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A study to investigate the effects of an exercise program focusing on core body muscles in patients with low back pain after a C-section

Effects of supervised versus unsupervised home-based core stability exercise programs in post C-section low back pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN12478688
Enrollment
30
Registered
2018-07-31
Start date
2018-08-01
Completion date
Unknown
Last updated
2020-01-06

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

Conditions

Post C-section low back pain Musculoskeletal Diseases Low back pain

Interventions

Informed consent will be taken from all the study participants. The participants will then be asked to complete Oswestry Disability Index and a questionnaire of open-ended questions. 40 participants w
however, group I will be treated with a supervised version, whereas group II will be provided with an unsupervised, home-based core stability exercise program. Both the supervised and unsupervised pro

Sponsors

Riphah International University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Post C-section low back pain for a minimum of 2 months and maximum of 2 years 2. Aged 25-40 years

Exclusion criteria

Exclusion criteria: Participants with other systemic, bone and soft tissue diseases including: 1. Lumbar spinal stenosis 2. Spondylosis 3. Spondylolisthesis 4. Lumbar radiculopathy 5. Spinal cord injury 6. Paraplegia 7. Fractures 8. Herniated lumbar disc 9. Scheuermann’s disease 10. Ankylosing spondylitis 11. Rheumatoid arthritis 12. Osteoporosis etc.

Design outcomes

Primary

MeasureTime frame
The following were assessed at the baseline and 6 weeks (end of the intervention): 1. Low back pain measured using Oswestry Disability Index (ODI) and Numeric Pain Rating Scale (NPRS) 2. Core stability assessed using the Core Stability Assessment Scale

Secondary

MeasureTime frame
Current secondary outcome measures as of 26/09/2018: Range of motion, assessed using an incliometer at the baseline and 6 weeks (end of the intervention) Previous secondary outcome measures: Goniometry of lumbar spine, assessed using goniometer at the baseline and 6 weeks (end of the intervention)

Countries

Pakistan

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 16, 2026