A Randomised Trial To Implement Systematic Distress Screening And Structured Care For Callers Using Cancer Councils' Telephone Services
Funder
National Health and Medical Research Council
Funding Amount
$289,279.00
Summary
Distress interferes with the ability to cope with cancer, its symptoms and treatment. Checking for distress and offering the right type of support should help reduce distress. In collaboration with state Cancer Councils, this study will test the costs and benefits of putting structured care into practice for people using Cancer Council telephone support services.
The Role Of Individual Patient, Social Support And Treatment Centre Variables In The Psychosocial Outcomes Of Cancer Patients
Funder
National Health and Medical Research Council
Funding Amount
$512,192.00
Summary
This national study, involving 20 medical oncology units, will be the first study of its kind to rigorously examine the role of individual patient (disease, demographic), social support, and treatment centre characteristics in psychosocial outcomes for cancer patients. Findings will give a bird’s eye view of which characteristics should be targeted to improve psychosocial outcomes for cancer patients.
Helping Family Caregivers Of Palliative Care Patients Manage Their Roles: Evaluation Of A Hospital Based Group Education
Funder
National Health and Medical Research Council
Funding Amount
$219,810.00
Summary
While most people would prefer to die at home, the reality is that about two thirds of people die in in-patient settings, such as palliative care units. A home death is more likely if family caregivers are well prepared and supported in their role. Palliative care services are expected to support family caregivers. Research shows, however, that many family caregivers lack the required information to effectively manage their role. They are also prone to suffer psychological distress while support ....While most people would prefer to die at home, the reality is that about two thirds of people die in in-patient settings, such as palliative care units. A home death is more likely if family caregivers are well prepared and supported in their role. Palliative care services are expected to support family caregivers. Research shows, however, that many family caregivers lack the required information to effectively manage their role. They are also prone to suffer psychological distress while supporting their dying relative. Caregivers have expressed a desire for structured information to better prepare them for their role, whether their dying relative is in hospital, a palliative care unit or at home. The aim of this project is to develop and evaluate an educational program offered to family caregivers who are supporting a relative who is receiving palliative care in an inpatient setting. The education program seeks to help family caregivers manage their role and to prepare them for the patient�s home care where appropriate. It is hoped that family caregivers who have attended the program will be more competent, better prepared and more informed about their caregiving role. An additional benefit from attending the program will be the opportunity for family caregivers to meet others in similar situations to themselves. Each education program will involve approximately six family caregivers; it will be conducted very soon after their relative has been admitted to the palliative care unit. The program will be of two hours duration (including time for data collection) and will be facilitated by a suitably qualified health professional. Written resources will be provided and caregivers will be given the opportunity to meet with staff from the multidisciplinary team. Referrals for scheduled consultations will be made where relevant. The program will be conducted in three sites (two in Victoria and one in Western Australia) and will be comprehensively evaluated. The caregivers who attend the program will be invited to provide feedback by completing several questionnaires designed to determine the effectiveness of the program. Group education programs of this kind have previously not been rigorously developed and tested. We seek to address this and hope to demonstrate that we can positively influence the family care giving experience.Read moreRead less
Patterns Of Care And Experience Of Care For Adolescents And Young Adults With Cancer
Funder
National Health and Medical Research Council
Funding Amount
$669,096.00
Summary
There is increasing concern, across several countries, that outcomes of care for adolescents and young adults (AYAs) with cancer are not optimal. This project aims to improve outcomes of care for AYAs with cancer by providing information about the best way to organise health services. It will do this by describing patterns of care for 700 AYA patients with cancer; providing detailed data on experiences with care for 300 patients; and conducting in-depth qualitative interviews.
A Randomised Controlled Trial Of The Cost-effectiveness Of Supportive Care Coordination For Advanced Cancer
Funder
National Health and Medical Research Council
Funding Amount
$147,269.00
Summary
The study will test the cost-effectiveness of two models of supportive care coordination for advanced cancer against usual care: a Telephone Caseworker model and an Oncologist-GP model. Both models are aimed at improving patients' and their informal caregivers' health and psychosocial status; are patient-centred, evidence based and readily transferable across health care settings. The Telephone Caseworker model has the additional advantage of reaching people isolated through geography, physical ....The study will test the cost-effectiveness of two models of supportive care coordination for advanced cancer against usual care: a Telephone Caseworker model and an Oncologist-GP model. Both models are aimed at improving patients' and their informal caregivers' health and psychosocial status; are patient-centred, evidence based and readily transferable across health care settings. The Telephone Caseworker model has the additional advantage of reaching people isolated through geography, physical disability or age.Read moreRead less
Predictors Of Psychological Distress In Adult Cancer Survivors:Development Of A Model For Tailoring Health Interventions
Funder
National Health and Medical Research Council
Funding Amount
$99,447.00
Summary
The number of people completing curative cancer treatment is increasing. Many cancer survivors report ongoing concerns with physical, psychological and social consequences of treatment. Little is known about how psychological distress differs between survivors. This research aims to develop an evidence-based model for tailoring interventions to different levels of distress and encouraging adoption of recommended health behaviours to improve survivor outcomes.
A Nurse Led Psychosocial Intervention With Peer Support To Reduce Needs In Women Being Treated With Radiotherapy For Gynaecological Cancer: A RCT
Funder
National Health and Medical Research Council
Funding Amount
$1,184,630.00
Summary
This study is to test the effectiveness of a nurse-led psychosocial intervention with peer support to reduce psychological distress, psychosocial needs, psychosexual difficulties and symptom distress and to improve quality of life and preparation for treatment of women receiving radiotherapy with curative intent for gynaecological cancer (GC) using a randomised controlled trial (RCT).