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Effects of Manual Therapy Techniques for the Quadriceps Femoris on Pain and Lumbopelvic Alignment in Patients with Low Back Pain: A Randomized Controlled Trial

Effects of Manual Therapy Techniques for the Quadriceps Femoris on Pain and Lumbopelvic Alignment in Patients with Low Back Pain: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011970
Enrollment
40
Registered
2026-05-13
Start date
2026-04-06
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

None listed

Interventions

Others(manual therapy technique (soft tissue mobilization technique)) : Prior to the start of the study, the personal characteristics of the participants were investigated, and after administering the

Sponsors

Gachon University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Individuals aged 18 to 65 diagnosed with lumbar disc herniation 2) Individuals with concomitant quadriceps shortening (positive Ely’s test criteria) 3) Individuals with lower back pain scoring 3 or higher on the Numeric Rating Scale (NRS) within the last 3 months

Exclusion criteria

Exclusion criteria: 1) Individuals with a history of lumbar surgery 2) Individuals with lower back pain caused by structural lesions such as spinal stenosis or vertebral fractures 3) Individuals with radiating pain in the lower extremities or neurological deficits (muscle weakness, sensory abnormalities, etc.) 4) Individuals with musculoskeletal disorders of the hip joint or lower extremities 5) Individuals who have received injection treatment for lower back pain within the last 3 months

Design outcomes

Primary

MeasureTime frame
Low back pain

Secondary

MeasureTime frame
Lumabr Range of motion;Lumbar disability index;anterior pelvic tilt angle

Countries

Korea, Republic of

Contacts

Public ContactKangho Woo

Gachon University

dnrkdgh1@naver.com+82-32-820-4335

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Jul 23, 2026