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The effect of squatting on low back pain caused by prolonged standing

The influence of intermittent squatting on low back pain alleviation, activation of trunk and pelvis muscles and lumbopelvic kinematics in pain-developer subjects in prolonged standing

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090203001637N13
Enrollment
26
Registered
2022-01-17
Start date
2022-01-21
Completion date
Unknown
Last updated
2022-02-07

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

Conditions

Evaluation of the effectiveness of intermittent squatting in reducing low back pain caused by prolonged standing.

Interventions

Intervention 1: Intervention # 1: Participants stand for only 2 hours on the day of control and while working with a computer, the electromyographic and kinematic data will be recorded as "control dat

Sponsors

Tarbiat Modares University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 45 Years

Inclusion criteria

Inclusion criteria: Healthy men and women 25 to 45 years old interested in volunteering for a research project Having a BMI between 20 and 25 No history of low back pain in the last 12 months or musculoskeletal diseases related to the lower back and upper and lower limbs

Exclusion criteria

Exclusion criteria: Having the experience of low back pain in the last 12 months that requires a visit to a doctor, physiotherapist, chiropractor, or leave of absence more than three days from work or university Having professional and regular sports activities Having deformity or no arch of the foot (flat foot) Having any deformity in the spine and other limbs Having Uncontrolled blood pressure Factors affecting the ability of individuals to complete the test, such as cardiovascular or respiratory disorders Presence of low back pain or any musculoskeletal pain in the limbs on the test day Any back or thigh surgery Taking any analgesics or Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) 48 hours before the test Having a history of musculoskeletal pain in the hip, knee and ankle in the past year Inability to standing for more than 4 hours Inability to complete the questionnaires Employment in a job that requires long static standing in the last 12 months Reluctance to continue participating in the research project

Design outcomes

Primary

MeasureTime frame
Lumbar Lordosis. Timepoint: Every 15 minutes. Method of measurement: Vicon system.;Lumbar-pelvic-thigh angle. Timepoint: Every 15 minutes. Method of measurement: Vicon system.;Lumbar flexion angle. Timepoint: Every 15 minutes. Method of measurement: Vicon system.;Trunk Muscles Activation. Timepoint: Every 15 minutes. Method of measurement: Electromypgraphy system.;Trunk muscles co-contraction Ratio. Timepoint: Every 15 minutes. Method of measurement: Mathematics equation.

Secondary

MeasureTime frame
Severity of pain. Timepoint: Pre and post intervention. Method of measurement: Visual Analog Scale (VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarjan Ghavipisheh

Tarbiat Modares University

marjan.ghavipisheh@modares.ac.ir+98 21 8609 3437

Outcome results

None listed

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