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Education Program for Burn Patients

Not Applicable
Completed
Conditions
Burns
Interventions
Behavioral: educational program+telephone follow up
Registration Number
NCT01379495
Lead Sponsor
University of Sao Paulo
Brief Summary

The purpose of this study is to assess the effect of an educative program including telephone follow-up for burn patients regarding the impact of this intervention on the health status and return to work at six months after hospital discharge.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
83
Inclusion Criteria
  • adult burned patients (18 years or older), male and female
  • patients burned for the first time who needed hospitalization at the Burns Unit
  • in cognitive conditions to participate (being able to tell one's address, day of the week and age or birth date)
  • in physical conditions to accomplish self-care.
Exclusion Criteria
  • participants burned due to suicide or with previous psychiatric diagnoses or cognitive and psychological difficulties that do not allow them to answer the instrument questions and take care of themselves.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
educational program+telephone follow upeducational program+telephone follow upBurns victims will participate in an educative program including telephone follow-up during six months after hospital discharge
Primary Outcome Measures
NameTimeMethod
change from baseline in perceived health status at six monthssix months

The questionnaire "Burns Specific Health Scale- Revised" developed by Blalock; Bunker; De Vellis (1994), adapted by Ferreira et al. (2008) to Brasilian people, will be used to collect the data at six months between groups.

Secondary Outcome Measures
NameTimeMethod
comparison the return to work of burn victims between groupsbaseline and six months

To compare the return to work of burns victims in intervention group with the return to work of burns victims in control group at six months after hospital discharge, proportions will be calculated (returned to work: yes/no)

Trial Locations

Locations (1)

Burns Unit of the University of São Paulo at Ribeirão Preto Hospital das Clínicas

🇧🇷

Ribeirão Preto, São Paulo, Brazil

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