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Core Strengthening Effects in Low Back Pain in Overweight Adults (CORE-BACK)

22 de julio de 2026 actualizado por: Ibadat International University, Islamabad

Effects of Core Strengthening on Mechanical Low Back Pain in Overweight Adults.

Mechanical low back pain is one of the most common musculoskeletal disorders among overweight adults and can lead to pain, disability, and reduced quality of life. Weakness of the core muscles may contribute to poor spinal stability and persistence of symptoms. Core strengthening exercises have been proposed as an effective treatment; however, evidence regarding their additional benefit over conventional physical therapy remains limited.

This randomized controlled trial aimed to determine the effects of adding core strengthening exercises to conventional physical therapy in overweight adults with mechanical low back pain. Sixty participants aged 25-45 years with a body mass index (BMI) of 25 kg/m² or greater and chronic mechanical low back pain lasting more than three months were randomly assigned to either an experimental group or a control group.

The experimental group received core strengthening exercises (planks, side planks, and superman exercises) in addition to conventional physical therapy, while the control group received conventional physical therapy alone. Both groups also received therapeutic hot packs and transcutaneous electrical nerve stimulation (TENS). Participants attended three treatment sessions per week for six weeks.

Primary outcomes included pain intensity measured by the Numeric Pain Rating Scale (NPRS), functional disability measured by the Oswestry Disability Index (ODI), and body fat percentage measured using the Jackson-Pollock skinfold method. Outcomes were assessed before and after the six-week intervention.

The study evaluated whether adding core strengthening exercises to conventional physical therapy provides greater improvements in pain, disability, and body fat percentage in overweight adults with mechanical low back pain.

Descripción general del estudio

Descripción detallada

Mechanical low back pain (MLBP) is a common musculoskeletal condition and one of the leading causes of disability worldwide. Overweight and obesity increase the mechanical load on the lumbar spine, alter spinal biomechanics, and contribute to reduced physical function and persistent pain. Excess body weight, decreased physical activity, and weakness of the trunk musculature may further compromise spinal stability, increasing the likelihood of chronic low back pain.

Core muscles, including the transversus abdominis, multifidus, erector spinae, diaphragm, pelvic floor muscles, rectus abdominis, and internal and external oblique muscles, play an essential role in maintaining spinal stability and functional movement. Strengthening these muscles may improve trunk stability, reduce mechanical stress on the lumbar spine, decrease pain, and enhance functional ability. Although several studies have investigated core stabilization exercises, evidence regarding their effectiveness in overweight adults with mechanical low back pain remains inconclusive.

This study was designed as a single-blinded randomized controlled trial to compare the effects of conventional physical therapy alone with conventional physical therapy combined with core strengthening exercises in overweight adults with chronic mechanical low back pain.

A total of 60 participants aged 25-45 years with chronic mechanical low back pain of more than three months' duration, BMI ≥25 kg/m², body fat percentage greater than 25%, and Numeric Pain Rating Scale scores below 7 were enrolled. Participants with non-mechanical low back pain, previous lumbar spine surgery, spinal fractures, spondylolisthesis, osteoporosis, neurological disorders, metabolic diseases, spinal trauma, or other serious spinal pathology were excluded.

Eligible participants were randomly allocated into two equal groups.

Experimental Group

Core strengthening exercises:

Plank Side plank Superman exercise

Conventional exercises:

Bridging Knee-to-chest exercise Back extension Pelvic rotation

Baseline physical therapy:

Therapeutic hot pack Continuous Transcutaneous Electrical Nerve Stimulation (TENS) for 10 minutes

Control Group

Conventional exercises:

Bridging Knee-to-chest exercise Back extension Pelvic rotation

Baseline physical therapy:

Therapeutic hot pack Continuous TENS for 10 minutes

Participants attended three supervised treatment sessions per week for six consecutive weeks (18 treatment sessions). Each exercise was performed for 10 repetitions with a 10-second hold and standardized rest intervals. Participants were advised to avoid heavy physical activities throughout the intervention period.

Outcome measures were assessed at baseline and after completion of the intervention. Pain intensity was evaluated using the Numeric Pain Rating Scale (NPRS). Functional disability was assessed using the Oswestry Disability Index (ODI). Body fat percentage was measured using the Jackson-Pollock three-site skinfold method.

Data analysis was performed using SPSS version 21. Normality of data distribution was assessed using the Kolmogorov-Smirnov test. Because several variables were not normally distributed, non-parametric statistical tests were used. Between-group comparisons were analyzed using the Mann-Whitney U test, while within-group pre- and post-treatment comparisons were analyzed using the Wilcoxon Signed-Rank test. Statistical significance was established at a p-value less than 0.05.

The study investigated whether the addition of core strengthening exercises to conventional physical therapy would provide greater reductions in pain intensity, disability, and body fat percentage than conventional therapy alone in overweight adults with chronic mechanical low back pain. The findings are expected to contribute to evidence-based rehabilitation strategies for managing mechanical low back pain in overweight individuals and assist clinicians in selecting effective exercise interventions for this patient population.

