None listed
Conditions
Brief summary
This study is assessing the implementation of a model of shared care between cancer doctors and general practitioners to provide follow-up care to colorectal or prostate cancer patients Who is it for? You may be eligible to join this study if you are aged 18 years or above and receiving post active (follow-up) care for colorectal cancer or receiving ongoing surveillance of androgen deprivation therapy (ADT) for prostate cancer Study details Participants who opt into this study will receive a shared care plan provided to them by their treating specialists (Medical or Radiation Oncologist) that outlines follow up schedule, (shared care plan), including details of treatment and overall duration of follow up. Participants who opt out of the study will not receive a shared care plan but will continue with their routine follow up care. All participants will complete patient reported outcomes questionnaires at baseline, 6 and 12 months and the patient reported experience questionnaire at 12 months. The aim of this project is to integrate shared care models into CMN outpatient cancer services consistent with national guidelines and recommendations for care, improving access for new cancer patients and delivery of outpatient follow up care (including patient communication) to all patients.
Interventions
The aim of this project is to integrate shared care models into CMN outpatient cancer services, improving access for new cancer patients and delivery of outpatient follow up care (including patient communication) to all patients. the study will make an assessment of feasibility, application, acceptability and effectiveness of the shared model of care. The study is a feasibility evaluation using mixed-methods research. The components are: •Quantitative: Health service data of all patient participants engaged in the intervention groups and communication between cancer service and GPs. Patient reported outcome and experience measures will be collected throughout the feasibility evaluation (baseline, 6 months, 12 months). •Qualitative: Patient Participant interviews, GP, CMN cancer service staff survey and patient experience survey collected at the conclusion of the feasibility evaluation The project will commence with two patient cohorts with others added over time: 1. receiving post active (follow-up) care for colorectal cancer, Participants will attend their planned appointments per their shared care plan that will be provided to them by their treating specialists (Medical or Radiation Oncologist). in the first 12 months of follow up patients will attend 3 monthly follow up appointments that alternate between the treating team (Medical oncologist, surgeon) and their GP for patients with colon cancer and for patients with rectal cancer appointments with the treating team (medical and radiation oncologists and surgeon) and their GP, Appointments are generally face to face. or 2. receiving ongoing surveillance of androgen deprivation therapy (ADT) for prostate cancer Participants will attend their planned appointments per their personalised shared care plan that will be provided to them by their treating specialists (Medical or Radiation Oncologist). Participants will complete patient reported outcomes questionnaires at baseline, 6 and 12 months and the patient reported experience questionnaire at 12 months. Note there is no prescribed shared care schedule for prostate cancer patients receiving androgen deprivation therapy as the shared care plan is individualised by the treating clinician for each individual patient this includes follow up schedule with GP and any required PSA blood tests. All patients and GPs will be provided with a shared care schedule and follow up data collection via GP will be performed to ensure adherence to the schedule. Variation from the model included missed/delayed appointments, including 3 months or more from the scheduled appointment for scan or appointment with Specialist team or GP and /or 2 months for tumour markers will speak to the feasibility of shared care model.
Sponsors
Study design
Eligibility
Inclusion criteria
Target population: patients General Inclusion Criteria: • Patients over 18 years of age • Signed written informed consent. • Access to GP. • Capable of giving signed informed consent, which includes compliance with the requirements of the study. • Psychosocial needs have been assessed as not requiring ongoing specific psycho-oncology support. • GP consents to participate in shared care of the patient. Cohort specific inclusion - colorectal caner - All colorectal cancer patients who have received adjuvant chemotherapy (Stage II and III) - Patients receiving follow up care for colorectal cancer. - Adjuvant treatment completed within 12 months of consent. - Low risk of complications, with specifically the absence of evolving treatment related significant complications. - Patients are considered suitable if toxicities are categorized as either mild (Grade 1) or anticipated to be of prolonged duration or predicted to require several months for improvement and unlikely to necessitate substantial alterations in the typical follow-up strategy. Cohort specific inclusion- Prostate cancer - Patients receiving androgen deprivation therapy (ADT) or are receiving intermittent ADT for prostate cancer who commenced ADT treatment within 12 months of consent. - Patients who are receiving androgen deprivation therapy for prostate cancer and have been identified by treating team as stable.
Exclusion criteria
- Currently participating in another Clinical trial requiring ongoing follow up at CMN site. - Specific needs identified by treating clinician. - GP does not consent to participate in shared care of the patient Cohort specific exclusion criteria- colorectal cancer Exclusion Criteria - Metastatic resected or non-resectable disease. There is no cohort specific exclusion criteria for Prostate cancer cohort.