The effect of core stability and progressive postural control exercises in women with non-specific chronic low back pain

The effect of core stability and progressive postural control exercises on pain, disability and activity of hip and trunk muscles in women with non-specific chronic low back pain

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20250217064749N1

Enrollment

Registered

2025-03-01

Start date

2025-04-04

Completion date

Unknown

Last updated

2025-07-21

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. Dorsalgia, unspecified

Interventions

Intervention 1: Intervention group: core stability exercises: For eight weeks, they conduct three sessions per week, with each session comprising 30 minutes of core stability exercises. During the cou

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: non-specific chronic low back pain

Exclusion criteria

Exclusion criteria: Chronic back pain with traumatic or structural origin Back pain with neurological symptoms or radiating pain in the legs Without a history of previous back surgery tumors Spinal infections stroke Parkinson's Disease Multiple Sclerosis

Design outcomes

Primary

Measure	Time frame
Comparison of the reduction in pain scores on the Visual Analogue Scale (VAS) questionnaire. Timepoint: Pre- and post-intervention assessments following eight weeks of therapeutic exercise. Method of measurement: The Visual Analogue Scale (VAS) questionnaire.;Comparison of the Roland-Morris Disability Questionnaire (RMDQ) scores. Timepoint: Pre- and post-intervention assessments following eight weeks of therapeutic exercise. Method of measurement: The Roland-Morris Disability Questionnaire (RMDQ).;Evaluating muscle activity with an eight-channel surface electromyography system from Noraxon, USA. Timepoint: Pre- and post-intervention assessments following eight weeks of therapeutic exercise. Method of measurement: Eight-channel surface electromyography system from Noraxon, USA.	—

Measure

Time frame

Comparison of the reduction in pain scores on the Visual Analogue Scale (VAS) questionnaire. Timepoint: Pre- and post-intervention assessments following eight weeks of therapeutic exercise. Method of measurement: The Visual Analogue Scale (VAS) questionnaire.;Comparison of the Roland-Morris Disability Questionnaire (RMDQ) scores. Timepoint: Pre- and post-intervention assessments following eight weeks of therapeutic exercise. Method of measurement: The Roland-Morris Disability Questionnaire (RMDQ).;Evaluating muscle activity with an eight-channel surface electromyography system from Noraxon, USA. Timepoint: Pre- and post-intervention assessments following eight weeks of therapeutic exercise. Method of measurement: Eight-channel surface electromyography system from Noraxon, USA.

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Secondary

Measure	Time frame
Comparison of the reduction in pain scores on the Visual Analogue Scale (VAS) questionnaire. Timepoint: Pre- and post-intervention assessments following eight weeks of therapeutic exercise. Method of measurement: The Visual Analogue Scale (VAS) questionnaire.;Comparison of the Roland-Morris Disability Questionnaire (RMDQ) scores. Timepoint: Pre- and post-intervention assessments following eight weeks of therapeutic exercise. Method of measurement: The Roland-Morris Disability Questionnaire (RMDQ).;Evaluating muscle activity with an eight-channel surface electromyography system from Noraxon, USA. Timepoint: Pre- and post-intervention assessments following eight weeks of therapeutic exercise. Method of measurement: Eight-channel surface electromyography system from Noraxon, USA.	—

Measure

Time frame

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Haghshenas

Arak university

f.haghshenas.02@msc.araku.ac.ir+98 71 5382 4523

Outcome results

None listed

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