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Effectiveness of a Workplace-Based Core Stability Exercise Program in Reducing Occupational Low Back Pain Among Hospital Nurses: A Quasi-Experimental Study

2026年11月2日 更新者:Huma rubab、Shifa Tameer-e-Millat University

This quasi-experimental study assessed the effectiveness of a structured, workplace-based core stability exercise program in reducing occupational low back pain (OLBP) among hospital nurses. Conducted at a tertiary care hospital in Islamabad, Pakistan, the study involved 146 registered nurses with OLBP, divided equally into an intervention group and a control group. The intervention group participated in a supervised core stability exercise regimen three times per week for four weeks, while the control group maintained routine occupational activities without structured exercise.

The core stability program emphasized neuromuscular control and strengthening of deep trunk stabilizing muscles, including the transversus abdominis, lumbar multifidus, pelvic floor muscles, diaphragm, and obliques. Each session incorporated warm-up, progressive core stability exercises, and cool-down phases, focusing on controlled movement quality over maximal effort. Exercises included abdominal drawing-in maneuvers, pelvic tilting, bridging, bird-dog, side bridge, and plank variations, with intensity progressively increased over the intervention period.

The study's rationale is grounded in Panjabi's spinal stability model, which identifies three interacting subsystems-passive (vertebrae, discs, ligaments), active (muscles, tendons), and neural control-that collectively maintain spinal stability. Occupational activities of nurses, such as manual patient handling, prolonged standing, and repetitive trunk movements, impose substantial biomechanical loads on the lumbar spine, often exceeding recommended safety limits and leading to cumulative tissue fatigue and injury. Core stability exercises target the active and neural control subsystems by enhancing deep trunk muscle activation and neuromuscular coordination, thereby improving spinal stiffness, load sharing, and movement efficiency, which collectively reduce mechanical stress on passive structures and alleviate pain.

The study's workplace-based intervention aligns with emerging evidence supporting exercise programs as effective non-pharmacological treatments for low back pain. While prior research has established core stability training benefits in chronic non-specific low back pain patients, this study addresses a gap by focusing on hospital nurses exposed to high occupational spinal loading. The pragmatic, supervised intervention demonstrated feasibility and safety, achieving full participant retention and no reported injuries.

Strengths include standardized intervention delivery, validated pain measurement, and comprehensive statistical analysis incorporating effect size estimation and sensitivity adjustment for confounders. Limitations consist of the non-randomized design, potential selection bias, imbalance in workplace department distribution, short intervention duration limiting long-term effect assessment, and reliance on self-reported pain without additional functional or biomechanical outcome measures.

Clinically, the findings advocate integrating structured core stability exercises into occupational health programs as a cost-effective strategy to mitigate OLBP, potentially reducing disability, absenteeism, and healthcare costs while enhancing nurse wellbeing and patient care quality. Future research should employ randomized controlled designs with extended follow-up and incorporate broader outcome measures such as functional capacity, muscle endurance, electromyographic activity, and quality of life to validate and extend these results.

研究概览

详细说明

The study is a quasi-experimental investigation conducted at a tertiary care hospital in Islamabad, Pakistan, aimed at evaluating the effectiveness of a structured, workplace-based core stability exercise program in reducing occupational low back pain (OLBP) among hospital nurses. A total of 146 registered nurses experiencing OLBP were enrolled and allocated into two equal groups: an intervention group (n = 73) and a control group (n = 73). Allocation was based on departmental feasibility and work schedules rather than randomization to maintain clinical workflow, reflecting a pragmatic design.

Participants in the intervention group engaged in a supervised core stability exercise program three times per week over four consecutive weeks, totaling 12 sessions. Each session lasted approximately 30-40 minutes and included three phases: a 5-10 minute warm-up with low-intensity mobility and stretching exercises targeting the lumbar spine and lower extremities; a 20-25 minute core stability training phase focusing on neuromuscular activation and strengthening of deep trunk stabilizing muscles (transversus abdominis, lumbar multifidus, pelvic floor, diaphragm, obliques, and trunk extensors) through progressive static and dynamic exercises such as abdominal drawing-in maneuvers, pelvic tilting, bridging, bird-dog, side bridge, and plank variations; and a 5-minute cool-down with gentle stretching to promote recovery. Exercise intensity was progressively increased by modifying duration, repetitions, and complexity while maintaining correct technique under physiotherapist supervision. The control group continued routine occupational activities without structured exercise.

The primary outcome was pain intensity measured by the Numeric Pain Rating Scale (NPRS), a validated 11-point scale ranging from 0 (no pain) to 10 (worst pain imaginable). Pain was assessed at baseline and immediately post-intervention. Baseline characteristics of participants, including demographic and occupational variables, were comparable between groups except for a significant difference in workplace department distribution, which was controlled for in sensitivity analyses.

Statistical analyses employed non-parametric tests due to non-normal distribution of NPRS scores. Within-group changes were analyzed using the Wilcoxon signed-rank test, and between-group differences post-intervention were evaluated using the Mann-Whitney U test. Effect sizes (r) were calculated to quantify the magnitude of changes. A sensitivity analysis using ANCOVA adjusted for baseline pain intensity and workplace department to address potential confounding from the non-randomized design.

The study's rationale is based on Panjabi's spinal stability model, which describes spinal stability as a function of the passive (vertebrae, discs, ligaments), active (muscles, tendons), and neural control subsystems. Occupational activities of nurses, including manual patient handling and prolonged static postures, impose repetitive biomechanical loading on the lumbar spine, risking tissue fatigue and injury. Core stability exercises target the active and neural subsystems by enhancing deep trunk muscle activation and neuromuscular coordination, improving spinal stiffness, load sharing, and movement efficiency, thereby reducing mechanical stress on passive structures and alleviating pain.

