Diabetes Mellitus
Conditions
Interventions
This is an experimental study of the randomized clinical trial type. It will be developed in the city of Recife-PE, data collection will take place in two hospital units: 1) Hospital Agamenon Magalhãe
2) Have an amputation due to diabetic complications
3) Being treated in the inpatient units of the hospitals participating in the study. Exclusion criteria: 1) Patients admitted to the Intensive Care Unit
2) Present a medical diagnosis of neurological deficit that hinders the learning process
3) Have a hearing and/or visual impairment
4) Health professionals. The sample should consist of two groups containing 98 people in each group. The recruitment of participants will occur through the identification of patients hospitalized in t
E02.760.611 N02.421.533
Sponsors
Universidade Estadual da Paraíba - UEPB
Universidade de Pernambuco - UPE
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Be 18 years of age or older; present amputation due to diabetic complications; being treated in the inpatient units of the hospitals participating in the study
Exclusion criteria
Exclusion criteria: Patients admitted to the Intensive Care Unit; presenting a medical diagnosis of neurological deficit that hinders the learning process; have hearing and/or visual impairment; Health professionals
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find a reduction in the length of stay, a decrease in the rate of complications such as: reinfections and readamputations, through the application of the protocol and the data collection instrument that includes the records of the length of stay and subsequent complications identified through the measurement /record of hospitalization days, number of reinfections and reamputations | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to verify the reduction or relief of pain reports, through the evaluation of pain on a numerical scale contained in the protocol;Reduce healing time by applying the protocol, in addition to measuring healing time based on the number of days between the onset of injury and healing;Identify motor difficulties and provide guidance to achieve the highest possible level of autonomy through the Barthel Index, which verifies functional independence through scoring according to the questions, and indicates the possibility of carrying out daily activities, the lower the score, the lower the functional capacity of the patient to perform the activities;Identify the rates of glycemic curve control, through capillary blood glucose and recording in a data collection instrument through measurement with capillary blood glucose values | — |
Countries
Brazil
Contacts
Public ContactNalva Lima
Universidade Estadual da Paraíba - UEPB
Outcome results
None listed