ISRCTN86567908Completed未知
A randomised trial of a patient-centred strategy to facilitate transition of breast cancer survivors' routine Follow-UP from specialist to primary care
Canadian Breast Cancer Research Alliance/National Cancer Institute of Canada0 sites400 target enrollmentStarted: March 5, 2007Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Enrollment
- 400
Study Overview
Brief Summary
2014 results in: http://www.ncbi.nlm.nih.gov/pubmed/24326740
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Sex
- Female
Inclusion Criteria
- •1. Women diagnosed with invasive breast cancer
- •2. Stage I, II, or IIIa having completed primary treatment
- •3. There is no evidence of recurrence; and
- •4. Patient's surgeon agrees to transfer follow-up care to the Family Practitioner (FP)
Exclusion Criteria
- •1. Primary treatment (surgery, chemotherapy, radiotherapy) not completed at least three months previously, except for continued use of tamoxifen or an aromatase inhibitor
- •2. On herceptin or a potential candidate for herceptin (patients will become eligible following completion of herceptin therapy if ready for transition to primary care for routine follow-up)
- •3. Under investigation for possible recurrence (patients will become eligible if recurrence is ruled out)
- •4. Does not have a community-based FP to provide care (we will monitor the frequency with which patients are excluded because of this factor)
- •5. The patients' FP already has a patient enrolled in the trial (to avoid contamination)
- •6. Unable to comply with study protocol including completion of questionnaires
- •7. Previously enrolled in a study requiring ongoing follow-up by a cancer specialist; or
- •8. Actively followed by a cancer specialist for another primary cancer
Investigators
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