This study is looking at treating cancer pain in head and neck cancer. Patients are asked in outpatients to score their worst pain on a scale of 0 to 10 in the last 24 hours. Those with a pain score of 4 and above are randomised into the study. Patients are allocated to continue with their current care (control group) or to be reviewed by the pain/palliative care team (intervention group). At baseline questionnaires are completed on level of pain, type of pain, quality of life and anxiety/depression. Information is also collected on the analgesia they've used in the past month and basic health economics (GP/hospital visits related to pain management and treatment). Follow up in the trial is for 3 months and consists of questionnaires as above and further collection of information on analgesic usage and health economics.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Enrollment
156
Patients allocated to the "intervention group" will undergo prospective, proactive, integrated, structured pain treatment according to recent guidelines on cancer pain care
Royal Marsden Hospital
London, United Kingdom
The change in pain score summarized from patient reports
Time frame: 1 month, 2 months and 3 months
Impact of pain
Measured by the brief pain inventory questionnaire
Time frame: 1 month, 2 months, 3 months
Adequacy of pain treatment
Using Pain Management Index, calculated from BPI and WHO ladder
Time frame: 1 month, 2 months and 3 months
Quality of life
Assessed using the EQ-5D questionnaire
Time frame: 1 month, 2 months and 3 months
Patient satisfaction
Likert scale
Time frame: 1 month, 2 months and 3 months
Anxiety and depression
Assessed using the Hospital anxiety and depression questionnaire
Time frame: 1 month, 2 months and 3 months
Treatment costs
Information collected on analgesic usage and contact with healthcare professionals for pain management purposes
Time frame: 1 month, 2 months and 3 months
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