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Sexual Health in Breast Cancer Patients

University of Colorado Denver (CU Denver) logo

University of Colorado Denver (CU Denver)

Status

Completed

Conditions

Breast Cancer

Treatments

Behavioral: Focus Group

Study type

Observational

Funder types

Other

Identifiers

NCT05138510
NCI-2021-10894 (Other Identifier)
20-1789.cc

Details and patient eligibility

About

In the present study, we propose a mixed methods approach to characterize and address the sexual health needs among women with breast cancer at the time of diagnosis and throughout treatment.

Full description

In the present study, we propose a mixed methods approach to characterize and address the sexual health needs among women with breast cancer at the time of diagnosis and throughout treatment. The objectives are as follows:

  1. To characterize the sexual well-being of women longitudinally throughout the continuum of care, from initial diagnosis into survivorship.

    We predict that treatment will adversely affect sexual well-being, and that patient factors, clinical factors, and treatment choices will influence changes in sexual well-being.

  2. To identify gaps is sexual health education provided at the time of diagnosis or during treatment and to determine the appropriate timing of sexual health education delivery.

Enrollment

93 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients diagnosed with ductal carcinoma in situ or invasive breast cancer, seen in the breast center between 09/01/2019 to present, will potentially be recruited to participate.

Exclusion criteria

  • Patients less than 18 years of age and those with non-cancer diagnoses or prior history of breast cancer will be excluded.

Trial design

93 participants in 5 patient groups

Stage 0
Description:
Ductal carcinoma in situ. Timing: start of endocrine therapy
Treatment:
Behavioral: Focus Group
Stages I-III Surgery first
Description:
Invasive cancer. Surgery first Timing: start of endocrine therapy
Treatment:
Behavioral: Focus Group
Stages I-III, neoadjuvant chemotherapy first
Description:
Invasive cancer. Neoadjuvant chemotherapy first Timing: during neoadjuvant chemotherapy
Treatment:
Behavioral: Focus Group
Stage IV
Description:
Metastatic cancer, chemotherapy only, no invasive surgery Timing: 2 months into treatment
Treatment:
Behavioral: Focus Group
Survivors
Description:
Timing: any time
Treatment:
Behavioral: Focus Group

Trial contacts and locations

1

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Central trial contact

Victoria Huynh

Data sourced from clinicaltrials.gov

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