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Pilates Exercises on Nonspecific Low Back Pain in Postnatal Women

The Effect of Pilates Exercises on Nonspecific Low Back Pain in Postnatal Women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07359144
Enrollment
48
Registered
2026-01-22
Start date
2026-01-22
Completion date
2026-07-01
Last updated
2026-01-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain, Nonspecific, Pilates Exercises, Postnatal Women

Brief summary

This study aims to investigate the effects of Pilates for postnatal women with Non-specific low back pain (NSLBP).

Detailed description

Low back pain (LBP) is of high prevalence among adults, which can be related to factors such as sedentary lifestyle, being overweight or work conditions. Non-specific LBP (NSLBP) is defined as pain in the lower back region that cannot be attributed to a recognizable, specific pathology such as infection, fracture, or nerve root compression. Pilates exercises focus on improving core stability, flexibility, posture, and body awareness through controlled, precise movements. The integration of breathing techniques and concentration enhances the mind-body connection, which can contribute to pain reduction and functional improvement. For individuals with LBP, Pilates has been shown to improve strength and flexibility, reduce pain intensity, and enhance overall physical function, making it a promising intervention for managing musculoskeletal disorders.

Interventions

OTHERPilates program + Home exercise program

Patients will do a comprehensive exercise consisting of a home exercise program (bridges, bridge with leg extension (bridge dog), back extensions, spine twist, and child's pose), a Pilates program, and oral paracetamol as needed for pain relief.

OTHERHome exercise program

Patients will perform a home-based exercise program consisting solely of postural correction exercises.

Sponsors

Kafrelsheikh University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

* Age ranges from 20 and 30 years old. * Body mass index (BMI) doesn't exceed 30 kg/m2. * Patients who are referred from a gynecologist with a diagnosis of nonspecific low back pain. * Patients who have pain for more than three months. * Patients who have parity ranging from one to three (to control the extreme physiological changes from multiple childbirths, ensuring a more uniform sample). * Patients who have score more than 4 on the Visual Analog Scale (VAS).

Exclusion criteria

* Mechanical low back pain (LBP). * Women who had performed any spinal surgery e.g. unilateral hemilaminectomy or microdiscectomy. * Women with history of vertebral fracture or trauma. * Women with systemic disorder e.g. diabetes mellitus. * Women who are pregnant. * Women who had received physiotherapy treatment for their LBP one month before the start of this study.

Design outcomes

Primary

MeasureTime frameDescription
Pain Intensity3 months post-procedurePain Intensity will be assessed using Visual Analog Scale (VAS). VAS (0 represents "no pain" while 10 represents "the worst pain imaginable").

Secondary

MeasureTime frameDescription
Assessment of pain pressure threshold3 months post-procedurePain pressure threshold (PPT) will be determined using a handheld electronic pressure algometer with a 1 cm2 probe area with an increasing of the pressure rate of 20 Kpa/s. The pressure algometer consists of a "pistol" handle and a rod with a pressure-sensitive gauge strain at the tip.
Assessment of functional disability3 months post-procedureOswestry Disability Index will be used to assess functional disability. It is a self-assessing questionnaire for low back pain, which includes 10 items; each contains six levels of answers ranging from 0-5. Its items include pain intensity, personal care, lifting objects, walking, sitting, standing, sleeping, sex life, social life, and travelling. A total score is calculated, divided by 50, and multiplied by 100. It ranges from 0% indicating no disability to 100% indicating complete disability.
Assessment of the quality of life3 months post-procedureQuality of life (QOL) will be assessed using SF-36 Questionnaire. SF-36 questionnaire consists of thirty-six questions measuring PH components (physical function, role physic, bodily pain, general health and MH components (vitality, social functioning, role emotion, general mental health). The response for each item was scored from 0-100, and the mean score of each domain was calculated. Lower score implied poor QoL, whereas higher score indicated excellent QoL.

Countries

Egypt

Contacts

CONTACTEman M Elsheikh, MBBCH
emanelshiekh858@gmail.com00201009094244

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026