Effects of a Sexual Health Enhancement Program for Women with Breast Cancer

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0010150

Enrollment

Registered

2025-01-24

Start date

2017-03-07

Completion date

Unknown

Last updated

2025-02-03

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

Conditions

None listed

Interventions

Others : The program consisted of four weekly 90-minutes face to face group intervention sessions, combined with two individual telephonic counseling sessions.

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Those who understand the purpose of the study and agree to participate Those who are between 20 and 60 years of age and have a spouse Those who have undergone mastectomy and have not had breast reconstruction Those diagnosed with breast cancer less than 5 years ago Patients who currently have no recurrence of breast cancer or metastasis to other organs Those who answered ‘yes’ to one or more questions assessing sexual problems in cancer patients according to the NCCN (2017) guidelines

Exclusion criteria

Exclusion criteria: Those who have been diagnosed with anxiety or depression by a doctor and are currently receiving medication

Design outcomes

Primary

Measure	Time frame
Sexual function	—

Secondary

Measure	Time frame
sexual distress;body image;marital intimacy;sexual knowledge	—

Countries

Korea, Republic of

Contacts

Public ContactHye Sook Kim

Seoul National University Hospital

khs369123@gmail.com+82-2-1588-5700

Outcome results