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Effect of Core Stability and Treadmill Walk Exercises on the Functional Status of Post Lumbar -Surgical Patients With Low Back Pain: A Randomised Cont

Effect of Core Stability and Treadmill Walk Exercises on the Functional Status of Post Lumbar -Surgical Patients With Low Back Pain: A Randomised Control Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201710002646362
Enrollment
80
Registered
2017-09-26
Start date
2018-01-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Musculoskeletal Diseases Surgery POST-SURGICAL LOW BACK PAIN

Interventions

GROUP A
GROUP B
GROUP C
GROUP D

Sponsors

FARIDA GARBA SUMAILA
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Participants for this study will be at least 18 years old, had undergone spinal surgery and a history of chronic and/or recurrent LBP (repeated episodes of pain in past year collectively lasting for more than 3 months), with or without leg pain, and is presenting with recurrent LBP. They should be able to read/understand English and/or Hausa languages. Participants should be at Phase IV which is the Recovery phase (20 weeks to 1 year post-surgery) according to the Recommendations for the rehabilitation of post-surgical spinal patients by Maxey and Magnusson (2001).

Exclusion criteria

Exclusion criteria: Participants with low back pain caused by red flag factors (such as cancer, tuberculosis, tumour and other serious spinal pathological conditions as outlined in the Clinical Standards Advisory Group (CSAG) report for back pain (CSAG 1994) and also those patients with any organic pathology like spinal cord injury, systemic inflammatory diseases, disc prolapse, radiculopathy, inflammatory arthritis, pregnancy related, fractures, infections osteoporosis, spondylolisthesis, spinal stenosis and morbid obesity, uncontrolled diabetes and uncontrolled hypertension or heart problems will be excluded from the study. Participants will also be excluded from the study if they have one or more of the following criteria: pregnancy; significant physical or mental deficiencies preventing a clear understanding of the clinical trial procedure.

Design outcomes

Primary

MeasureTime frame
Pain;Functional Disability;Quality of Life

Countries

Nigeria

Contacts

Public ContactFARIDA GARBA SUMAILA

LECTURER I

fareedat2006@gmail.com+234 80 3616 4228

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026