Marital Satisfaction and Sexual Health of Female Cancer Patients in Singapore
- Conditions
- Breast CancerGynecologic Cancer
- Interventions
- Behavioral: RISE
- Registration Number
- NCT03420547
- Lead Sponsor
- Duke-NUS Graduate Medical School
- Brief Summary
Disturbances in marital intimacy and sexual health is one of the most underrated and undertreated problems in cancer survivorship. A review on unmet supportive care needs of cancer patients noted one third to more than half of patients reported support for sexual disturbances as an area of unmet need during and after treatment. Patients, whose sense of femininity and body image may be at risk, such as in the case of breast and gynaecologic cancers, may be more susceptible to such intimacy and sexual disturbances. According to a recent study conducted in Singapore, 25% of gynaecologic cancer patients reported dissatisfaction with their bodies and 19% reported feeling less sexually attractive. Unfortunately, there is paucity in formal resources for couples counselling within the oncology setting in Singapore. The current study seeks to investigate a pilot program called Renewing Intimacy and Sexuality (RISE), which consists of 3 sessions with female cancer patients and their spouses, and that combine components of psychosexual education, communication training and skills building. The reach, acceptability, implementation, and preliminary effectiveness of the RISE program will be assessed based on the RE-AIM framework for program planning. The overall aim of the research project is to establish evidence-based programs for cancer survivors to enhance their quality of life.
- Detailed Description
This is a multi-site, randomized controlled, pilot intervention study. Patients seen in outpatient clinics in the Department of Gynaecologic Oncology at KKH Women and Children's Hospital (KKH) and the breast team within the Division of Medical Oncology at National Cancer Centre (NCC) will be recruited to participate. Patients who meet pre-screen criteria will be invited to complete a self-report screener of marital and sexual well-being. Those who are eligible for the study and indicate interest will be contacted to participate in the RISE program. Study participants will sign an informed consent before being given a pre-treatment assessment and being randomized using an opaque, sealed envelope system to receive either (i) the RISE program or (ii) Standard Care. Those in the Standard Care group will have the option of participating in the RISE program after their second pre-treatment assessment to ensure all participants are given the opportunity to receive the program. Randomization is stratified by cancer (i.e., gynaecologic vs breast) and occur in permuted blocks. At the end of participation in the RISE program, all participants will be given a post-treatment assessment. Spouse of the participants will be invited to participate in the study. Those who agree will complete a pre-treatment survey similar to the patient participant and attend the 3 sessions with the patient, and complete a post-treatment assessment similar to the patient's.
The RISE Intervention consists of 3 sessions which will last 2 hours each and be conducted with a clinical psychologist or medical social worker with experience with couples counseling. The intervention content include psycho-education, communication training between the couple, and exercises to foster intimacy. A therapy manual will be developed to ensure program delivery fidelity. A folder with session summaries will be provided to the participants.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 41
- Aged 21 years or old
- Has a spouse/ romantic partner
- History of stage I-III gynaecologic or breast cancer
- At least 4 weeks post completion of active treatment (i.e., surgery, chemotherapy, radiation therapy)
- Patient meets cut-off for marital distress on the Dyadic Adjustment Scale-4 (defined as overall score of ≤ 12) or sexual distress (defined as endorsing "occasionally" - "always" to the question how often patient felt distress about their sex life in the last 30 days)
- Speak and read English
-
Diagnosis of metastatic (stage IV) cancer
-
Visual, hearing, or cognitive impairment that will interfere with participation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention group RISE Group of participants receiving the RISE intervention
- Primary Outcome Measures
Name Time Method Collect feedback to improve the RISE program Week 6 for intervention arm; Week 12 for waitlist arm Obtained by conducting semi-structured interviews with participants at program completion.
Determine the acceptability of the RISE program Week 6 for intervention arm; Week 12 for waitlist arm Measured by participant rated satisfaction with the program using the Client Satisfaction Questionnaire
Assess the reach of the RISE program Baseline Measured by proportion of those who enrol to those who are eligible to participate.
Success of implementation of the program. Week 6 for intervention arm; Week 12 for waitlist arm Measured by participant's willingness to pay for the program.
- Secondary Outcome Measures
Name Time Method Preliminary data on effectiveness of the program. Change in scores from Baseline to Week 6 for intervention arm; change in scores from Baseline to Week 12 for Waitlist arm Measured by change in relationship well-being using the Dyadic Adjustment Scale-10
Trial Locations
- Locations (2)
National Cancer Centre
🇸🇬Singapore, Singapore
KK Women's and Children's Hospital
🇸🇬Singapore, Singapore