Patients with chronic pain
Conditions
Interventions
None listed
Sponsors
Yamaguchi University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patients who have been suffering from chronic pain for more than 3 months at the time of obtaining consent 2) Patients who are 18 years of age or older at the time of obtaining consent 3) Gender irrelevant 4) Patients who have received a sufficient explanation of their participation in this study, fully understood the information, and voluntarily provided written consent
Exclusion criteria
Exclusion criteria: 1) Patients whose pain intensity was less than 3 on the Numerical Rating Scale (NRS) at the examination on the day of consent acquisition. 2) Patients with psychiatric disorders that have a clear impact on pain and sleep. 3) Patients with irregular sleep habits due to their occupation (e.g., three-shift work). 4) Patients who work in jobs that do not allow them to wear an actigraph during the day (e.g., cleaning operations, civil engineering work). 5) Patients who are unable to keep a sleep diary. 6) Patients who are otherwise deemed inappropriate as study subjects by the principal investigator (co-investigator).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Bidirectional relationship between pain intensity and sleep parameters | — |
Secondary
| Measure | Time frame |
|---|---|
| Sleep satisfaction, sleep efficiency, sleep onset latency, total sleep time, wake time after sleep onset | — |
Countries
Japan
Contacts
Public ContactHidenori Harada
Yamaguchi University Graduate School of Medicine Department of Anesthesiology
Outcome results
None listed