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Impact of 6 week multimodal intervention program in managing hypotonic pelvic floor dysfunction among post menopausal women- a randomised control trial

Impact of 6 week multimodal intervention program in managing hypotonic pelvic floor dysfunction among post menopausal women- a randomised control trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099596
Enrollment
30
Registered
2025-12-22
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: N958- Other specified menopausal and perimenopausal disorders

Interventions

Intervention1: 6 WEEK MULTIMODAL INTERVENTION PROGRAM: six weeks protocol to patients with post-menopausal women with pelvic floor dysfunction. For the groups, five minutes of warm-up, thirty minutes

Sponsors

SGT University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.45-65 years old women 2.Clinical diagnosis or self-reported symptom of pelvic floor dysfunction.

Exclusion criteria

Exclusion criteria: 1.Urinary tract infection 2.Any neurological disorder 3.Recent Pelvic or abdominal surgery 4.Constipation 5.Pelvic malignancy

Design outcomes

Primary

MeasureTime frame
1.Perineometer 2.Pressure biofeedback 3.Pelvic pain impact questionnaire 4.International Consultation on Incontinence Questionnaire Urinary Incontinence (ICIQ-UI SF)Timepoint: baseline and after six week—

Secondary

MeasureTime frame
1.Bioelectrical impedance analysis 2.SF-12 questionnaireTimepoint: baseline & sixth week—

Countries

India

Contacts

Public ContactDr Priyanka Rishi

SGT University

Priyanka.sphy@sgtuniversity.org8588878467

Outcome results

None listed

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