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new developed physiotherapy program in pregnant women with low back pain to reduce pain and improve activities of daily routine.

Effectiveness of newly developed structured physiotherapy protocol on pain,function and quality of life in sacroiliac joint dysfunction during pregnancy:A Randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/108609
Enrollment
90
Registered
2026-04-17
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium

Interventions

Intervention1: Newly developed structured physiotherapy protocol: The protocol will be finalized after validation by expert panel.All the exercises will be given in the range of 8-10 repetitions and

Sponsors

Dr Mithila Pawar
Lead Sponsor
DY Patil college of physiotherapy DY patil universityPune
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Pregnant women aged betwenn 18-35 years. 2. gestational age between second and third trimester 3. clinical diagnosis of sacroiliac joint dysfunction confirmed by more than or equal to 3 positive SI joint pain provocation tests. 4. complaint of pelvic girdle or sacroiliac joint pain. 5. ability to understand and follow instructions. 6. willingness to participate and provide written informed consent. 7. Primigravidas, Multigravidas 8. consent from gynaecologists

Exclusion criteria

Exclusion criteria: 1. High-risk pregnancy or obstetric complications 2. History of pelvic fracture, spinal surgery, or inflammatory arthropathy (3) 3. Neurological deficits or radicular symptoms 4. Severe symphysis pubis dysfunction 5. Any contraindication to physiotherapy intervention 6. Current participation in another interventional study

Design outcomes

Primary

MeasureTime frame
pain , functional disabilityTimepoint: baseline, 2 weeks post intervention, 6 weeks post intervention, every 2 weeks until delivery and 6 weeks post delivery

Secondary

MeasureTime frame
quality of lifeTimepoint: baseline, 2 weeks post intervention, 6 weeks post intervention, every 2 weeks until delivery and 6 weeks post delivery

Countries

India

Contacts

Public ContactDrMithila Pawar

Symbiosis college of physiotherapy,Symbiosis international deemed university

mithilapawarr3@gmail.com7798627730

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026