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Clinical efficacy of diaphragmatic breathing training combined with biofeedback electrical stimulation therapy for postpartum stress urinary incontinence

Clinical efficacy of diaphragmatic breathing training combined with biofeedback electrical stimulation therapy for postpartum stress urinary incontinence

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073145
Enrollment
Unknown
Registered
2023-07-03
Start date
2023-07-10
Completion date
Unknown
Last updated
2023-07-10

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

Conditions

Postpartum stress urinary incontinence

Interventions

Vaginal delivery experimental group:biofeedback electric stimulation therapy combine with diaphragmatic breathing training
Vaginal delivery control group:biofeedback electric stimulation therapy
Caesarean section experimental group:biofeedback electric stimulation therapy combine with diaphragmatic breathing training
Caesarean section control group:biofeedback electric stimulation therapy

Sponsors

chengdu sport university
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
22 Years to 35 Years

Inclusion criteria

Inclusion criteria: ?Newborn mothers who have given birth for more than 3 months. ?Age 22 to 35 years. ?Lochia drains. ?Full-term delivery, singleton. ?Newborn baby weighing 2500-3500g. ?Prenatal Body Mass Index of between 18.5 and 23.9. ?Simple mild or moderate stress urinary incontinence or a diagnosis of pelvic. ?prolapse I-II using pelvic organ ?prolapse quantification (POP-Q) in women. ?No previous history of pelvic surgery or coexisting pelvic infections, no combined heart disease, diabetes, hypertension during pregnancy, no postpartum dysfunctional disorders prior to pregnancy.

Exclusion criteria

Exclusion criteria: ?Refusal to receive biofeedback electrical stimulation therapy for pelvic floor muscles. ?Refusal to undergo diaphragmatic breathing exercises. ?Edinburgh Postnatal Depression Scale (EPDS) summed to =13 points. ?Patients who do not agree to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Digital assessment of pelvic floor muscle strength;pelvic organ prolapse quantification;pelvic floor muscle bioelectrical activity;

Secondary

MeasureTime frame
pelvic floor distress inventory-short form 20;

Countries

China

Contacts

Public ContactMinjia Wang

Chengdu Sport University

wangminjia@cdsu.edu.cn+86 133 4096 1727

Outcome results

None listed

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