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How a specific treatment plan affects pain, muscle strength, functional disability and quality of life in lower back

Effect of selective treatment protocol on pain, muscle strength, functional disability and quality of life in sacroiliac joint dysfunction- A Randomized Controlled Trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/096894
Enrollment
82
Registered
2025-11-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: M248- Other specific joint derangements,not elsewhere classified

Interventions

Intervention1: Selective Treatment Protocol: WEEK 1 -Hot water fomentation (10 mins) -Ultrasound (5 mins) (Intensity of 1.3 W/cm2 and frequency of 1 MHZ in a continuous mode) -Hamstring stretch (Affec

Sponsors

Dr APJ ABDUL KALAM COLLEGE OF PHYSIOTHERAPY
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Unilateral sacroiliac joint dysfunction. 2)A pain score of equal to and more than 3/10 on visual analog scale (VAS) for sacroiliac pain in last 1.5 months. 3)Quadratus lumborum MMT 3 4)Pre diagnosed case 5)Using no other nonsteroidal anti-inflammatory drugs during the therapy. 6)Patients volunteered to participate in the study and signed informed consent

Exclusion criteria

Exclusion criteria: 1)Radiating pain. 2)Dislocation in lower back and lower extremity, fractures. 3)History of trauma. 4)Any systemic and metabolic disease. 5)Any rheumatologic disease. 6)Existence of known central nervous system or peripheral nervous system disease. 7)Pregnancy. 8)Involved in other treatments for pain relief.

Design outcomes

Primary

MeasureTime frame
1)Visual Analogue Scale (VAS) 2)Modified Oswestry Disability Questionnaire 3)Short form 12 questionnaire (SF-12) 4)Manual Muscle Testing (MMT) of Quadratus LumborumTimepoint: All outcomes measured at baseline and after 6 weeks.

Secondary

MeasureTime frame
1)Visual Analogue Scale (VAS) 2)Modified Oswestry Disability Questionnaire 3)Short form 12 questionnaire (SF-12) 4)Manual Muscle Testing (MMT) of Quadratus LumborumTimepoint: All outcomes measured at baseline and after 6 weeks.

Countries

India

Contacts

Public ContactANUSHKA A HASHIA
drneerajpt@gmail.com9005411557

Outcome results

None listed

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