Effects Of 8-Week Core Stabilization Exercise With Vitamin D On Pain and Functional Limitation in Adults
Active, not recruitingNot applicableNCT06913413
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
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)
Chronic non-specific low back pain (CNSLBP) is a prevalent condition contributing to pain, functional limitations, and reduced quality of life. Core stabilization exercises (CSE) have shown promise in enhancing spinal stability and reducing symptoms. Additionally, vitamin D supplementation plays a critical role in musculoskeletal health. Study objective will be to determine combined effect of vitamin D supplementation and core Stabilization exercises is better than core Stabilization Exercises alone in reducing pain-related and functional independence among chronic non-specific low back patient A randomized controlled trial will be conducted on 52 adults aged 25-45 diagnosed with Chronic non-specific low back pain.
Study details
- Official title
- Effects Of 8-Week Core Stabilization Exercise With Vitamin D On Pain and Functional Limitation in Adults With Chronic Non-Specific Low Back Pain
- Conditions
- Interventions
- Combination product: core stabilization exercise
- Diagnostic test: stabilization exercise
- Sponsor
- Superior University
- Start date
- 2025-03-20
- Primary completion
- 2025-06-20
- Sex
- All
- Age range
- from 25 Years to 40 Years
- Results posted
- No results posted in this snapshot
- Countries
- Pakistan
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Adults aged 25 to 45 years will be included. * Both gender Male /Female will participate. * Subjects with diagnosed non-specific low lumber pain persisting for at least 12 weeks will be included. * Subjects must have baseline pain score of ≥4 on the Visual Analog Scale. * Confirmed serum vitamin D levels \<30 ng/m will be included Exclusion Criteria: * Low lumber pain due to specific causes such as fracture malignancy infection or inflammatory diseases (e.g. ankylosing spondylitis). * Presence of significant comorbidities that could interfere with participation (e.g. cardiovascular neurological or respiratory disorders). * History of spinal surgery within the last year. * Subjects currently taking vitamin D supplements or undergoing other treatments for vitamin D deficiency. * Use of medications such as corticosteroids or opioids that might affect pain perception or functional assessment. * Enrolled in any other physical therapy or pain management program within the last three months.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06913413