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The effect of mulligan and Maitland techniques in athletes with low back pain

Comparison of the effect of mulligan SNAG and Maitland mobilization techniques on the kinematic parameters of Lumbo-pelvic during stand to sit and sit to stand in athletes with Non- specific chronic low back pain

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160808029264N11
Enrollment
30
Registered
2021-06-18
Start date
2021-08-20
Completion date
Unknown
Last updated
2021-06-21

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

Conditions

Chronic low back pain. Low back pain

Interventions

Intervention 1: Intervention group 1: Participants in the first group will receive the Maitland Mobilization as an anterior-posterior glide, which is 4 days a week for 4 weeks and 16 sessions, each la

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: The age range of 18-50 years Having a VAS between 30-60

Exclusion criteria

Exclusion criteria: Diffuse pain with sciatic nerve root involvement History of surgery and fracture of the lumbar spine or other spinal structures BMI greater than 30 kg / m2 leg pain spreading below the knee paresthesia in the legs movement impairment or motor involvement in limb muscles Acute intervertebral disc herniation Malignancy Having any medical condition that has been contraindicated for exercise therapy Pregnancy Absence of radicular symptoms during daily activities especially walking Rheumatic and heart diseases Local swelling in the spine Skin changes in the spine due to skin problems and burns

Design outcomes

Primary

MeasureTime frame
Lumbo-pelvic kinematic. Timepoint: before and after treatment. Method of measurement: motion analysis system of qualysis.;Disability. Timepoint: Before and after treatment. Method of measurement: ODI Disability questionnaire.;Pain. Timepoint: Before and after treatment. Method of measurement: 100 mm VAS pain scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSahar Pishgoo

Semnan University of Medical Sciences

rasool.bagheri@ymail.com+98 23 3356 4180

Outcome results

None listed

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