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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05280977
Enrollment
70
Registered
2022-03-15
Start date
2021-11-03
Completion date
2022-04-11
Last updated
2022-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Erector Spinae Tightness

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.

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.

Interventions

OTHERPOST 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.

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.

Sponsors

University of Lahore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
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.

Eligibility

Sex/Gender
ALL
Age
30 Years to 45 Years
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

Design outcomes

Primary

MeasureTime frameDescription
goniometer4 WEEKSRange 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

MeasureTime frameDescription
visual analog scale4 WEEKSThe 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

MeasureTime frameDescription
Oswestry Low Back Pain Disability Questionnaire4 WEEKSThe 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

Countries

Pakistan

Contacts

Primary ContactHaiderullah khan, MS PTN
haiderullah@live.com0092314127210

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026