Effects Of Post Isometric Relaxation And Post Facilitation Stretching On ROM, Pain And Functional Limitations

Sponsor
University of Lahore (Other)
Overall Status
Recruiting
CT.gov ID
NCT05280977
Collaborator
(none)
70
1
2
5.2
13.4

Study Details

Study Description

Brief Summary

Study Design: Randomized Controlled Trial treatment techniques: post isometric relaxation and post facilitation stretching technique sample size: 35 in each group single blinded Before giving either treatment to each group, baseline data will be collected from each participant and then after 4th week of treatment.

Condition or Disease Intervention/Treatment Phase
  • Other: POST ISOMETRIC RELAXATION
  • Other: POST FACILITATION STRETCHING
N/A

Detailed Description

To compare the effects of post isometric relaxation and post facilitation stretching on Rom, pain and functional disability in patients with erector spinae tightness.Study Setting: Bahria International Hospital, Lahore Data will be analyzed using SPSS version 26.The quantitative variables like range of motion will be presented in the form of mean ±SD and qualitative variables like pain and functional disability will be presented in the form of frequency and percentage.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
The study will be single blinded as the assessor will be unaware of the treatment that will be given to both groups.
Primary Purpose:
Treatment
Official Title:
Comparative Effects Of Post Isometric Relaxation And Post Facilitation Stretching On Range Of Motion, Pain And Functional Limitations In Patients With Erector Spinae Tightness: A Randomized Controlled Trial
Actual Study Start Date :
Nov 3, 2021
Anticipated Primary Completion Date :
Apr 2, 2022
Anticipated Study Completion Date :
Apr 11, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: POST ISOMETRIC RELAXATION

Other: POST ISOMETRIC RELAXATION
Group A (Post Isometric Relaxation + Conventional Physiotherapy): This group will receive Muscle Energy Technique in addition to conventional physiotherapy for the treatment of erector spinae tightness. The treatment will be given on alternate days for four weeks with 8 - 10 repetitions of METs per session.

Experimental: POST FACILITATION STRETCHING

Other: POST FACILITATION STRETCHING
Group B (Post Facilitation Stretching + Conventional Physiotherapy): This group will receive Post Facilitation Stretching Technique in addition to conventional physiotherapy for the treatment of erector spinae tightness. The treatment will be given on alternate days for four weeks with 8 - 10 repetitions of METs per session.

Outcome Measures

Primary Outcome Measures

  1. goniometer [4 WEEKS]

    Range of motion will be measured by using universal standard goniometer.The goniometer comprises a body (rotation axis) with two arms attached to it, one being fixed and the other movable. The measurement of the ROM is performed by direct reading of the angle between the axis of rotation at the end of the active ROM of the movement assessed.

Secondary Outcome Measures

  1. visual analog scale [4 WEEKS]

    The Visual Analogue Scale (VAS) is an instrument for the measurement of subjective characteristics or attitudes that cannot be measured directly. It consists of a horizontal line with markings from 0 - 10 where "0" represents "no pain" and "10" represents "worst pain possible". The patient is asked to mark the number on the scale which best describes the level of his/her pain.

Other Outcome Measures

  1. Oswestry Low Back Pain Disability Questionnaire [4 WEEKS]

    The Oswestry Low Back Pain Disability Questionnaire is designed to assess the level of functional limitations or disability in activities of daily living of the patients with acute or chronic low back pain. It gives subjective percentage score. The questionnaire consists of 10 questions each having 6 options. Each option carries from 0-5 marks in descending order. The total score of the questionnaire is 50 while the minimum score is 0. The patient is asked to fill the questionnaire and their level of disability is assessed by scoring in the end. Their attained score is divided by the total score i-e 50 and is then divided by 100 to get the percentage

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • • Pain in lower back for atleast 4 weeks but less than 1 year.

  • Pain relieved by rest.

  • Decreased flexion, extension and lateral flexion of lumbar spine.

  • Individuals having no signs of nerve root irritation (dermatomal pain and paresthesia) and nerve root compression (dermatomal sensory loss, myotomal weakness, loss of reflex)

  • Age group: 30 - 45 years

  • Both male and female

Exclusion Criteria:
  • Individuals having other lumbar pathologies like disc problems, ligamentous strains, sciatica etc

  • Individuals having any inflammation and malignancy.

  • Pregnancy

  • Individuals having recent trauma, fracture, or surgery

Contacts and Locations

Locations

Site City State Country Postal Code
1 Bahria International Hospital Lahore Lahore Punjab Pakistan 54590

Sponsors and Collaborators

  • University of Lahore

Investigators

  • Principal Investigator: SYEDA RAHAT JABEEN, MSPT, THE UNIVERSITY OF LAHORE

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of Lahore
ClinicalTrials.gov Identifier:
NCT05280977
Other Study ID Numbers:
  • IRB-UOL-FAHS/1027/2021
First Posted:
Mar 15, 2022
Last Update Posted:
Mar 15, 2022
Last Verified:
Mar 1, 2022
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

Study Results

No Results Posted as of Mar 15, 2022