Effects of Posterior-anterior Vertebral Mobilization Followed by Prone Press-up Exercise in Nonspecific Low Back Pain

Last updated: November 10, 2024
Sponsor: Dr. Aftab Ahmed Mirza Baig
Overall Status: Completed

Phase

N/A

Condition

Chronic Pain

Treatment

Posterior-anterior vertebral mobilizations followed by Prone press-up exercise

Conventional physiotherapy

Clinical Study ID

NCT05997069
SindhIPMR
  • Ages 18-40
  • All Genders

Study Summary

Despite advances in intervention, many patients presenting with nonspecific low back pain (NSLBP) fail to have recovery from symptoms and activity limitation. Evidence suggests that interventions commonly used by physical therapists, may be effective for some but not all subsets of people with low back pain. Posterior anterior vertebral mobilizations (PAVMs) followed by prone press up (PPU) exercise are commonly used in clinical practice without a firm evidence. Research has shown this intervention decreases nonspecific low back pain on immediate effects but there is still limitation.The objective of this study is to determine the effects of posterior anterior vertebral mobilization followed by prone press-up exercise in comparison to conventional physiotherapy in nonspecific low back pain. The hypothesis is that the PAVMs followed by PPU exercise is more effective as compared to conventional physiotherapy to improve pain, lumbar range of motion, disability and quality of life in NSLBP. So, a randomized controlled trial will be conducted at Sindh Institute of Physical Medicine and Rehabilitation. One hindered and twenty patients with 18-40 years old having NSLB will be included on the basis of non-probability and purposive sampling technique and consent will be taken. Participants will be allocated into two groups through computer random sampling software. Experimental group will receive posterior-anterior vertebral mobilization followed by prone press up exercise and control group will receive conventional therapy (thermotherapy with general stretching exercises). All participants will be assessed using assessment form. After taking demo-graphical information, pain (in standing, sitting and walking), lumbar flexion and extension, functional disability and quality of life will be assessed before and after the treatment. All the data will be analysed for descriptive and inferential analysis.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Non-specific low back pain for more than 6 weeks.

  • Moderate intensity pain (3.5 -7.4 cm on Visual analogue scale)

Exclusion

Exclusion Criteria:

  • Subject whose current symptoms of low back pain provoke, or increase, and/orperipheralize (ie, pain reported to move from the midline laterally, or to thebuttocks, and/or lower extremity) with lumbar forward bending and prolonged sittingto a greater degree than with lumbar backward bending, or walking

  • Any history of trauma, fracture or surgical procedure of the lumbar spine.

  • Subjects administered epidural injections.

  • Low back pain due to specific pathology.

  • Any clinical condition that contraindicated physiotherapy intervention.

  • Subjects with neurological deficits (like stroke, Parkinsonism).

Study Design

Total Participants: 120
Treatment Group(s): 2
Primary Treatment: Posterior-anterior vertebral mobilizations followed by Prone press-up exercise
Phase:
Study Start date:
August 21, 2023
Estimated Completion Date:
November 08, 2024

Study Description

Initially, sample size of 38 was calculated through open epi software version 3.01 with 95% confidence interval and 80% power of test with post-test VAS mean (4.6) and standard deviation (1.2), in experimental group 17 and post-test VAS mean (3.6) and standard deviation (0.94) in control group on the basis of previous literature. Due to the low sample size at least 50 subjects per group were considered first. After including drop rate of 20%, 60 subjects per group will be considered with sample size of 120 participants having NSLBP. A maximum drop-out rate of 20% is assumed. All the data will be kept confidential. The privacy of all patients will be maintained. The patient recruitment, data collection, data management, data analysis, reporting for adverse events, and change management will be monitored by Institutional Review Board of the same institute. Data will be analysed using SPSS 23 version. Mean ± SD will be calculated of quantitative variables like age. Frequency and percentage will be calculated for qualitative variables. Intention to treat analysis will be used. The intra-group and inter-group analysis will be performed with two way repeated measure ANOVA. The p-value of 0.025 will be considered as level of significance.

Connect with a study center

  • Sindh Institute Physical Medicine and Rehabilitation

    Karachi, Sindh 74200
    Pakistan

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.