Assessment of Sleep Quality and Mobilization Using the Actigraph in Postoperative Patients with Esophageal Cancer: A Prospective Observational Study
Not Applicable
- Conditions
- Esophageal Cancer
- Registration Number
- JPRN-UMIN000051517
- Lead Sponsor
- Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Department of Anesthesiology and Resuscitology.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patients who have difficulty wearing the Actigraph on their wrist for any reason (e.g., skin abnormalities). 2. Patients who have difficulty in answering the questionnaire in Japanese. 3. Patients who are currently participating in another prospective study and have been determined to have a potential impact on each other's study results. 4. patients who are deemed inappropriate as research subjects by the principal investigator or sub investigator.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative score of The Richards-Campbell Sleep Questionnaire (RCSQ) for 4 postoperative days.
- Secondary Outcome Measures
Name Time Method umerical rating score of pain CAM-ICU for 4 potoperative days Length of ICU stay Postoperative use of analgesics Postoperative complications Start date of postoperative mobilization Parameters obtained by Actigraph for 14 postoperative days Assessment of Quality of life using EQ-5D-5