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Clinical Trials/NCT06399549
NCT06399549
Active, not recruiting
Not Applicable

Effects of Dead Bug vs. Mc Gill Exercises on Pain, Quality of Life and Core Stability in Patient With Chronic Nonspecific Low Back Pain

Superior University1 site in 1 country44 target enrollmentMarch 9, 2024
ConditionsLow Back Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
Superior University
Enrollment
44
Locations
1
Primary Endpoint
VA
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

Low back pain is one of the most common conditions for which patients are sent to physiotherapy clinics. 84% of people have experienced it at least once in their lifetime, and over 50% have experienced it more than once, according to research. However, diagnosis and, in particular, the provision of specialized back pain therapy remain difficult.

Detailed Description

This study aims to compare the effects of dead bug vs. Mc Gill exercises on pain, quality of life and core stability in patient with chronic nonspecific low back pain. It will be a randomized clinical trial study. The sample size of study will be 44 participants (22 in each group). Data will be collected from Azra Naheed Hospital. Data will be collected within 6 months after approval of synopsis. Group A will follow dead bug exercises and Group B will follow Mc Gill exercises (Curl up, Side Bridge and Bird Dog). The patients in both groups will be performed the corresponding exercises 3 days a week and 10 repetitions of each exercise for a period of 6 weeks and a rest interval of 2 minutes between exercises. The exercises will be taught to the patients at the end of the first session in both groups. The data will be analyzed using SPSS version 24 for Windows software. Statistical significance will be set at P ≤ 0.05. Normality of data will be assessed through Kolmogorov-smirnov test. Difference between pre-treatment and post-treatment readings will be calculated using Paired sample t-test for parametric data. For non-parametric data Wilcoxon test will be used. Independent sample t test will be used for parametric data and Mann Whitney test will be used for non parametric data.

Registry
clinicaltrials.gov
Start Date
March 9, 2024
End Date
July 30, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Muhammad Naveed Babur

Principal Investigator

Superior University

Eligibility Criteria

Inclusion Criteria

  • Age 30-50 years
  • Patient with the history of 3 months nonspecific low back pain
  • Pain intensity (3-7) according to VAS score

Exclusion Criteria

  • Spinal stenosis
  • Neurological dysfunction
  • Systemic disease
  • Pregnancy
  • Infections
  • Carcinoma
  • Any fracture or deformity

Outcomes

Primary Outcomes

VA

Time Frame: 6 Months

Visual Analogue Scale (VAS) is one of the pain rating scales 10 for worse and 0 for no pain

Secondary Outcomes

  • SF36(6 Months)

Study Sites (1)

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