ACTRN12609000683235
Recruiting
未知
Evaluation of a Web-Based Cognitive Rehabilitation Programme in Cancer Survivors with Self Reported Cognitive Impairment
Dr Janette Vardy0 sites280 target enrollmentAugust 11, 2009
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Dr Janette Vardy
- Enrollment
- 280
- Status
- Recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Diagnosis of a primary malignancy for which definitive treatment was performed.
- •2\. Completed a minimum of 3 cycles of potentially curative chemotherapy within the last 6\-60 months.
- •3\. Aged 18 years and above.
- •4\. Self reported changes in memory and concentration as per the European Organisation for Research and Treatment of Cancer\-Quality of Life Questionnaire –C30 Cognitive Functioning scale (EORTC\-CF)
- •5\. Speak fluent English and read to a year 8 standard.
- •6\. Give written informed consent.
- •7\. Radiotherapy and/or immunotherapy (e.g. trastuzumab, lapatinib, bevacizumab or cetuximab) (if received) must have been completed at least 12 weeks prior to randomisation.
- •8\. Hormonal treatment (including tamoxifen or an aromatase inhibitor) is permitted providing treatment has been commenced at least 4 weeks prior to randomisation. Change of hormonal therapy should not be anticipated within the next 6 months, nor should it be likely to be ceased within 6 months.
- •9\. Easy access to computer and internet facilities.
- •10\. Participants are expected to be able to complete the study and be available for follow up.
Exclusion Criteria
- •1\. Eastern Cooperative Oncology Group (ECOG) Performance Status of \> 2\.
- •2\. Any evidence of locally recurrent or metastatic disease.
- •3\. Any active psychiatric diagnosis or history of a cognitive disorder. Psychotropic medications are permitted if the patient is established on a stable regime and dosing schedule.
- •4\. Pre\-existing neurological condition or any other co\-morbidity, which would interfere with their ability to perform cognitive testing.
- •5\. Prior malignancy within the last 5 years (other than non\-melanomatous skin cancer, cervical cancer in\-situ and the cancer of interest for which they received their chemotherapy).
- •6\. Any previous chemotherapy other than that given for the cancer of interest.
Outcomes
Primary Outcomes
Not specified
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