cancer
Conditions
Interventions
Interventional period: Postoperative, 6 months postoperative Intervention: To wear a wearable device (OMRON Active style Pro 750C) on clothing for more than a week.
Sponsors
Keio University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1:Cases pathologically diagnosed with endometrial cancer 2:From the date of approval by the Ethics Committee, patients who underwent surgery including total hysterectomy as the initial treatment for endometrial cancer at Keio University Hospital Gynecology 3:Cases over 20 years old 4:Cases with a preoperative performance status of 0 5:Cases that can be explained and understood in writing and signed with consent 6:Be able to prepare a smartphone and an email address.
Exclusion criteria
Exclusion criteria: 1:Cases with active double cancer 2:Cases with a history of cancer within 5 years other than carcinoma in situ 3:Cases with a history of serious mental illness or complications 4:Cases with a history of limb deficiency (congenital or acquired), cerebrovascular disease, and progressive neuromuscular disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation period: Postoperative, 6 months postoperative Outcome: steps per day | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation period: Postoperative, 6 months postoperative, Outcomes: 1:Grip strength 2:Sit to Stand-5 3:Health-related quality of life scale (The European Organization for Research and Treatment of Cancer QLQ-C30) 4:Ovarian deficiency symptom scale (the Keio Questionnaire) 5:Physical activity scale (international standardized physical activity questionnaire) | — |
Countries
Japan
Contacts
Public ContactKiriko Abe
Keio University school of medicine Rehabilitation medicine
Outcome results
None listed