Clinical trial · Interventional
Trial to Evaluate an Educational Video Series for Women in Breast Cancer Treatment
Improving Breast Cancer Patients' Self-Efficacy and Sexual Health Quality of Life
- 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)
Approximately 200 English- or Spanish-speaking women newly diagnosed with stage I-III breast cancer will be randomized to either receive access to an online sexual health video series or receive usual care. Participants will complete surveys at baseline and every two months for six months, measuring self-efficacy in patient-provider communication and perceived barriers to discussing sexual health. Electronic health record review will assess utilization of sexual-health-related medical and supportive services. A subset of participants will participate in qualitative interviews to explore their sexual health experiences during treatment and, for those receiving the intervention, the perceived impact of the videos.
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 Females | — | UNRESOLVED | — |
| Newly Diagnosed Breast Cancer | Malignant Breast Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Sexual Health Educational Video Series | Behavioral | — | UNRESOLVED |
| Standard Care (in control arm) | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Intervention Arm
- description
- Participants receive access to the sexual-health educational video series.
- interventionNames
- Behavioral: Sexual Health Educational Video Series
- type
- PLACEBO_COMPARATOR
- label
- Control Arm
- description
- Participants receive standard care
- interventionNames
- Other: Standard Care (in control arm)
Primary outcomes (2)
- measure
- Participant self-efficacy discussing sexual health with breast cancer providers
- timeFrame
- Baseline, 2 months, 4 months, 6 months
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Provision to sign and date the consent form. * Stated willingness to comply with all study procedures and be available for the duration of the study. * Age minimum 18 * Be a female as assigned on birth certificate * Ability to read and speak English or Spanish * A recent diagnosis of Stage 1-III invasive breast cancer and receiving treatment for breast cancer at the University of Colorado or Denver Health breast center(s). Exclusion Criteria: * Age less than 18 years old * Stage 0 or Stage IV breast cancer * Prior breast cancer diagnosis * Non-breast cancer diagnoses * Prior exposure to anti-hormone therapy, chemotherapy, or radiotherapy not related to breast cancer
References
Publications (0)
Data not yet available