Lumber Stabilization Exercise Versus Back Endurance Exercise Among Female University Students
RecruitingNot applicableNCT07163117
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
Low Back Pain (LBP) as estimates show that up to 84% of adults will experience LBP at some point in their lifetime, ranking it as a leading cause of disability globally. If the pain lasts more than 12 weeks and remains difficult to manage effectively, it can be called Chronic low back pain (CLBP). Physical therapy interventions play an important role in the non-pharmacological management of CLBP including lumbar stabilization exercises (LSEs) and back extension/endurance exercises which are commonly prescribed modalities that may help in improving the spinal function, reducing pain and improving the quality of life in general.
Study details
- Official title
- The Efficacy of Lumber Stabilization Exercise Versus Back Endurance Exercise on the Range of Motion of the Lumber Spine and Its Stability Among Female University Students
- Conditions
- Interventions
- Other: lumbar stabilization exercises
- Other: endurance training
- Other: Home based program
- Sponsor
- Cairo University
- Start date
- 2025-09-09
- Primary completion
- 2025-12-15
- Sex
- Female
- Age range
- from 18 Years to 24 Years
- Results posted
- No results posted in this snapshot
- Countries
- Egypt
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * BMI ranged from 28 to 29 kg/ cm2. * clinically diagnosed by an orthopedic consultant as having a history of mechanical low back pain for at least three months. Exclusion Criteria: * Previous trauma. * Previous surgery. * Any musculoskeletal disorder * Any neurological disorder (disc prolapse, or spondylosis)
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07163117