Tipo de estudio

Intervencionista

Inscripción (Actual)

60

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

    • Punjab Province
      • Rawalpindi, Punjab Province, Pakistán
        • Elite Physical Therapy Centre

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

  • Adulto

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

Male and female participants. Age between 25 and 45 years. Diagnosed with chronic mechanical low back pain lasting more than 3 months. Body Mass Index (BMI) ≥ 25 kg/m² (overweight or obese). Body fat percentage > 25%. Numeric Pain Rating Scale (NPRS) score < 7 at baseline. Able and willing to provide written informed consent. Willing to participate in the complete 6-week intervention program.

Exclusion Criteria:

Non-mechanical low back pain. Acute low back pain. Previous lumbar spine surgery (e.g., laminectomy or discectomy). Spondylolisthesis. Osteoporosis or spinal fractures. Cauda equina syndrome. Current history of spinal trauma or surgery. Lumbar spine myelopathy. Diagnosed metabolic diseases. Neurological disorders affecting the spine or lower limbs. Any medical condition that would contraindicate participation in the exercise program.

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: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Experimental Group (Core Strengthening + Conventional Physical Therapy)
Participants assigned to the experimental arm received a combination of core strengthening exercises (plank, side plank, and superman exercises) together with conventional physical therapy exercises (bridging, knee-to-chest, back extension, and pelvic rotation). All participants also received a therapeutic hot pack and continuous transcutaneous electrical nerve stimulation (TENS) for 10 minutes. Treatment was provided three times per week for six weeks (18 sessions).
Participants received a supervised exercise program consisting of core strengthening exercises (plank, side plank, and superman exercises) in addition to conventional physical therapy exercises (bridging, knee-to-chest, back extension, and pelvic rotation). Each exercise was performed for 10 repetitions with a 10-second hold. Participants also received a therapeutic hot pack and continuous transcutaneous electrical nerve stimulation (TENS) for 10 minutes before exercise. Treatment was provided three sessions per week for six weeks (18 sessions).
Participants received conventional physical therapy consisting of bridging, knee-to-chest, back extension, and pelvic rotation exercises. Each exercise was performed for 10 repetitions with a 10-second hold. Participants also received a therapeutic hot pack and continuous transcutaneous electrical nerve stimulation (TENS) for 10 minutes before exercise. Treatment was provided three sessions per week for six weeks (18 sessions).
Comparador activo: Control Group (Conventional Physical Therapy)
Participants assigned to the control arm received conventional physical therapy consisting of bridging, knee-to-chest, back extension, and pelvic rotation exercises. All participants also received a therapeutic hot pack and continuous transcutaneous electrical nerve stimulation (TENS) for 10 minutes. Treatment was provided three times per week for six weeks (18 sessions).
Participants received a supervised exercise program consisting of core strengthening exercises (plank, side plank, and superman exercises) in addition to conventional physical therapy exercises (bridging, knee-to-chest, back extension, and pelvic rotation). Each exercise was performed for 10 repetitions with a 10-second hold. Participants also received a therapeutic hot pack and continuous transcutaneous electrical nerve stimulation (TENS) for 10 minutes before exercise. Treatment was provided three sessions per week for six weeks (18 sessions).
Participants received conventional physical therapy consisting of bridging, knee-to-chest, back extension, and pelvic rotation exercises. Each exercise was performed for 10 repetitions with a 10-second hold. Participants also received a therapeutic hot pack and continuous transcutaneous electrical nerve stimulation (TENS) for 10 minutes before exercise. Treatment was provided three sessions per week for six weeks (18 sessions).

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Pain Intensity
Periodo de tiempo: Baseline and after 6 weeks of intervention
Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS), an 11-point scale ranging from 0 (no pain) to 10 (worst imaginable pain). Lower scores indicate reduced pain intensity.
Baseline and after 6 weeks of intervention
Functional Disability
Periodo de tiempo: Baseline and after 6 weeks of intervention
Functional disability will be measured using the Oswestry Disability Index (ODI). The ODI is a validated questionnaire that evaluates disability associated with low back pain. Lower scores indicate better functional status.
Baseline and after 6 weeks of intervention
Body Fat Percentage
Periodo de tiempo: Baseline and after 6 weeks of intervention
Body fat percentage will be measured using the Jackson-Pollock three-site skinfold method with skinfold calipers. Changes in body fat percentage will be compared before and after the intervention.
Baseline and after 6 weeks of intervention

Colaboradores e Investigadores

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

Investigadores

  • Silla de estudio: Dr Jawad Naveed, MS, Riphah College of Rehabilitation & Allied Health Sciences, Riphah International University, Islamabad

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 enero de 2023

Finalización primaria (Actual)

11 de mayo de 2023

Finalización del estudio (Actual)

30 de junio de 2023

Fechas de registro del estudio

Enviado por primera vez

10 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

22 de julio de 2026

Publicado por primera vez (Actual)

27 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

27 de julio de 2026

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

22 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

Individual participant data (IPD) collected during this study will not be shared. The informed consent obtained from participants did not include permission for public sharing of individual-level data, and no data-sharing plan was established at the time of study initiation. De-identified aggregate study results are reported in the thesis and may be made available upon reasonable request to the corresponding investigator, subject to institutional policies and ethical considerations.

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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