Strengths of the study include standardized, supervised intervention delivery, 100% participant retention, validated pain measurement, and comprehensive statistical analysis with effect size reporting and sensitivity adjustment. Limitations include the quasi-experimental non-randomized design with potential selection bias, imbalance in workplace department distribution, short intervention duration limiting assessment of long-term effects, and reliance solely on self-reported pain without functional or biomechanical outcome measures.

The study was approved by the Institutional Review Board and Ethics Committee of Shifa International Hospitals, Islamabad, Pakistan, and conducted in accordance with the Declaration of Helsinki. Written informed consent was obtained from all participants. No external funding was received, and the authors declared no conflicts of interest.

研究类型

介入性

注册 (实际的)

146

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • ICT
      • Islamabad、ICT、巴基斯坦、44000
        • Shifa Tameer e Millat University

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

20年 至 60年 (成人)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Eligible participants were registered nurses who met the following inclusion criteria:

    • aged between 20 and 60 years;
    • employed as full-time nursing staff;
    • had experienced occupational low back pain for at least three months;
    • reported a pain intensity of 3 or greater on the Numerical Rating Scale (NRS);
    • were able to participate safely in light-to-moderate physical exercise; and
    • provided written informed consent before participation.

Exclusion Criteria:

Participants were excluded if they:

  • had undergone spinal surgery within the previous year;
  • had a history of spinal fracture, malignancy, inflammatory spinal disease, or severe neurological disorders;
  • were pregnant;
  • had acute traumatic musculoskeletal injuries;
  • were currently participating in another structured rehabilitation or exercise program targeting low back pain; or
  • had any medical condition that contraindicated participation in therapeutic exercise.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:非随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
无干预:Control Group

The control group in this quasi-experimental study consisted of 73 registered nurses who continued their routine occupational activities without participating in any structured exercise program targeting low back pain. Throughout the four-week study period, these participants maintained their usual work duties in the hospital setting without receiving any supervised core stability exercises or other intervention. They were specifically instructed not to engage in any additional structured exercise programs aimed at managing low back pain during the intervention period.

Pain intensity in the control group was measured at baseline and immediately post-intervention using the Numeric Pain Rating Scale (NPRS). The control group showed minimal change in pain intensity over the study period, with median NPRS scores remaining largely unchanged (from 4 at baseline to 4 post-intervention). No adverse events or injuries were reported.

The control group's role was to serve as a comparator to asse

实验性的:Structured Workplace-Based Core Stability Exercise Program

The intervention consisted of a structured, workplace-based core stability exercise program aimed at improving neuromuscular control of the lumbopelvic region, enhancing spinal stability, and reducing occupational low back pain among hospital nurses. Participants in the intervention group undertook this supervised exercise regimen three times per week for four consecutive weeks, totaling 12 sessions. Each session lasted approximately 30 to 40 minutes and was overseen by a trained physiotherapist to ensure correct technique, safety, and adherence.

Each session comprised three phases:

  1. Warm-up (5-10 minutes):

    Low-intensity mobility and stretching exercises targeting the lumbar spine, pelvis, and lower extremities were performed to increase muscle temperature, improve joint mobility, and prepare the neuromuscular system for the core exercises.

  2. Core Stability Training (20-25 minutes):

This phase focused on activating and strengthening the deep trunk stabilizing muscles, including the

This intervention is distinguished from other clinical studies by several key features based on the provided document:

  1. Workplace-Based and Pragmatic Design:

    The core stability exercise program was implemented directly within the hospital workplace environment, specifically tailored to the clinical setting of hospital nurses in a tertiary care hospital in Islamabad, Pakistan. Unlike many interventions conducted in controlled or outpatient rehabilitation settings, this program was integrated into the nurses' routine work schedules, enhancing ecological validity and feasibility.

  2. Non-Randomized, Department-Based Allocation Reflecting Real-World Constraints:

Participants were allocated based on departmental feasibility and work schedules rather than randomization, preserving clinical workflow and minimizing disruption to patient care. This pragmatic approach reflects real-world occupational health program implementation challenges, distinguishing it from more controlled randomized tri

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
pain score
大体时间:Baseline (prior to the intervention) Five weeks post-baseline, corresponding to one week after completion of the four-week intervention period.

Pain intensity was measured using the Numeric Pain Rating Scale (NPRS), an 11-point validated and reliable patient-reported measure ranging from 0 ("no pain") to 10 ("worst pain imaginable"). Participants rated the average intensity of their occupational low back pain experienced during routine work activities. Pain assessments were conducted at two specific time points: baseline (prior to the intervention) and at five weeks post-baseline, which corresponds to one week after completing the four-week intervention period.

Baseline (prior to the intervention) Five weeks post-baseline, corresponding to one week after completion of the four-week intervention period.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2023年5月15日

初级完成 (实际的)

2023年6月29日

研究完成 (实际的)

2023年6月30日

研究注册日期

首次提交

2026年10月28日

首先提交符合 QC 标准的

2026年11月2日

首次发布 (实际的)

2026年11月6日

研究记录更新

最后更新发布 (实际的)

2026年11月6日

上次提交的符合 QC 标准的更新

2026年11月2日

最后验证

2023年5月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

IPD 计划说明

this was not consented thats why we can relook by approaching to the participants

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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