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Assessment of Sleep Quality and Mobilization Using the Actigraph in Postoperative Patients with Esophageal Cancer: A Prospective Observational Study

Assessment of Sleep Quality and Mobilization Using the Actigraph in Postoperative Patients with Esophageal Cancer: A Prospective Observational Study - ACT study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000051517
Enrollment
20
Registered
2023-07-04
Start date
2023-07-10
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal Cancer

Interventions

None listed

Sponsors

Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Department of Anesthesiology and Resuscitology.
Lead Sponsor
Okayama University Graduate School of Interdisciplinary Science and Engineering in Health Systems, Department of Biomedical Informatics. Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Department of Gastroenterological Surgery.
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients scheduled for radical esophagectomy. 2. Patients who are 18 years old or older. 3. Patients who are able to obtain written consent for research participation of their own free will.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
Postoperative score of The Richards-Campbell Sleep Questionnaire (RCSQ) for 4 postoperative days.

Secondary

MeasureTime frame
Numerical 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-5L

Countries

Japan

Contacts

Public ContactYoshikazu Kimura

Okayama university Okayama University Hospital, Anesthesiology and resuscitology

yoshikimura_16@yahoo.co.jp086-235-7778

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026