in the neck region.

The vast majority of neck pain observed in office workers is non-specific in nature; meaning no specific identifiable structural pathology can be shown as the source of pain. Nevertheless, the pain significantly impacts the individual's daily living activities, work performance, and psychological well-being. A cluster of interacting mechanisms plays a role in its pathogenesis. Under prolonged static posture, activation of the deep cervical flexor muscles decreases, while compensatory hyperactivation develops in the superficial muscles. This neuromuscular reorganization weakens the dynamic support of the cervical segments, impairs proprioceptive feedback, and creates a vicious cycle that contributes to the persistence of pain. Viewing the issue solely through a biomechanical lens provides an incomplete framework; evidence is growing stronger that psychosocial factors-such as job stress, low job satisfaction, and lack of support-play a decisive role in the onset and chronicity of neck pain.

In the management of non-specific neck pain, exercise currently holds the strongest evidence base among intervention methods. Strengthening, stretching, and motor control exercises targeted at the cervical and scapulothoracic regions have been shown to exert positive effects on pain, disability, and quality of life, while also improving psychosocial outcome measures such as job stress.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

盲法说明

No masking is used in this study. The study is an open-label trial where all participants and researchers are aware of the group assignments.

入排标准

年龄范围
25 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women aged 25 to 60 years
  • Currently employed as office workers with continuous computer usage
  • Ability to participate in and adhere to the intervention protocol
  • Diagnosis of chronic non-specific neck pain lasting for more than 3 months

排除标准

  • Previous history of physical therapy or rehabilitation for neck pain
  • History of cervical spine surgery
  • Cervical joint instability
  • Diagnosis of migraine or other severe headache disorders
  • Spasmodic torticollis
  • Inflammatory rheumatic diseases (e.g., rheumatoid arthritis, ankylosing spondylitis)
  • Peripheral nerve entrapment syndromes (e.g., cervical radiculopathy, carpal tunnel syndrome)
  • Presence of severe psychiatric disorders

研究组 & 干预措施

Physiotherapist-Supervised Exercise Group

Experimental

Participants in this arm receive a 6-week structured progressive exercise program delivered under the direct, face-to-face supervision of a qualified physiotherapist. The intervention consists of 18 clinical sessions (3 sessions/week, 45 minutes/session). The exercise protocol is divided into three 2-week phases: Phase 1 focuses on deep cervical flexor re-education (longus colli/capitis) using tactile feedback, along with stretching hypertonic upper trapezius and levator scapulae muscles; Phase 2 incorporates elastic band (TheraBand) progressive resistance training targeting the lower/middle trapezius and serratus anterior, alongside seated isometric neck stabilization; Phase 3 emphasizes cervicothoracic dynamic endurance, active range of motion, and postural integration. The physiotherapist provides continuous real-time movement correction, regulates resistance progression, and monitors adverse symptoms during every session.

干预措施: Supervised Therapeutic Exercise Program, Control Grupu (Behavioral)

Control Group

Active Comparator

Participants in this arm perform an identical 6-week progressive exercise protocol in terms of content, volume, and phased progression; however, the intervention is entirely self-directed without physical physiotherapist presence. Participants access high-definition instructional video demonstrations, movement safety guides, and exercise parameters (sets, reps, hold times) via a dedicated mobile application. The schedule mirrors Arm 1 (3 sessions/week, 40-45 minutes/session for 6 weeks). The mobile platform automatically unlocks Phase 1 (deep flexor activation and stretching), Phase 2 (scapular band exercises), and Phase 3 (dynamic endurance and mobility) every two weeks. Automated app notifications remind participants to complete scheduled sessions, and adherence is logged digitally within the application.

干预措施: Supervised Therapeutic Exercise Program, Control Grupu (Behavioral)

结局指标

主要结局

Neck Disability Level

时间窗: Baseline and Week 6 (immediately after the 6-week intervention)

Change in Neck Disability Level

次要结局

未报告次要终点

研究者

发起方
Sumaya Sadıgova
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Sumaya Sadıgova

Master Student, Department of Physiotherapy and Rehabilitation

Istanbul University - Cerrahpasa

研究点 (1)

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