CClinicalTrials.gg
CompletedNCT07727525CORE-BACKUpdated Jul 27, 2026

Core Strengthening Effects in Low Back Pain in Overweight Adults

An interventional study of Core Strengthening Exercise Program + Conventional Physical Therapy and Conventional Physical Therapy in Mechanical Low Back Pain and Chronic Low Back Pain, sponsored by Ibadat International University, Islamabad. Completed at 1 site in Pakistan. Open to participants aged 25 Years to 45 Years. Per ClinicalTrials.gov, last updated 2026-07-27.

Sponsored by Ibadat International University, Islamabad · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 3 years 5 months after the study started (first participant enrolled Jan 2023, registered Jul 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
25 Years to 45 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Mechanical Low Back Pain
  • Chronic Low Back Pain

Browse trials for

Keywords

  • Mechanical Low Back Pain
  • Core Strengthening
  • Overweight Adults
  • Superman Exercise
  • Conventional Physical Therapy
03

In context

Low Back Pain

2,818 studies on the registry are indexed under Low Back Pain; 482 are open to participants now.

This study's enrollment of 60 is close to the median of 60 across 2,268 interventional studies indexed under Low Back Pain.

Browse Low Back Pain studies →

Lead sponsor

Ibadat International University, Islamabad is the lead sponsor of 49 studies on the registry; 32 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
60 participants (actual)

Study arms

  • 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).

    Procedure: Core Strengthening Exercise Program + Conventional Physical Therapy · Procedure: Conventional Physical Therapy

  • Active comparator
    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).

    Procedure: Core Strengthening Exercise Program + Conventional Physical Therapy · Procedure: Conventional Physical Therapy

Interventions

  • ProcedureCore Strengthening Exercise Program + Conventional Physical Therapy

    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).

  • ProcedureConventional Physical Therapy

    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).

06

What researchers measure

Primary outcomes

  1. Pain Intensity

    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.

    Time frame: Baseline and after 6 weeks of intervention

  2. Functional Disability

    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.

    Time frame: Baseline and after 6 weeks of intervention

  3. Body Fat Percentage

    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.

    Time frame: Baseline and after 6 weeks of intervention

07

Study locations

1 site
  • Elite Physical Therapy Centre
    Rawalpindi, Punjab Province, Pakistan
08

References and documents

Individual participant data

Plan to share: No — 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.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07727525
Lead sponsor
Ibadat International University, Islamabad
Responsible party
Sponsor
First posted
Jul 27, 2026
Start date
Jan 15, 2023
Primary completion
May 11, 2023
Completion
Jun 30, 2023
Last update
Jul 27, 2026

Study contacts

Dr Jawad Naveed, MS
study chair · Riphah College of Rehabilitation & Allied Health Sciences, Riphah International University, Islamabad

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion