Clinical trial · Observational
Female Cancer Patients' Preference For Sexual Health Interventions
A Pilot Study Surveying Female Cancer Patients' Preference For Sexual Health Interventions
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to survey female cancer patients' awareness of and preference for methods to improve sexual health. This information will help to improve our understanding of the needs and preferences for sexual health strategies and interventions of our female patients. The findings of this survey will also be used to develop feasible sexual health resources for our patients and enhance the success of grant proposals to support future sexual health interventions at MSKCC.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Gynecologic Cancer | Malignant Female Reproductive System Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (1)
- label
- survey
- description
- Participants will be asked to complete a survey as a one time assessment.
Primary outcomes (1)
- measure
- Participant' awareness of sexual health issues & preference for sexual health intervention
- timeFrame
- 2 years
Secondary outcomes (1)
- measure
- To assess & describe female cancer patients' attitudes towards & preference of methods to receive sexual health information (verbal or written) & psychosexual education patient information cards or intervention modality (telephone, in-person or online).
- timeFrame
- 2 years
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 21 Years
Show eligibility criteria text
Inclusion Criteria: * Participants must be able to communicate in English to complete the tests. * Study group of breast and/or gynecological cancer survivors. * History of Primary diagnosis of breast and/or gynecological cancer * At least 21 years of age. * In the judgement of the consenting professional able to provide informed consent * In the judgement of the consenting professional, able to communicate well enough in English through verbal and written communication to complete the study assessments. Exclusion Criteria: * In the judgement of the consenting professional, the individual is able to provide informed consent. * Patients with a psychiatric disorder precluding response to the surveys.
References
Publications (0)
Data not yet available