Skip to content

Effects of sacroiliac mobilization versus thrust manipulation on pain and functional disability in female patients with sacroiliac joint dysfunction

Effects of sacroiliac mobilization versus high velocity low amplitude thrust manipulation on pain and functional disability in female patients with sacroiliac joint dysfunction: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211117053085N1
Enrollment
72
Registered
2021-12-20
Start date
2021-08-04
Completion date
Unknown
Last updated
2022-01-11

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

Conditions

Sacroiliac joint Dysfunction. Sacroiliitis, not elsewhere classified

Interventions

Intervention 1: Intervention group: 1 will receive Mobilization along with Routine physical therapy. In routine physical therapy we will use electro therapeutic modalities and simple pelvic stabilizat

Sponsors

university of Lahore
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patients with confirmed clinical diagnosis of sacroiliac joint dysfunction will be included Patients presenting with acute pain from last four weeks in low back or Sacroiliac joint of iliac origin Patients with the complain of hypomobility of sacroiliac joint Will be included in our study Females from age 25 to 50 years will be included in our study

Exclusion criteria

Exclusion criteria: Patients with vertebral bone pathology,radiculopathy,sciatica, recent fracture will not be included in our study Patients with history of recent surgery in lumbosacral or pelvic area Females with history of osteoporosis or cancer or any other bone pathology will not be included Pregnant women, or those who had recent infection will not be included in our study

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: outcome will be measured at baseline, 1st, 2nd and 4th weeks post intervention. Method of measurement: pain will be measured using Numeric pain rating scale.;Functional Disability. Timepoint: Outcome will be measured at baseline, 1st, 2nd and 4th weeks post interventions. Method of measurement: Functional disability will be measured using Oswestry Disability Index Questionnaire.

Countries

Pakistan

Contacts

Public ContactDr. Wajida Parveen

Sialkot college of physical therapy

wajopri@gmail.com092333507157

Outcome results

None listed

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