Clinical Trials Logo
  1. Home
  2. Burns
  3. NCT05766917
  4. Details
NCT05766917 Clinical Trial

Peer Education on Core Health Outcomes Specific for Burn Patients

Burns Clinical Trial

Official title:
Effectiveness of Peer Education on Core Health Outcomes Specific for Burn Patients: Randomized Controlled Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05766917
Other study ID # Peer education burn patients
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 15, 2023
Est. completion date July 1, 2023

Study information
Verified date June 2024
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluate the Effectiveness of Peer Education on Core Health Outcomes Specific for Burn Patients

Description:

A randomized controlled study will done in the Plastic & Reconstructive Burn Center at Mansoura University Hospitals. the first phase includes the systematic collection of data to assess patient's health status and determine any actual or potential health problems after necessary permission taken. The researcher will design the proposed peer education and educational media based on the findings of the assessment. After peers training, implementing peer education for the study group. The final step of data collection is evaluating the patient's response to the proposed program and the extent to which the outcomes have been achieved.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date July 1, 2023
Est. primary completion date May 20, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria for patients: Recently admitted patients - Hemodynamically stable and Free from chronic disease - Conscious, able to communicate Inclusion criteria for peer: - old burns injury patients at least have a diploma degree Exclusion Criteria: -

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• peer education group
Patients in this group will receive the routine hospital care, in addition to the proposed peer education by trained peer

Locations
Country Name City State
Egypt Heba Abubakr Salama Mansoura

Sponsors (1)
Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary change in Burn Specific Health Scale measurements the outcome will be measured three times (before , after intervention and after three months ) The scoring system will performed as follows: responses to each of the 40 items are rated on a five- point scale from zero (extremely) to four (not at all) for each of the 40 items. Mean scores are calculated for each domain. The maximum score was 160 points and the minimum score was 0. A higher mean score indicates more positive evaluation of patients core health outcome. 3 months
See also
  Status Clinical Trial Phase
Completed NCT05023135 - DeepView SnapShot Portable (DV-SSP): Device Training Study
Completed NCT05276869 - Reliability and Feasibility of WeeFIM Instrument to Measure Functional Independence in Pediatric Burns
Completed NCT04548635 - VR for Burn Dressing Changes at Home Phase 2/Phase 3
Not yet recruiting NCT06076031 - Effects of Applying Streaming Media on Reducing Pain in Patient With Second-degree Burn During Changing Dressing N/A
Recruiting NCT05084248 - Vitamin D Deficiency in Adults Following a Major Burn Injury Phase 4
Completed NCT03113253 - TRANexamic Acid to Reduce Bleeding in BURN Surgery Phase 4
Recruiting NCT04090424 - Assessment of Safety and Effectiveness of NovoSorb® BTM in Severe Burns N/A
Not yet recruiting NCT05649891 - Checklists Resuscitation Emergency Department N/A
Withdrawn NCT03159182 - Study of Silicone Material Inserts To Treat Burn Scars N/A
Recruiting NCT02904941 - Human Amniotic Versus Synthetic Membrane as a Transient Skin Cover for Pediatric Burns N/A
Completed NCT02681757 - Comparison of Mepitel Ag vs Antibiotic Ointment Used With Soft Cast Technique for Treatment of Pediatric Burns N/A
Recruiting NCT01812941 - Evaluation of Mitochondrial Dysfunction in Severe Burn and Trauma Patients N/A
Completed NCT01437852 - StrataGraft® Skin Tissue as an Alternative to Autografting Deep Partial-Thickness Burns Phase 1
Completed NCT01214811 - Open Multi-centre Investigation to Evaluate Signs and Symptoms of Local Inflammation/Infection on Chronic Ulcers and Partial Thickness Burns When Using Mepilex Border Ag as an Anti-microbial Wound Dressing Phase 3
Completed NCT01061502 - Efficacy Study of a Bioelectric Dressing to Treat Skin Graft Donor Site Wounds Phase 1/Phase 2
Terminated NCT00822796 - Thermogard™ Efficacy Trial N/A
Terminated NCT00824681 - Effect of Music Therapy on Families of Burn Patients Phase 1
Terminated NCT00634166 - Effects of Therapy With Sulfamylon® 5% Topical Solution Compared to a Historical Control Group Phase 4
Terminated NCT00464386 - Continuous Glucose Monitoring (POC) in the ICU N/A
Withdrawn NCT00216983 - Proline Metabolism in Severely Burned Patients: Effect of Modulated Parenteral Feeding N/A