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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

2 de noviembre de 2026 actualizado por: 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.

Descripción general del estudio

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Actual)

146

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • ICT
      • Islamabad, ICT, Pakistán, 44000
        • Shifa Tameer e Millat University

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

20 años a 60 años (Adulto)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Cuidados de apoyo
  • Asignación: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Sin intervención: 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

Experimental: 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

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
pain score
Periodo de tiempo: 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.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

15 de mayo de 2023

Finalización primaria (Actual)

29 de junio de 2023

Finalización del estudio (Actual)

30 de junio de 2023

Fechas de registro del estudio

Enviado por primera vez

28 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

2 de noviembre de 2026

Publicado por primera vez (Actual)

6 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

6 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

2 de noviembre de 2026

Última verificación

1 de mayo de 2023

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • STMU- LBP-2026-1

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Descripción del plan IPD

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

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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