University of Sydney
MPRU
 
 
MPRU History

The Medical Psychology Unit was formed in 1984 by Dr Stewart Dunn (psychologist) and Prof John Turtle, Professor of Medicine and Head of the Department of Endocrinology at the University of Sydney, to conduct research combining the principles of Psychology and Medicine in diabetes. In 1988, Dr Dunn began working with Prof Martin Tattersall (medical oncologist) and expanded the work of the Unit into cancer. The Unit was based in the Faculty of Medicine, Central Clinical School at the University of Sydney, and was co-directed by Dr Dunn and Prof Tattersall. Early research included developing measures of psychological adjustment to diabetes and cancer, exploring psychological predictors of outcome in melanoma and breast cancer patients, and developing an interaction analysis system to code audio-taped oncology consultations. 

Beginning with a staff of three, the Unit rapidly expanded, and by 1994 had a staff of 12, funded entirely by peer reviewed grants. Dr Phyllis Butow joined the staff in 1989 and became Deputy Director in 1992. In 1996, Professor Dunn moved to the Northern Clinical School and founded the Pam McLean Cancer Communications Centre. Dr Butow became co-Director of the Unit, based half time at the Northern and half-time at the Central Clinical Schools. The Unit changed its name to the Medical Psychology Research Unit (MPRU) in 1997 to better capture its focus. 

In 2002, Prof Butow was awarded an NHMRC Research Fellowship and returned full-time to the Central Clinical School. With increasing responsibilities in teaching and administration, Prof Dunn resigned as Co-Director but has maintained an affiliation with the Unit, particularly in the application of communication research to communication skills training for health professionals.

In 2003, Prof Butow accepted an appointment to a Chair in Psychology at the University of Sydney and the MPRU became a cross-Faculty Unit in the Faculty of Medicine and the School of Psychology. Dr Melanie Price joined the MPRU in 2004 and became Deputy Director in 2006.

Currently the MPRU has (including the Directors) 28 staff including 10 post-doctoral senior researchers. The MPRU has built an international reputation in the area of Psycho-Oncology and doctor-patient communication. It has been extremely successful, demonstrating its capacity to bring in funds and personnel to the University. Professors Butow and Tattersall are currently Chief Investigators on projects which have received competitive funding for over $8,000,000. Since 1995, the group has won 63 peer reviewed grants, attracted over $16,000,000 in research funds and published over 170 articles in high impact factor journals.

Recently, the MPRU has joined forces with the Sydney Health Decision Making Group in the School of Public Health to form a Centre for Medical Psychology and Evidence-based Decision Making within the University.


Research Interests

The MPRU has research interests in a wide arena, falling under the discipline of Health Psychology. These include: psychosocial predictors of the development and outcome of disease, the psychological impact of disease, factors influencing coping and adjustment to disease, development and evaluation of interventions to enhance health professional-patient communication, psychometric measurement and test development. These are described in more detail below.

1. Doctor-patient communication

2. Cultural aspects of cancer care

3. Psychosocial predictors of the development and outcome of disease

4. Psychological adjustment to illness and improving quality of life

5. Genetic counseling and testing

6. End of life issues

1. Doctor-patient communication
See Current Research Projects

Patients with cancer grapple with many difficult issues. They need to cope with bad news, take in complex and new information, make difficult decisions about treatment, and deal with the impact of disease on themselves, their partners and their family. Doctors and other health professionals can assist patients throughout this journey; research is needed to facilitate this process. Recognition of the importance of this area is reflected in the increasing attendance at communication skills training courses. Specific areas we have been researching include:
  1. Interaction analysis (coding) of doctor-patient communication
  2. Development and evaluation of strategies to improve doctor-patient communication and promote shared decision-making, including the provision of question prompt lists, letters summarising the consultation, audiotapes of the consultation and decision aids
  3. Auditing and improving the process of informed consent to standard treatments and clinical trials
  4. Evaluation of the impact of communication skills training on doctor and patient outcomes
  5. Development of guidelines in communicating risk and prognosis These strategies are now being applied in other areas, for example, provision of tapes to parents of babies in neonatal intensive care units; information needs re screening in healthy populations.

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2. Cultural aspects of cancer care
See Current Research Projects

Australia is a multi-cultural society, and principles of care developed in Western societies do not always transfer to other cultures. Specific areas we have been researching include:
  1. Preferences for communication of the diagnosis and prognosis in the Greek and Chinese communities

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3. Psychosocial predictors of the development and outcome of disease
See Current Research Projects

There has been a long-term interest in the role of psychosocial factors in promoting disease, or affecting its outcome. Most of the work in this area has been flawed by methodological shortcomings. Specific areas we have been researching include:
  1. Exploring the role of stress, personality, social support and coping style in the outcome of primary and secondary cancer
  2. Development and evaluation of an intervention to increase optimism and minimisation of the impact of cancer to promote longer survival
  3. Exploration of the role of stress, coping and social support in promoting breast cancer development in women from high risk breast cancer families.

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4. Psychological adjustment to illness and improving quality of life
See Current Research Projects

Research has been conducted on the psychosocial outcomes of cancer across time, including rates of anxiety and depression, sexual and relationship outcomes and quality of life. Interventions to improve adjustment are needed. Specific areas we have been researching include:
  1. Documenting unmet needs and quality of life outcomes over time in different diseases and different stages, including the survival phase
  2. Impact of informal and formal support networks on quality of life
  3. Documenting psychosexual outcomes following treatment for gynaecological cancer and developing interventions to improve these
  4. Evaluation of the effectiveness of different types of cancer support groups
  5. Development of interventions to assist carers of cancer patients
  6. Development of strategies to support leaders of cancer support groups

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5. Genetic counseling and testing
See Current Research Projects

With the growth of technological advances in screening for genetic disorders and the identification of increasing numbers of genetic mutations predisposing to illness, interest has grown in the impact of genetic counseling and testing, and optimal ways to communicate genetic information to individuals and families. Specific areas we have been researching include:
  1. The psychological impact of being informed one is at low, moderate or high risk, and of receiving a genetic test result (positive or negative)
  2. Impact of variations in the content and process of genetic counseling on patient outcomes.
  3. Development of a communication tool to facilitate discussions of risk

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6. End of life issues
See Current Research Projects

Many issues arise at the end of life, including communicating prognosis, referral to palliative care, and making decisions about treatment. Specific areas we have been researching include:
  1. Optimal methods to communicate about prognosis and end-of life issues, including timing, content and process issues
  2. Timing of referral to palliative care
  3. Methods to reduce pain and other symptoms at the end of life.
  4. Communicating with bereaved relatives

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