Patients with skin implants
Conditions
Interventions
If Monday is the surgery day, Group A will use the normal lower limb trestle from Tuesday after extubation to the third postoperative day, and from Friday afternoon of the fourth day, a lower limb tre
Sponsors
Tokushima University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients: Patients who have undergone skin grafting and whose attending physicians determine that they are eligible for the study will be included. The patients will be assigned a number when they agree to cooperate in the study. This will be a randomized controlled trial, with odd numbers assigned to group A and even numbers assigned to group B. The study will be conducted on three days during the six-day postoperative period, one day using the new wool mat wrapped lower limb trestle and three days using the conventional lower limb trestle, so that eligible patients will experience both types of lower limb trestles. Nurses: Nurses who were engaged in care (patient observation and nursing activities including daily ward duties such as blood pressure monitoring and wiping) during the study period.
Exclusion criteria
Exclusion criteria: Patients: Exclusion criteria will be patients deemed inappropriate by the attending physician and those who have developed skin problems, are in severe mental or physical distress, or whose consent could not be obtained. Nurses: Those for whom consent could not be obtained.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Questionnaires and Interviews with Patients Questionnaire for nurses | — |
Countries
Japan
Contacts
Public Contactyoshie IMAI
Tokushima University Cancer nursing
Outcome results
None listed