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Investigating the effect of sexual mindfulness-based training on sexual function and sexual well-being in women with breast cancer

Investigating the effect of sexual mindfulness-based training on sexual function and sexual well-being in women with breast cancer:A Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230416057924N1
Enrollment
30
Registered
2024-02-13
Start date
2024-01-10
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

Breast cancer. Malignant neoplasm of breast of unspecified site

Interventions

Intervention group: Intervention group: The members of the intervention group are trained in sexual mindfulness in 8 90-minute sessions by the researcher in collaboration with a clinical psychologist.

Sponsors

Shahre-kord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Having at least elementary education Iranian citizenship Definite diagnosis of breast cancer (pathological diagnosis) Informed consent to participate in the study Being sexually active Being single and living with a spouse now and during the study Not having sexual dysfunction before of cancer Absence of acute psychiatric disorders and use of related drugs Passing at least 3 months of conventional cancer treatments

Exclusion criteria

Exclusion criteria: Failure to participate in 2 or more sessions during the research period Using consulting services outside of research Divorce or death of spouse during the study period Existence of systemic or chronic disorders and any debilitating diseases such as heart disease, diabetes, etc Any use of sedatives, alcohol, psychotropic substances and drugs Diagnosing metastasis or disease recurrence Unwillingness to continue cooperation major depression

Design outcomes

Primary

MeasureTime frame
Sexual well-being. Timepoint: Start of the intervention - immediately and three months after the intervention. Method of measurement: Based on the scores obtained from the women's sexual well-being questionnaire:( Fsws scale).;Sexual function. Timepoint: Start of the intervention - immediately and three months after the intervention. Method of measurement: ( Female Sexual Function Index-FSFI).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAsefeh shirdashtzaeh

Shahre-kord University of Medical Sciences

st-shirdasht.a@skums.ac.ir+98 31 3272 3993

Outcome results

None listed

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