Comparison of the effect of two intervention methods (pelvic floor exercise and moisturizing cream) on sexual function and disparity in women undergoing systemic cancer

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190619043952N1

Enrollment

Registered

2019-08-20

Start date

2019-08-05

Completion date

Unknown

Last updated

2019-10-07

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

Conditions

breast cancer.

Interventions

Intervention group: Intervention group: First, Marin.F and Oxford Sexual Performance Inventory and a linear pain relief tool for one month. The moisturizing cream and the second one are performed for

Eligibility

Sex/Gender

Female

Age

25 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. The informed consent of the patient and his wife to enter the study2-Patients aged 20 to 50 years.3. Cancer that is systemically treated.4. Sexual dysfunction, which is specified in the FSFI questionnaire with a score below 25.5. Do not take medication to help improve sexual dysfunction and vaginal dryness if you take these medications before interrupting your medication.6. Non-incontinence of urine and stool and kidney and bladder cancer7. Not having a catration history in the last two months8. Not being treated for mental disorders (depression and anxiety).9-Urethrocole, Rectosyl and Cystocel grid 3 and above.10-Absence of vaginal infection and urinary tract infection11-Incidence of pelvic fracture12. Do not be breastfeeding

Exclusion criteria

Exclusion criteria: 1-Patient dissatisfaction with the continuation of the intervention2. Cancer recurrence and lack of response to treatment3-pregnancy

Design outcomes

Primary

Measure	Time frame
Sexual dysfunction. Timepoint: Sexual function measurement one month after the intervention, two months after the intervention and two months after the end of the intervention. Method of measurement: Sexual Function Questionnaire of Rosen Women, Marinop's Scale, Linear Pain Scale, Oxford Scale.	—

Secondary

Measure	Time frame
Pelvic floor exercise, moisturizing cream. Timepoint: Sexual function measurement one month after the intervention, two months after the intervention, and finally two months after the end of the intervention. Method of measurement: Rosen Sex Function Questionnaire, Linear Pain Tool, Marinop Scale, Oxford Scale.;Dyspuronia. Timepoint: Sexual function measurement one month after the intervention, two months after the intervention, and finally two months after the end of the intervention. Method of measurement: Rosen Sex Function Questionnaire, Linear Pain Tool, Marinop Scale, Oxford Scale.	—

Measure

Time frame

Pelvic floor exercise, moisturizing cream. Timepoint: Sexual function measurement one month after the intervention, two months after the intervention, and finally two months after the end of the intervention. Method of measurement: Rosen Sex Function Questionnaire, Linear Pain Tool, Marinop Scale, Oxford Scale.;Dyspuronia. Timepoint: Sexual function measurement one month after the intervention, two months after the intervention, and finally two months after the end of the intervention. Method of measurement: Rosen Sex Function Questionnaire, Linear Pain Tool, Marinop Scale, Oxford Scale.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactAhmad Nasiri

Birjand University of Medical Sciences

public_r@bums.ac.ir+98 56 3239 1406

Outcome results

None listed

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