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Effects of Biofeedback on pelvic organ prolapse

A randomized controlled trial of biofeedback for quality of life in women with stages I and II pelvic organ prolapse

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015020620980N1
Enrollment
40
Registered
2015-04-17
Start date
2015-04-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

peivic organ prolapse. Diseases of the genitourinary system

Interventions

Intervention 1: Intervention: Biofeedback,Pelvic floor exercises, Life style modification. Intervention 2: Control: Pelvic floor exercises,Life style modification.
Rehabilitation
Intervention: Biofeedback,Pelvic floor exercises, Life style modification
Control: Pelvic floor exercises,Life style modification

Sponsors

Vice Chancellor for research of Iran University Of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion: women with stages I and II pelvic organ prolapse; women between ages 18-75 Exclusion: a history of pelvic surgery or delivery during recent 6 months; pelvic cancer;inability to pelvic muscles contraction;a history of surgery for prolapse;any kinde of low back pain which interfere the appropriate position for biofeedback;neurologic disorders;stages III and IV pelvic organ prolapse; a plan for pregnancy during next 2 months;any coincident therapies for prolapse;a plan of trip for more than 2 weeks during the intervention;Untreated UTI

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: basetime, 4 weeks and 12 weeks after intervention begins. Method of measurement: questionare.

Secondary

MeasureTime frame
Stage of prolapse. Timepoint: basetime,4 weeks and 12 weeks after intervention begins. Method of measurement: vaginal examination.;Pelvic muscles contraction force. Timepoint: basetime, 4 weeks and 12 weeks after intervention begins. Method of measurement: pressure biofeedback.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNeda Taghvadoust

Firoozgar Hospital

neda.taghvadoost@yahoo.com+98 21 8214 1612

Outcome results

None listed

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