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EFFECTS OF YOGA, WILLIAM FLEXION EXERCISE, AND EDUCATION ON CHRONIC LOW BACK PAIN

EFFECTS OF YOGA, WILLIAM FLEXION EXERCISE, AND EDUCATION ON CHRONIC LOW BACK PAIN

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260711011
Enrollment
75
Registered
2026-07-11
Start date
2025-10-20
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

patients with chronic non-specific low back pain. Chronic Low Back Pain

Interventions

Participants received a structured therapeutic Yoga program focusing on spinal flexibility, core stabilization, breathing control, and relaxation techniques.,Participants received William Flexion Exer
Yoga Group,William Flexion Exercise Group,Education Group

Sponsors

No Sponsor
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Female rattan workers aged 30 to 65 years. 2. Chronic non-specific low back pain lasting more than 3 months. 3. No evidence of specific spinal pathology such as fracture, infection, tumor, or lumbar disc herniation. 4. Pain localized to the lumbar region without radiation to the lower extremities. 5. Not currently taking analgesic or pain-relieving medications. 6. Able to participate in exercise and educational sessions during the study period. 7. Willing to participate and provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Significant postural deformities including scoliosis, kyphosis, or hyperlordosis. 2. History of thoracolumbar fracture. History of spinal surgery. 4. Low back pain associated with radiculopathy or lumbar disc herniation, indicated by radiating pain and positive neurological tests. 5. Serious neurological, musculoskeletal, or systemic diseases that may interfere with participation. 6. Recent major trauma or fall involving the spine. 7. Inability to complete the intervention protocol or assessment procedures.

Design outcomes

Primary

MeasureTime frame
Pain Intensity 6 Weeks Visual Analogue Scale (VAS)

Secondary

MeasureTime frame
Trunk Muscle Activity 6 Weeks Surface Electromyography (sEMG),Functional Disability 6 Weeks Oswestry Disability Index (ODI),Sleep Quality 6 Weeks Pittsburgh Sleep Quality Index (PSQI)

Countries

Indonesia

Contacts

Public ContactErma Ginting

RS EFARINA ETAHAM SIANTAR

ermaginting00@gmail.com081264670767

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026