NL-OMON55406
Completed
N/A
Cognitive functioning and health-related quality of life in long-term anaplastic oligondendroglioma and oligoastrocytoma survivors from the EORTC 26951 study: second follow-up - Follow-up of anaplastic oligondendroglioma and oligoastrocytoma patients
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- oligondendroglioma/oligoastrocytoma
- Sponsor
- Haaglanden Medisch Centrum
- Enrollment
- 12
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients are eligible for participation if they meet the following criteria:
- •1\) They are diagnosed with an anaplastic oligodendroglioma or oligoastrocytoma;
- •2\) They are adults; over 18 years old;
- •3\) They participated in EORTC 26951 study and the first follow\-up study;
- •4\) They have signed the informed consent form, or, when unable to decide, their
- •legal representative signed the informed consent form for their participation
- •and the use of their data., Proxies are eligible for participation if they meet
- •the following criteria:
- •1\) The patient is not deemed able to participate (as judged by the treating
- •physician) due to a poor physical or mental condition;
Exclusion Criteria
- •Patients are not considered eligible for study participation if:
- •1\) They are not eligible for participating in the study according to the
- •treating physician, due to severe physical or mental impairments hampering
- •filling in the questionnaires or undergoing the cognitive tests;
- •2\) They are unable to communicate adequately., Proxies are not considered
- •eligible for study participation if:
- •1\) They are unable to communicate adequately;
- •2\) The patient, or his/her legal representative, has not signed the informed
- •consent form for proxy participation;
- •3\) They proxy him\- or herself has not signed his/her own informed consent form.
Outcomes
Primary Outcomes
Not specified
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