- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06914271
Effects of Kendall Exercises Versus Kabat Exercises in Patients With Chronic Low Back Pain
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab
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Sialkot, Punjab, Pakistan
- Younas hospital daska
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Both Genders
- Adults Aged Between 30-65
- Low Back pain should be Persistent for more than 12 weeks
- Visual Analogue scale or VAS of 3 or higher
- Idiopathic pain
- Ability to engage in physical activity and participate in the intervention program
- Willingness and ability to provide informed consent to participate in the study
Exclusion Criteria:
Low back pain due to other causes
- Fibromyalgia
- Previous spine surgery
- Spondylolisthesis
- Spondylolysis
- Rheumatoid arthritis or Ankylosing spondylitis
- Spinal inflammation or tumor
- Spinal or pelvis fracture
- Osteoporosis
- Respiratory or heart diseases
- Stroke
- Pregnancy
- Persistent use of pain medication
- Patients who had undergone any other treatments, such as acupuncture or physical therapy, in the last 3 months
- Anticipated inability to comply with study protocols or attend scheduled."
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Kendall Exercise
|
The Kendall Exercises focus on correcting posture, strengthening the core, and re-educating muscles to improve spinal alignment and reduce pain .These exercises primarily target specific muscles and joint actions to help patients regain their range of motion.
|
|
Active Comparator: Kabat Exercises
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The principle of the Kabat exercises is based on a series of neuromuscular facilitation techniques that emphasize dynamic movement patterns, flexibility, and coordination to enhance functional mobility and alleviate pain.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analogue Scale
Time Frame: 12 Months
|
The Visual Analogue Scale (VAS) is a way of measuring pain intensity.
It is often utilized in investigations concerning pain management.
Visual analog scales (VAS) are psychometric measuring tools created to record the characteristics of disease-related symptom severity in individual patients and utilize this to achieve a quick (statistically observable and reproducible) classification of symptom severity and disease control.
Scores are taken by placing a handwritten mark along a 10-cm line that depicts a pain spectrum between ""no pain"" and ""worst pain.""
|
12 Months
|
|
Oswestry Disability Index (ODI)
Time Frame: 12 Months
|
The Oswestry Disability Index (ODI) is a widely used instrument for determining the degree of impairment and how low back pain affects a person's ability to do daily chores. Each of its 10 sections focuses on a different aspect of everyday life, such as pain severity, personal cleanliness, walking, lifting, sitting, standing, sleeping, and social life. A person's scores for each component are added based on the severity of their condition to determine their total disability percentage, which can range from 0% (no impairment) to 100% (severe disability). It is widely used in clinical settings to track changes over time and assess the effectiveness of treatments for low back pain (27). The Oswestry Disability Index (ODI) exhibits great validity (correlation with VAS: r= 0.67; Roland Morris: r=0.76) and high reliability (Cronbach's α > 0.70, ICC > 0.90) |
12 Months
|
|
Goniometer
Time Frame: 12 Months
|
A Goniometer is simple yet effective tool used to measure the range of motion of a joint. 0% to 20%: minimal disability: 21%-40%: moderate disability: 41%-60%: severe disability: Pain remains the main problem in this group but activities of daily living are affected. These patients require a detailed investigation. 61%-80%: crippled: Back pain impinges on all aspects of the patient's life. Positive intervention is required. 81%-100%: These patients are either bed-bound or exaggerating their symptoms. |
12 Months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MSRSW/Batch-Fall23/819
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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