Effects of Mcgill versus Lee Stabilization Exercises on Pain, Disability, Range of motion, Quality of life and Endurance in Patient with Chronic Nonspecific Low Back Pain

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190717044238N14

Enrollment

Registered

2024-05-18

Start date

2024-05-20

Completion date

Unknown

Last updated

2024-05-27

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

Conditions

chronic non specific low back pain. M54.5

Interventions

Intervention 1: Intervention group: Mc Gill group. Intervention 2: Control group: Lee Stabilization.

Eligibility

Sex/Gender

All

Age

30 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patient with a history of 3 months nonspecific low back pain Pain intensity (3–7) according to NPRS score Age: 30–50 years Both male and female patients

Exclusion criteria

Exclusion criteria: Any lumbar surgery Spinal stenosis Neurological dysfunction Systemic disease Pregnancy Infections Carcinoma Any fracture or deformity

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: Before intervention, 6 weeks. Method of measurement: Numeric pain rating scale (NPRS).;Functional disability. Timepoint: Before intervention, 6 weeks. Method of measurement: Urdu version of Oswestry Disability index (ODI).;Range of motion. Timepoint: Before intervention, 6 weeks. Method of measurement: Inclinometer.;Endurance. Timepoint: Before intervention, 6 weeks. Method of measurement: Sorensen Test.;Quality of life. Timepoint: Before intervention, 6 weeks. Method of measurement: SF-36 Urdu version.	—

Measure

Time frame

Pain. Timepoint: Before intervention, 6 weeks. Method of measurement: Numeric pain rating scale (NPRS).;Functional disability. Timepoint: Before intervention, 6 weeks. Method of measurement: Urdu version of Oswestry Disability index (ODI).;Range of motion. Timepoint: Before intervention, 6 weeks. Method of measurement: Inclinometer.;Endurance. Timepoint: Before intervention, 6 weeks. Method of measurement: Sorensen Test.;Quality of life. Timepoint: Before intervention, 6 weeks. Method of measurement: SF-36 Urdu version.

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Countries

Pakistan

Contacts

Public ContactHafiza Sumbal Liaqat

Riphah International University Lahore

sumballiaqat10@gmail.com+92 332 0459833

Outcome results

None listed

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