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The effect of manipulation on lumbar motion, pelvic symmetry and balance

Effect of manipulation on range and pattern of lumbar movement, pelvic asymmetry and postural sway in patients with pelvic dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201502187057N4
Enrollment
20
Registered
2015-03-22
Start date
2015-04-04
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Pelvic dysfunction. M25 (Sacro iliac joint dysfunctions)

Interventions

Intervention 1: Manipulation. Intervention 2: Not intervention.
Rehabilitation

Sponsors

Iran University of Medical Sience
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The patients with unilateral pelvic pain aged 18 to 50 years; anterior or posterior unilateral innominate rotation. Exclusion criteria: Creation of neural or spinal lesion or lumbar disc herniation; reumatoid disease?;previous surgery in lumbar region; osteoporosis? spondylolysthesis or lysis?;pregnancy and patients who were treated with manipulation 3 months ago.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Lumbar motion symmetry. Timepoint: The first time after subject’s entry into the study and the second time in two days later. Method of measurement: Using motion analysis system.;Sway area. Timepoint: The first time after subject’s entry into the study and the second time in two days later. Method of measurement: Using motion analysis system.;Pelvic symmetry. Timepoint: The first time after subject’s entry into the study and the second time in two days later. Method of measurement: Using a tape measure.

Secondary

MeasureTime frame
Oswestry Disability Questionnaire. Timepoint: The first time after subject’s entry into the study and the second time in two days later. Method of measurement: Using a questionnaire.;Pain intensity. Timepoint: The first time after subject’s entry into the study and the second time in two days later. Method of measurement: Using Visual analog scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Javad Mosavi

Deputy Director of Research and Technology, Iran University of Medical Sciences

research.m@iums.ac.ir+98 21 8670 2503

Outcome results

None listed

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