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Clinical Trial 22152

Cancer Type: Breast
Study Type: Other
NCT#: NCT05645471

Phase: N/A
Principal Investigator: Oswald, Laura

Call 813-745-6100
or 1-800-679-0775 Learn More
Overview

Study Title

Comparative effectiveness of Juntos Después del Cáncer (JDC) among Breast Cancer Survivors and their Intimate Partners

Summary

To evaluate the impact of an adapted online, self-help relationship intervention (supplemented with brief coach calls) for survivors of breast cancer and their partners. Couples will be randomized to receive either the online intervention (Together after Cancer) or usual care (UC) and assessed at baseline, end of the program, and 3 months after randomization.

Objective

To evaluate the impact of an adapted online, self-help relationship intervention (supplemented with brief coach calls) for survivors of breast cancer and their partners. Couples will be randomized to receive either the online intervention (Juntos Después del Cáncer; JDC) or usual care (UC) and assessed at baseline, end of the program, and 3 months after randomization. Examine whether survivors with poorer baseline psychological functioning experience greater benefit from the JDC intervention. Examine both quantitative and qualitative evaluations of the JDC intervention to maximize patient centeredness and opportunities for patient involvement in intervention development.

Treatments

Therapies

Medications

Inclusion Criteria

  • Inclusion Criteria for Latina Breast Cancer Survivors:
  • Be 18 years of age and older
  • Self-identify as Latina/Hispanic
  • Speak Spanish or English
  • Primary diagnosis of breast cancer in the last five years
  • Completed initial treatment
  • Be married or in a committed relationship of six months duration or longer
  • Willingness to be randomized and followed for approximately 5 months
  • Access to the internet or a smartphone, tablet, or computer
  • Inclusion criteria for Intimate Partners:
  • Be 18 years of age or older
  • Be married or in a committed relationship of six months duration or longer with a Latina Breast Cancer Survivor diagnosed who was diagnosed with breast cancer in the last five years
  • Willingness to be randomized and followed for approximately 5 months
  • Access to the internet or a smartphone, tablet, or computer
  • Couples will be eligible to participate if they also meet the following:
  • Meet the inclusion criteria listed above for Latina Breast Cancer Survivors and Intimate Partners
  • Both partners are willing to participate in the study
  • Additionally, to be eligible, the Latina Breast Cancer Survivors must reside in Florida

    • Exclusion Criteria

    If you are interested in learning more about clinical trials, our clinical trial navigators can discuss your options and recommend opportunities that may be suitable for you. Call 813-745-6100 or 1-800-679-0775 (toll-free) or submit a clinical trials inquiry form.

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