About this trial

The currently developed implementation study aims to evaluate if a patient-led home-based follow-up approach is successful, improves quality of life, reduces anxiety and lessens fear of cancer recurrence during the years after treatment of certain types of testicular cancer.

Eligibility criteria

Qualifiers

Age ≥ 18 years.

No lymphadenopathy or metastases on the postoperative scan.

Three consecutive blood drawings with normal tumour markers.

Patients undergoing lymph node dissection as a second curative operation after an orchiectomy, can also be included in case that the postoperative scan shows no residual disease or metastases.

Disqualifiers

Patients with aberrant levels of LDH preoperatively (LDH >248 U/L).

Patients enrolled in other studies that require strict adherence to any specific follow-up practice with regular imaging - yearly or more frequent - of the abdomen and/or thorax

Patients with comorbidity or other malignancy that requires imaging of the abdomen and/or thorax every year or more frequent

Inability to complete the questionnaires due to illiteracy and/or insufficient proficiency of the Dutch language

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

145 Participants
are grouped into 4 trial groups

Locations

1
Erasmus Medical Center3015GD, RotterdamSouth Holland, Netherlands

Sponsors and collaborators

Erasmus Medical Center

Lead sponsor