Testicular Cancer Clinical Trial
— SCFU-TCOfficial title:
Shared Care Follow-up After Chemotherapy for Testicular Cancer
Verified date | May 2024 |
Source | University Medical Center Groningen |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The aim of this study is to develop and evaluate a shared care survivorship care plan (SCP) to follow-up patients with metastatic testicular cancer after completion of chemotherapy that resulted in complete remission.
Status | Active, not recruiting |
Enrollment | 163 |
Est. completion date | January 2025 |
Est. primary completion date | January 2025 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patients with disseminated testicular cancer; - Complete remission after chemotherapy with or without adjunctive surgery and in active follow-up; - Age 18 years or older; - Started with chemotherapy after January 1st 2003; - Written informed consent. Exclusion Criteria: •Mental disability |
Country | Name | City | State |
---|---|---|---|
Netherlands | University Medical Center Groningen | Groningen |
Lead Sponsor | Collaborator |
---|---|
University Medical Center Groningen |
Netherlands,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Safety of a shared care survivorship care plan (SCP). | The aim of this study is to develop and evaluate a shared care SCP to follow-up patients with disseminated TC after completion of chemotherapy. Participants in the SCP will be patients, GPs and oncologists. The SCP will be defined according to follow-up guidelines for TC patients, with a focus on disease relapse and late effects. | Monitoring of safety will be done on a continuous basis with average duration of two years per participant. | |
Primary | Feasibility of a shared care survivorship care plan (SCP). | The aim of this study is to develop and evaluate a shared care SCP to follow-up patients with disseminated TC after completion of chemotherapy. Participants in the SCP will be patients, GPs and oncologists. The SCP will be defined according to follow-up guidelines for TC patients, with a focus on disease relapse and late effects. | Monitoring of feasibility will be done on a continuous basis with average duration of two years per participant. | |
Secondary | Satisfaction with the SCP of testicular cancer survivors, GPs and oncologists. | The satisfaction with the SCP of testicular cancer survivors, GPs and oncologists will be evaluated by using questionnaires. | Up to two years. | |
Secondary | Willingness to migrate from hospital care to primary care. | The willingness to migrate from hospital care to primary care will be evaluated by specifying the decisions made within the SCP and by questionnaires to patients and GPs. | Up to two years. |
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