F Boyle
Biographic Data
| ID | 3934520 |
|---|---|
| NAME | F Boyle |
| GIVEN NAMES | F |
| FAMILY NAME | Boyle |
| SIGNATURE | BOYLE F |
| AFFILIATIONS | Royal North Shore Hospital |
| VERIFIED | No |
| TOTAL WORKS | 3 |
| TOTAL CITATIONS | 7 |
| AUTHOR COUNT | 3 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2004 |
| LATEST PUBLICATION YEAR | 2015 |
| H-INDEX | 1 |
Can consultation skills training change doctors' behaviour to increase involvement of patients in making decisions about standard treatment and clinical trials
BACKGROUND: Informed consent is required for both standard cancer treatments and experimental cancer treatments in a clinical trial. Effective and sensitive physician-patient communication about informed consent is difficult to achieve. Our aim was to train doctors in clear, collaborative and ethical communication about informed consent and evaluate the impact of training on doctor behaviour, stress and satisfaction. PARTICIPANTS AND METHODS: Par…
Improving informed consent
Background Patients and clinicians report difficulties with the process of informed consent to clinical trials and audiotape audits show that critical information is often omitted or poorly presented. Decision aids (DAs) may assist in improving consent. Aims This study piloted a DA booklet for a high priority breast cancer prevention trial, IBIS‐II DCIS, which compares the efficacy of an aromatase inhibitor (anastrozole) with tamoxifen in women w…
Seeking informed consent to cancer clinical trials
Seeking informed consent to cancer clinical trials
Improving informed consent
Background Patients and clinicians report difficulties with the process of informed consent to clinical trials and audiotape audits show that critical information is often omitted or poorly presented. Decision aids (DAs) may assist in improving consent. Aims This study piloted a DA booklet for a high priority breast cancer prevention trial, IBIS‐II DCIS, which compares the efficacy of an aromatase inhibitor (anastrozole) with tamoxifen in women w…
Can consultation skills training change doctors' behaviour to increase involvement of patients in making decisions about standard treatment and clinical trials
BACKGROUND: Informed consent is required for both standard cancer treatments and experimental cancer treatments in a clinical trial. Effective and sensitive physician-patient communication about informed consent is difficult to achieve. Our aim was to train doctors in clear, collaborative and ethical communication about informed consent and evaluate the impact of training on doctor behaviour, stress and satisfaction. PARTICIPANTS AND METHODS: Par…
Alternative medicine (3 works) · Clinical trial (3 works) · Ethics in Clinical Research (3 works) · Family medicine (3 works) · Informed consent (3 works) · Medicine (3 works) · Patient-Provider Communication in Healthcare (3 works) · Medical education (2 works) · Randomized controlled trial (2 works) · Blinding (1 works)