None listed
Conditions
Brief summary
The purpose of this study is to test the feasibility of a care model involving haematologists and GPs for lymphoma follow-up care. Who is it for? You may be eligible for this study if you are aged 18 or older, and have lymphoma. Study details Participants in this study will be randomised by chance (like flipping a coin) into two groups. One group will receive standard follow-up (haematologist-led) care and information from Cancer Council Australia. The other group will undergo the share-care model. This involves a series of 20 to 60 minute appointments with specialist nurses, GPs and haematologists for up to 2 years. As part of the study all participants will answer a series of questionnaires every 6 months for 12 months. It is hoped this research will demonstrate the feasibility and usefulness of the new model of care which could influence future lympjhoma follow-up care.
Interventions
Group 1 (The shared-care group): Both acute post-treatment and observation follow-up patients will be offered 1 x 30-60 minute Nurse-led clinic within 10 weeks after the end of treatment and/or at least 2 weeks prior to the GP case-conference to: 1) provide survivorship patient education including a written survivorship booklet on “Living Well After Treatment – A guide for patients and families” published by Leukaemia Foundation; 2) treatment summary; 3) co-develop a Survivorship Care Plan (SCP) including SMART goals (using motivational interviewing and self-efficacy techniques); and 4) follow-up appointment schedule. A completed draft treatment summary and SCP will be provided to the GP. Both acute post-treatment and observation follow-up patients will be offered 1 x 20-30 minute case-conference between specialist nurse and GP after the Nurse-led clinic to discuss intervention follow-up schedule, the draft SCP with the GP and negotiate GP role in facilitating SCP goals and surveillance activities. A completed SCP will then be forwarded to the GP and the patient. After GP case conference, acute post-treatment follow-up patients will be offered 3 x GP appointments (at 3, 9 and 18 months) and 3 x Haematologist appointments (at 6, 12 and 24 months). All appointments will be of variable duration depending on patient need and clinician preference. After GP case conference, observation follow-up (i.e., surveillance clinics) patients will be offered 2 x GP appointments (at 6 and 18 months) and 2 x Haematologist appointments (at 12 and 24 months). All appointments will be of variable duration depending on patient need and clinician preference. All GP appointments will be to conduct surveillance activities (i.e., history and physical examination for B-symptoms and order and review of full blood count, urea and electrolytes, liver function tests and lactate dehydrogenase) and review the SCP, general health, and screening/management of comorbidities, psychosocial health cancer treatment toxicities, cancer-related symptoms; chronic disease management planning and allied health referrals. The GP will have direct telephone access to the specialist nurse in case of concerns or escalation for acute care review. All Haematologist appointments will be to conduct surveillance activities (i.e., history and physical examination for B-symptoms and order and review of full blood count, urea and electrolytes, liver function tests and lactate dehydrogenase). At 2 years, both acute post-treatment and observation follow-up patients will return to standard care practices (either discharge to GP or continued specialist surveillance).
Sponsors
Study design
Eligibility
Inclusion criteria
Due to the varying follow-up requirements for patients with lymphoma, we will recruit 2 groups of patients who map to 2 distinct follow-up pathways: - Group 1. Acute post-treatment follow-up: Patients with a pathologically confirmed diagnosis of aggressive or indolent lymphoma in the acute post-treatment phase (i.e., within three months of completion of chemotherapy); and - Group 2. Observation follow-up (i.e., surveillance clinics): Patients with a pathologically confirmed diagnosis of indolent lymphoma followed up in the surveillance clinic and at least 2 years post-treatment or treatment naïve. All participants must be: - Men or women - >/=18 years of age - have an ECOG performance status <2 - be an ambulatory patient at the time of recruitment - be able to nominate a GP to be involved in their follow-up - have access to a telephone
Exclusion criteria
- the presence of severe mental, cognitive or physical conditions that would limit the patient’s ability to participate as per treating clinician. - Lymphoma not in remission