Cancer, Sleep disorder, Circadian rhythm disorder
Conditions
Interventions
Subjects will be received following two interventions for three days. 1.Recording the time of breakthrough pain and the degree of pain (NRS). 2.Measuring circadian rhythm related factors (actigraph,
s hospital sleep questionnaire, urine 6-sulfatoxymelatonin and so on). In addition, assessment anxiety and depression by HAD at getting informed consent.
Sponsors
Osaka University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Cancer patients without changing opioid medication for more than three days.
Exclusion criteria
Exclusion criteria: Cancer patients with heavy dementia, <= PS2, on anticancer drug medicaton.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The relationship between breakthrough pain and circadian rhythm related factors | — |
Countries
Japan
Contacts
Public ContactKazuyuki NIki
Osaka University/Ashiya Municipal Hospital Graduate School of Pharmaceutical Sciences/Department of Pharmacy
Outcome results
None listed