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Recruiting NCT06694519

NCT06694519 Radiofrequency and Exercise-based Rehabilitation on Symptoms Associated With Pelvic Floor Dysfunctions in Breast Cancer

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Clinical Trial Summary
NCT ID NCT06694519
Status Recruiting
Phase
Sponsor SERGIO MONTERO NAVARRO
Condition Breast Cancer
Study Type INTERVENTIONAL
Enrollment 117 participants
Start Date 2025-01-30
Primary Completion 2025-12-30

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
manometry through the PHENIX series device (model: PHENIX LIBERTY; manufacturer: ELECTRONIC CONCEPT LIGNON INNOVATION, Montpelier, France).PFIQ-20 questionnaire (Pelvic Floor Impact Questionnaire Short Form)ICIQ-SF (International Consultation on Incontinence Questionnaire - Short Form)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 117 participants in total. It began in 2025-01-30 with a primary completion date of 2025-12-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Breast cancer has a high impact, affecting 2.3 million women worldwide in 2022. In Spain, there were 40,203 new cases in 2023. In addition to the economic and social costs, patients suffer genitourinary dysfunctions due to cancer treatments. Genitourinary Menopausal Syndrome (GUS) affects 50% of menopausal women, with a higher prevalence in women with breast cancer. This study aims to compare the effectiveness of radiofrequency (RF) and pelvic floor muscle exercise (PFMT) in the treatment of pelvic dysfunction associated with GUS in breast cancer patients. A randomised, double-blind clinical trial will be conducted in collaboration with the Association of Women Affected by Breast Cancer of Elche and Region) and the CEU Cardenal Herrera University. Women diagnosed with breast cancer and pelvic dysfunction will participate, divided into three groups: one will receive PFMT, one will receive RF and one will receive PFMT+RF therapy. Both techniques are expected to improve the quality of life of patients, where RF could offer additional benefits due to its proven effectiveness in the treatment of vaginal dryness and dyspareunia. The expected results will contribute to more effective and less invasive treatment protocols. The project presented has the potential to positively impact the health and well-being of women with breast cancer, reducing the symptoms associated with the disease and its treatment, and improving their quality of life.

Eligibility Criteria

Inclusion Criteria: * women of legal age with a clinical history of breast cancer, who agree to participate in the study and who present pelvic dysfunction assessed by the Pelvic Floor Distress Inventory (PFDI20) ≥ 100 * women survivors of stage 1 and 2 breast cancer * A medical discharge was granted more than one year ago * A diagnosis of another type of cancer has not been made. Exclusion Criteria: * Having performed PMFT or received RF in the last 12 months * Use of vaginal oestrogens in the last 6 months * Systemic hormone therapy in the last 6 months * Laser therapy in the last 6 months * Absence of pelvic floor contraction according to the Modified Oxford Scale * Use of pacemaker * Use of heart pacemaker, decompensated heart or metabolic diseases, cognitive deficits, peripheral or central neurological disorders, previous surgeries in the pelvic region, skin pathologies or wounds in the treatment area or presence of an active urinary tract and/or vaginal infection.

Contact & Investigator

Central Contact

SERGIO MONTERO-NAVARRO, PhD

✉ sergio.montero@uchceu.es

📞 +34 965426486

Principal Investigator

ANA LOZANO, MsC

PRINCIPAL INVESTIGATOR

CARDENAL HERRERA - CEU; CEU UNIVERSITIES

Frequently Asked Questions

Who can join the NCT06694519 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Breast Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06694519 currently recruiting?

Yes, NCT06694519 is actively recruiting participants. Contact the research team at sergio.montero@uchceu.es for enrollment information.

Where is the NCT06694519 trial being conducted?

This trial is being conducted at Elche, Spain.

Who is sponsoring the NCT06694519 clinical trial?

NCT06694519 is sponsored by SERGIO MONTERO NAVARRO. The principal investigator is ANA LOZANO, MsC at CARDENAL HERRERA - CEU; CEU UNIVERSITIES. The trial plans to enroll 117 participants.

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