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Clinical Trials/NCT05779891
NCT05779891RecruitingNot 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 Anwar2 sites in 1 country48 target enrollmentStarted: March 7, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
48
Locations
2
Primary Endpoint
Low Back Pain

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 25 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Sahreen Anwar
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Sahreen Anwar

Dr

Riphah International University

Study Sites (2)

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