Pelvic Floor Muscle Biofeedback Device

Design, Development and Testing of Home-Based Non-Invasive Pelvic Floor Muscle Rehabilitation Device: A Multiphasic Exploratory Study - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/09/073809

Enrollment

Registered

2024-09-12

Start date

Unknown

Completion date

Unknown

Last updated

2024-09-16

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

Conditions

Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissue

Interventions

Intervention1: Pelvic Floor Muscle Biofeedback Device: This biofeedback device will help to strengthen and control their pelvic floor muscles activity. It will be given before and after 2 weeks of tre

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adults (25 years to 80 years of age group) 2. Patient with pelvic floor dysfunction (urinary 3. incontinence, pelvic organ prolapse, post-prostatectomy incontinence) Male and Female

Exclusion criteria

Exclusion criteria: 1. Recent pelvic surgery 2. Pregnancy 3. Severe cognitive impairment

Design outcomes

Primary

Measure	Time frame
PFDI (Pelvic floor dysfunction inventory) – 20 Timepoint: Baseline and after 2 weeks.	—

Secondary

Measure	Time frame
Quest 2.0Timepoint: After Completion of Intervention.	—

Countries

India

Contacts

Public ContactRuchi Sanjaykumar Bhuva

School of Physiotherapy, RK University

krupa.tank@rku.ac.in9998810063

Outcome results

None listed

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