Study on Sexual Health and Self-perceived Quality of Life (PROMs) in Patients Treated for Cervical Cancer

Starting soon · Phase 4

Conditions studied: Cervical Cancer

In brief

To assess the improvement in sexual function and self-perceived quality of life using PROMs (Patient-Reported Outcomes) in patients treated for cervical cancer who undergo a multimodal intervention in the sexual sphere and lifestyle compared to those who undergo care within routine clinical practice.

Key facts

Study ID

NCT07412873

Run by

Fundacion Clinic per a la Recerca Biomédica

People needed

120

Starts

2026-03-02

Expected to finish

2029-06-30

Last updated by the study team

2026-02-17

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women of legal age.
• Patients with primary cervical cancer stage FIGO I-III (initial or locally advanced) of squamous histology, adenocarcinoma or adenosquamous.
• Patients treated for cancer with surgery and/or radiotherapy ± systemic treatment in the Gynaecological Oncology Units of hospitals in Spain.
• Complete response after oncospecific treatment was obtained.
• Signature of the informed consent (IC) by the patient or responsible family member.

You may not qualify if…

• Patients under 18 years of age.
• Pregnancy or breastfeeding.
• Partial response after completion of oncospecific treatment.
• Patients with premalignant pathology.
• Diagnosis of a tumor of non-cervical origin or atypical histologies.
• Impossibility of completing the questionnaires included in the protocol autonomously.
• Contraindications to the use of vaginal estrogens.
• Patients undergoing fertility-sparing treatment (trachelectomy or conization).
• Patients undergoing palliative treatment.

Where it is running

• Laura Burunat — Teià, Barcelona, Spain

Full record on ClinicalTrials.gov

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