Peer Education on Core Health Outcomes Specific for Burn Patients

June 17, 2024 updated by: Heba Abubakr Mohamed Salama, Mansoura University

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

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

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed 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.

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Mansoura, Egypt
        • Heba Abubakr Salama

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Description

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 Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: control group
this group will receive the routine hospital care provided in burn center
Experimental: peer education group
this group will receive the routine hospital care, in addition to the proposed peer education by trained peer.
Patients in this group will receive the routine hospital care, in addition to the proposed peer education by trained peer

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in Burn Specific Health Scale measurements
Time Frame: 3 months
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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Ola E Elsherbiny, pHD, Mansoura University, Faculty of Nursing

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 15, 2023

Primary Completion (Actual)

May 20, 2023

Study Completion (Actual)

July 1, 2023

Study Registration Dates

First Submitted

March 2, 2023

First Submitted That Met QC Criteria

March 2, 2023

First Posted (Actual)

March 13, 2023

Study Record Updates

Last Update Posted (Actual)

June 20, 2024

Last Update Submitted That Met QC Criteria

June 17, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Peer education burn patients

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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