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Effectiveness Of Biofeedback And Pelvic Floor Exercises With Endometriosis Disease

Comparision of the effectiveness of biofeedback and pelvic floor exercises on the improving chronic pelvic pain and quality of sexual life in women with endometriosis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240619062179N1
Enrollment
96
Registered
2024-07-07
Start date
2024-09-05
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Endometriosis. Endometriosis, unspecified

Interventions

Intervention 1: Control group: (Group A) will receive only routine care(NSAID if needed) to relieve chronic pelvic pain. Intervention 2: InterventionIn group (B): addition to routine care, will recei

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Being married Having minimal reading and writing literacy Suffering from mild to moderate endometriosis Suffering from chronic pelvic pain for at least 3 months Reluctance to take hormone medication or contraindications to hormone therapy Aged between 18 and 45 years Surgery not indicated Suffering from spine diseases, discopathy, heart-disease and pulmonary failure, myopathy, cancer Increased intracranial pressure Not history of pelvic surgeries body mass index less than 30

Exclusion criteria

Exclusion criteria: The unwillingness of the participants to continue the interventions The occurrence of certain diseases or hip fractures after the start of the intervention (people who suffer during the interventions) Not complete more than 10% of the questionnaire Not participate in biofeedback sessions (at least 5 sessions) Not doing home exercises

Design outcomes

Primary

MeasureTime frame
Chronic pelvic pain. Timepoint: Before the start of the intervention and 8 weeks after the start of the intervention. Method of measurement: Visual Analogue Scale.;Quality of sexual life. Timepoint: Before the start of the intervention and 8 weeks after the start of the intervention. Method of measurement: Questionnaire of the sexual life quality of women, Simond et al., 2005.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Rastegari

Shiraz University of Medical Sciences

rastegari.zahra2015@gmail.com+98 71 3647 4254

Outcome results

None listed

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