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Clinical Trials/NCT05779891
NCT05779891
Recruiting
Not Applicable

Comparative Effects of Mulligan Straight Leg Raise Technique Versus Slump Stretching on Pain, Disability and Hip Range of Motion in Patients With Chronic Low Back Pain.

Sahreen Anwar1 site in 1 country48 target enrollmentMarch 7, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Low-back Pain
Sponsor
Sahreen Anwar
Enrollment
48
Locations
1
Primary Endpoint
Low Back Pain
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

The goal of this clinical trial is to examine the effect of mulligan straight leg raise versus slump stretching on pain, disability and hip range of motion in patient with low back pain. . Convenient sampling technique will be used to enroll the patients. Patients will be inquire into basis of pre formulated eligibility criteria. Written Consent will be taken from each patient before starting interventional sessions. Sample size of this study will consist on the participants who will qualify for both inclusion an exclusion criteria. Both groups will receive ultrasonic therapy and hot pack therapy as baseline treatment. Group A will receive mulligan straight leg raise and group B will receive slump stretching. The assessment of patients will be done at baseline, 4th and 8th week. The outcomes from patients will be calculated by using Visual Analogue Scale (VAS), Goniometer and ODI. The comparison between pre-treatment and post-treatment data will be done after 8th week. Data will be analyzed through SPSS 25.

Registry
clinicaltrials.gov
Start Date
March 7, 2023
End Date
June 30, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Sahreen Anwar
Responsible Party
Sponsor Investigator
Principal Investigator

Sahreen Anwar

Dr

Riphah International University

Eligibility Criteria

Inclusion Criteria

  • Patients who have active positive knee extension test(APKET).
  • Patient having low back pain for more than 3 months.
  • Patients who have been sitting for three hours.

Exclusion Criteria

  • Any active infection, tumor, tuberculosis.
  • History of trauma.
  • Subject with intervertebral disc prolapse.

Outcomes

Primary Outcomes

Low Back Pain

Time Frame: 8 weeks

Pain will be assessed by using Numerical Pain Rating Scale

Disability related to back pain

Time Frame: 8 weeks

Disability will be assessed by using Owestry Disability Index

Range of motion at hip joint

Time Frame: 8 weeks

Range of motion will be assessed by using Goniometer

Study Sites (1)

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