MFR Versus PFS Techniques on Pain,Range of Motion And Disability in Chronic Non Specific Low Back Pain.

Sponsor
Riphah International University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05811260
Collaborator
(none)
28
1
2
4
6.9

Study Details

Study Description

Brief Summary

To compare effect of myofascial Release versus post facilitation stretch in term of pain ,range of motion and disability in chronic non specific low back pain in patients.

Condition or Disease Intervention/Treatment Phase
  • Other: Myofascial Release technique
  • Other: Post facilitation stretch .
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
28 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effects of Myofascial Release Versus Post Facilitation Stretch Techniques on Pain,Range of Motion And Disability in Chronic Non Specific Low Back Pain.
Actual Study Start Date :
Mar 31, 2023
Anticipated Primary Completion Date :
Aug 1, 2023
Anticipated Study Completion Date :
Aug 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Myofascial Release

Group A (Myofascial release technique) on low back 3 repetitions (30 second rest between reps), lasting for 30 s for each myofascial track for 1 set to targeted muscles (plantar fascia, gastrocnemius, hamstrings, and erector spinae). The position will be held for 10-15 seconds when a pain point is found lacrosse ball excellent for this type of massage because their surface area is much less than that of foam rollers.

Other: Myofascial Release technique
on low back 3 repetitions (30 second rest between reps), lasting for 30 s for each myofascial track for 1 set to targeted muscles (plantar fascia, gastrocnemius, hamstrings, and erector spinae). The position will be held for 10-15 seconds when a pain point is found lacrosse ball excellent for this type of massage because their surface area is much less than that of foam rollers.
Other Names:
  • Myofascial Release technique for chronic non specific low back pain
  • Active Comparator: Post facilitation stretch

    Group B (Post facilitation stretch) static stretching exercises for the low back (plantar fascia, gastrocnemius, hamstrings, and erector spinae). Static stretching involved 3 sets of 3 repetitions for each muscle with a 30-second hold and 30-second rest interval for each repetition.

    Other: Post facilitation stretch .
    static stretching exercises for the low back (plantar fascia, gastrocnemius, hamstrings, and erector spinae). Static stretching involved 3 sets of 3 repetitions for each muscle with a 30-second hold and 30-second rest interval for each repetition.
    Other Names:
  • Post facilitation stretch for chronic non specific low back pain.
  • Outcome Measures

    Primary Outcome Measures

    1. . Numeric pain rating scale [4 weeks]

      NPRS is based on 11 points numerical rating scale for determining pain intensity, 0 ( no ;pain), 10 (worst pain imaginable).

    Secondary Outcome Measures

    1. Inclinometer [4 weeks]

      This instrument can measure Flexion, Extension, lateral flexion; a full range of tests ensures the best results. The Baseline Inclinometer is designed with your needs in mind; whether you need it for home or your professional clinic

    Other Outcome Measures

    1. Modified Oswestry Disability index [4 weeks]

      Urdu version of Modified Oswestry Disability Index has become one of the principal condition specific outcome measures used in the management of spinal disorders.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    40 Years to 55 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    Male and female adults already diagnosed with LBP Between ages group of 40-55 years.

    Exclusion Criteria:

    Patients who had LBP originating from various pathologies, such as presence of cord compression, radiculopathy, osteoporosis,

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 DHQ Layyah Punjab Pakistan

    Sponsors and Collaborators

    • Riphah International University

    Investigators

    • Principal Investigator: Muhammad Sanaullah, MS, Study principal Investigator

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Riphah International University
    ClinicalTrials.gov Identifier:
    NCT05811260
    Other Study ID Numbers:
    • REC/RCR&AHS/23/0106
    First Posted:
    Apr 13, 2023
    Last Update Posted:
    Apr 13, 2023
    Last Verified:
    Mar 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Riphah International University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 13, 2023