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The effect of myofascial release of psoas major muscle on lumbar spine kinematic and disability in the subjects with non-specific chronic low back pain

The effect of myofascial release of psoas major muscle on lumbar spine kinematic and disability in the subjects with non-specific chronic low back pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150602022539N12
Enrollment
30
Registered
2022-04-19
Start date
2022-04-29
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Non specific chronic low back pain. Low back pain

Interventions

Intervention 1: Control group: Symbolically receives the technique of releasing the myofascia of the Psoas major muscle in four periods of two weeks and for forty minutes on both sides. Intervention 2

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Complete satisfaction to participate in this study People with nonspecific chronic low back pain with a minimum period of three months Age between 20-45 Pain intensity3-6 Bilateral shortening of psoas major muscle Disability grade 6-18 (from 24 points)

Exclusion criteria

Exclusion criteria: Pregnancy Having systemic fibromyalgia, Cauda equina syndrome, spinal tumor Having autoimmune, infectious, vascular, endocrine, metabolic and neoplastic diseases History of spinal surgery and other criteria contraindicating use of myofascial therapy Have previous experience in myofacial treatment or a history of low back pain rehabilitation treatment in the last two months

Design outcomes

Primary

MeasureTime frame
Angular velocity during stand to sit and sit to stand. Timepoint: Before and immediately after the two-week intervention and one month after the intervention. Method of measurement: Motion analysis device.;Angular displacement during stand to sit and sit to stand. Timepoint: Before and immediately after the two-week intervention and one month after the intervention. Method of measurement: Motion analysis device.;Maximum range of motion during stand to sit and sit to stand. Timepoint: Before and immediately after the two-week intervention and one month after the intervention. Method of measurement: Motion analysis device.;Disability. Timepoint: Before and immediately after the two-week intervention and one month after the intervention. Method of measurement: Ronald-Morris Questionnaire.;Relative phase during stand to sit and sit to stand. Timepoint: Before and immediately after the two-week intervention and one month after the intervention. Method of measurement: Motion analysis device.

Secondary

MeasureTime frame
Minimum phase angle during stand to sit and sit to stand. Timepoint: Before and immediately after the two-week intervention and one month after the intervention. Method of measurement: Motion analysis device.;Maximum phase angle during stand to sit and sit to stand. Timepoint: Before and immediately after the two-week intervention and one month after the intervention. Method of measurement: Motion analysis device.;Time to reach the maximum phase angle during stand to sit and sit to stand. Timepoint: Before and immediately after the two-week intervention and one month after the intervention. Method of measurement: Motion analysis device.;Time to reach the minimum phase angle during stand to sit and sit to stand. Timepoint: Before and immediately after the two-week intervention and one month after the intervention. Method of measurement: Motion analysis device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZiaeddin Safavi Farokhi

Semnan University of Medical Sciences

ziasafavi@yahoo.com+98 23 3365 4180

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026