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: Comparison of effects of lumbar stabilization exercises with and without respiratory resistance training among women with sedentary office workers affected by non-specific chronic low back pain

: Comparison of effects of lumbar stabilization exercises with and without respiratory resistance training on pain, disability and function among women with sedentary office workers affected by non-specific chronic low back pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241231064224N1
Enrollment
32
Registered
2025-01-12
Start date
2024-11-06
Completion date
Unknown
Last updated
2025-02-03

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. Non-specific chronic low back pain

Interventions

Intervention 1: Intervention group: lumbar stabilization exercises with respiratory resistance training , Exercises are performed 3 times a week for a duration of 4 weeks". Intervention 2: Control gr

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 49 Years

Inclusion criteria

Inclusion criteria: Being male or female. Age range between 25 to 49 years. Individuals who have been working in a sedentary environment for at least one year Individuals whose workplace requires them to sit for 8 to 11 hours daily Individuals who have not participated in any sports activities History of lower back pain for more than three months Presence of radiculopathy (nerve pain) is not acceptable. A pain score on the analog scale between 30 and 70 No history of back surgery. A score of more than 3 in the back functionality test is not acceptable No history of spinal column inflammatory diseases No history of scoliosis (curvature of the spine) No history of fractures in the spinal column No history of musculoskeletal and neurological diseases No history of systemic diseases or respiratory problems

Exclusion criteria

Exclusion criteria: Individuals who are pregnant Individuals with a body mass index (BMI) of 30 kg/m² or lower Individuals unable to perform tests or interventions due to pain. Individuals who have attended less than 80% of the treatment sessions. Individuals unwilling to continue treatment.

Design outcomes

Primary

MeasureTime frame
Pain visual analogue scale score. Timepoint: At the beginning of the study (before the intervention starts).At the end of the study (after the intervention sessions are completed). Method of measurement: 100 millimeters visual analog pain scale ruler.

Secondary

MeasureTime frame
Korean-Oswestry Disability Index(K-ODI). Timepoint: At the beginning of the study (before the intervention starts).At the end of the study (after the intervention sessions are completed). Method of measurement: Scores from Korean-Oswestry Disability Index(K-ODI).;The five repetitions sit to stand test (FRSST). Timepoint: At the beginning of the study (before the intervention starts).At the end of the study (after the intervention sessions are completed). Method of measurement: Timer.;The time of DUBOUSSET Functional Test. Timepoint: At the beginning of the study (before the intervention starts).At the end of the study (after the intervention sessions are completed). Method of measurement: Timer.;Average percentage of rib cage motion in manual assessment of respiratory motion in normal and deep breathing. Average balance of respiratory motion in manual assessment of respiratory movement in normal and deep breathing. Average volume of respiratory movement in manual assessment of respiratory motion in normal and deep breathing. Timepoint: At the beginning of the study (before the intervention starts).At the end of the study (after the intervention sessions are completed). Method of measurement: Using a square meter and placing it in the formula.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Sayadzadeh

Tehran University of Medical Sciences

fatemeh.s.zadeh@gmail.com+98 21 7753 3939

Outcome results

None listed

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