- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07684118
Egoscue and Core Stabilization for Chronic Low Back Pain
Egoscue Based Postural Correction Combined With Core Stabilization Exercises in Patients With Chronic Low Back Pain
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Chronic low back pain (CLBP) is a highly prevalent musculoskeletal condition characterized by pain and discomfort in the lumbar region. It significantly affects functional activities, posture, mobility, and quality of life. Persistent low back pain may lead to muscle weakness, reduced spinal stability, limited range of motion, and increased disability in daily activities. Poor posture, especially lumbar hyperlordosis, is considered one of the contributing biomechanical factors associated with chronic low back pain. Core stabilization exercises are widely used in physiotherapy rehabilitation for chronic low back pain. Improvement in core muscle activation helps enhance spinal stability, reduce mechanical stress on the lumbar spine, improve functional performance, and decrease pain intensity.
Egoscue-based postural correction exercises are designed to improve body alignment, muscle balance, and postural symmetry through a sequence of therapeutic exercises. These exercises focus on correcting abnormal posture, restoring muscular balance, and improving movement patterns.
Although both core stabilization exercises and Egoscue-based postural correction exercises have individually shown beneficial effects in musculoskeletal rehabilitation, there is limited evidence regarding their combined effectiveness in patients with chronic low back pain associated with lumbar hyperlordosis.
Therefore, this randomized clinical trial aims to compare Egoscue-based postural correction combined with core stabilization exercises versus core stabilization exercises alone in patients with chronic low back pain.
Pain intensity will be measured using the numeric pain rating scale (NPRS), and functional disability Urdu Version of the Oswestry Disability Index (ODI). Secondary outcomes will include lumbar range of motion measured by inclinometer and posture/lumbar lordosis assessed by the Flexicurve ruler. The findings of this study may provide evidence regarding the effectiveness of combining Egoscue-based postural correction with core stabilization exercises for improving pain, disability, posture, and spinal mobility in patients with chronic low back pain.
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Punjab Province
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Lahore, Punjab Province, Pakistan, 54782
- The University of Lahore Teaching Hospital
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Patients aged 25-55 years , both genders
- Pain 4-7/10 (NPRS)
- Patients with chronic low back pain
- Hyperlumbar lordosis
Exclusion Criteria:
- Patients with lumbar radiculopathy
- Patients taking painkiller medications, patients with other spinal pathologies
- Patients with neurological conditions (e.g., stroke, multiple sclerosis), patients with any cardiac or psychological disorders
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Eksperimentel: Egoscue Exercises Combined with Core Stabilization Exercises
These patients will receive Egoscue-based postural correction exercises combined with core stabilization exercises alongside physiotherapy care for the management of chronic low back pain.
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Aktiv komparator: Core Stabilization Exercises
These patients will receive core stabilization exercises alongside physiotherapy care for the management of chronic low back pain with hyperlumbar lordosis.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Pain Intensity
Tidsramme: Baseline, 4th week and at 8 weeks of intervention
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Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS), an 11-point self-reported pain scale ranging from 0 to 10, where 0 = no pain and 10 = worst pain imaginable.
Higher scores indicate greater pain intensity (worse outcome)
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Baseline, 4th week and at 8 weeks of intervention
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Lumbar Range of Motion (ROM)
Tidsramme: Baseline, 4th week and at 8 weeks of intervention
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Lumbar spine range of motion measured using an Inclinometer, a reliable tool for assessing joint angle movement.
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Baseline, 4th week and at 8 weeks of intervention
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Postural Alignment
Tidsramme: Baseline, 4 weeks and at 8th week of intervention
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Lumbar lordosis and postural changes assessed using a Flexicurve Ruler, which measures spinal curvature by tracing the contour of the lumbar spine
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Baseline, 4 weeks and at 8th week of intervention
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Functional Disability
Tidsramme: Baseline, 4th week and at 8 weeks of intervention
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Functional disability will be assessed using the Urdu version of the Oswestry Disability Index (ODI).
The ODI consists of 10 items, each scored from 0 to 5, with a total score ranging from 0 to 50, which is commonly expressed as a percentage (0% to 100%).
Higher scores indicate greater disability and poorer functional status (worse outcome)
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Baseline, 4th week and at 8 weeks of intervention
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Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Studiestol: Sahreen Anwar, PhD, University of Lahore
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- UOL/IREB/25/12/0038
Plan for individuelle deltagerdata (IPD)
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