Comparison of Spinal Stabilization Exercises Vs Maitland Mobilization Along With Laser Therapy

June 14, 2022 updated by: Muhammad Naveed Babur, Superior University

Comparison of Spinal Stabilization Exercises Vs Maitland Mobilization Along With Laser Therapy in Non-Specific Low Back Ache

Comparison of Spinal Stabilization Exercises Vs Maitland Mobilization Along with Laser Therapy in Non-Specific Low Back Ache

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

Comparison of Spinal Stabilization Exercises Vs Maitland Mobilization Along with Laser Therapy for finding the better method for the treatment of Non-Specific Low Back Ache

Study Type

Interventional

Enrollment (Anticipated)

52

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Pakistan
      • Lahore, Pakistan
        • Al-Zahra Medical complex Johar town, Laser spine center Model town, Laser spine center Johar town.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Both male and female within the age range of 18-60 years.
  • Visual analogue scale that scores 3 and higher.
  • Non radiating low back pain

Exclusion Criteria:

  • Patients with a history of spinal diseases and injury
  • Spinal stenosis
  • Degenerative changes
  • Neuropathy
  • Intervertebral disc collapse.
  • Spinal discectomy
  • Spinal laminectomy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Spinal Stabilization Exercises
Spinal Stabilization Exercises technique
Behavioral: Spinal Stabilization Exercises
Spinal Stabilization Exercises technique
Experimental: Maitland Mobilization Along With Laser Therapy
Maitland Mobilization Along With Laser Therapy technique
Behavioral: Maitland Mobilization Along With Laser Therapy
Maitland Mobilization Along With Laser Therapy technique

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Spinal Stabilization Exercises in Non-Specific Low Back Ache
Time Frame: 6 Months
26 participants with the exercises include double knee to chest, single knee to chest, pelvic tilting,bridging and hamstring muscle stretching.(2) The stabilization exercises will be performed for 25 minutes. The patients will be educated on correct posture and starting positions for their exercises. Roland-Morris disability questionnaire to check the ovelall condition.
6 Months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maitland Mobilization Along with Laser Therapy in Non-Specific Low Back Ache
Time Frame: 6 Months
26 participants with the most commonly used Maitland technique is central posterior-anterior mobilization in which the therapist will perform 4 sets of mobilization for 30 seconds in grade I which will be administered to the three spinous processes around the most painful areas which will be followed by grade II with a rest interval of 30 seconds. Roland-Morris disability questionnaire to check the ovelall condition.
6 Months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Superior University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

June 1, 2022

Primary Completion (Anticipated)

August 1, 2022

Study Completion (Anticipated)

November 1, 2022

Study Registration Dates

First Submitted

May 5, 2022

First Submitted That Met QC Criteria

June 14, 2022

First Posted (Actual)

June 16, 2022

Study Record Updates

Last Update Posted (Actual)

June 16, 2022

Last Update Submitted That Met QC Criteria

June 14, 2022

Last Verified

June 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • DPT/Batch-Fall17/509

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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.

Subscribe