Simulation-Based Training on the Preparedness and Burden of Caregiver

Sponsor
Hacettepe University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04745208
Collaborator
The Scientific and Technological Research Council of Turkey (Other)
40
1
2
13.6
2.9

Study Details

Study Description

Brief Summary

Major burn injuries are serious traumas that cause physical and psychological problems. The acute period that begins with admission to the hospital is followed by a rehabilitation period that lasts for months or even years. The main goal in the acute care of the patient in hospital is to discharge the patient from the hospital as soon as possible, with the least morbidity, functional and cosmetic loss. The care of the patient in rehabilitation period continues at home, and the home care is provided by informal caregivers. Due to the physiological and psychological changes occurring in the patient with burns, the informal caregiver has important duties such as; helping with or doing feeding, wound care, personal care, organizing household chores, providing economic, medical and psychological support. So that, informal caregivers may experience lack of information and anxiety. Nurses should include the informal caregivers in discharge education to meet the information requirement of them, to prepare them for home care and to reduce anxiety of home care. The basis of discharge education is to help individual to cope with the problems related to the disease and to maintain individual care. Nurses, who play a key role in discharge education, have been keeping up with the change over the years and trying to maintain the effectiveness of education by various methods. The educational environment enriched with different technological tools and materials used in the field of education makes it easier to provide a change of behavior in the desired direction in the learner. A controlled and safe simulation environment ensures patient safety at all times, while ensuring that training is tailored specifically to the needs of the trained. Simulation gives caregivers an opportunity to manage stressful medical events in a risk-free environment, which allows healthcare providers to be involved in and manage the family's traditional education when it comes to caring and teaching families. When the literature on increasing the preparedness of the caregivers for care, and thus reducing the burden of care, no studies evaluating the simulation-based training for informal caregivers were found. This study was needed with the idea that simulation-based training, which is provided with a high fidelity of moulage, will help the caregiver to understand the burn care easily, to be ready for care and therefore to reduce the burden of care.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Simulation based education
N/A

Detailed Description

Method:

The study was designed as a randomised controlled study with the control group in order to determine the effect of simulation-based training applied to the caregivers of burn patients on their preparedness for care and caregiving burden. The research will be conducted in the Burn Unit of Hacettepe University Adult Hospital and Burn Center of Gulhane Training and Research Hospital. The population of the research includes caregivers of adult patients admitted to Hacettepe University Adult Hospital Burn Unit and Burn Center of Gulhane Training and Research Hospital after 02.02.2021 and have treatment in inpatient or outpatient clinics. Since there is no similar research in the literature, sample size was not calculated. At the end of the study, power analysis will be done to evaluate the adequacy of the sample size. In the study, participants in the intervention group and control group will be assigned by block randomization method and each block will consist of 4 caregivers and 6 blocks will be formed. The data sheets of the research are Caregivers Information Form, Preparedness for Caregiving Scale, Caregiving Burden Scale and Post-Discharge Assessment Form for Burn patients. In addition, the Questionnaire for the Burn patients will be used to obtain information about the burn patients.

Implementation of study:

The control group will receive only the standard discharge education. Simulation based education will be performed after the standard discharge training with the intervention group. The preparedness of caregivers before and after both training will be assessed. The burden of caregiving will be assessed during the first and third months of care.

Collection of Data:

In order to test the understandability of standard discharge training, training will be provided to 3 patient relatives. The presentation of the training will be organized according to the feedback received.

After the pre-application of the simulation scenario in the laboratory environment 3 times, the necessary changes will be made on the scenario and the final version will be given.

Data collection tools will be applied on the both group, unrecognized questions and corrections will be made on missing items. Individuals participating in these preliminary studies will not be included in the study.

Percentage, mean, standard deviation will be used in the evaluation of the data. Chi-square, Fisher's exact test, independent paired T-test and Mann-Whitney U test will be used for comparison between groups and within groups. p <0.05 will be considered statistically significant.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Simulation-based education will be performed after the standard discharge training with the intervention group. The control group will receive only the standard discharge educationSimulation-based education will be performed after the standard discharge training with the intervention group. The control group will receive only the standard discharge education
Masking:
Single (Outcomes Assessor)
Masking Description:
Outcome assessor will be masked in the clinical trial. One of the investigators will enter the data by giving "a" for control group and "b" for intervention group. So that, the outcome assessor will not have knowledge which group is exposed to intervention.
Primary Purpose:
Other
Official Title:
The Effect of Simulation-Based Training on the Preparedness and Burden of Caregiver of Patients With Burns: A Randomised Controlled Study
Actual Study Start Date :
Mar 13, 2021
Anticipated Primary Completion Date :
Mar 22, 2022
Anticipated Study Completion Date :
Apr 30, 2022

Arms and Interventions

Arm Intervention/Treatment
No Intervention: standard discharge education

The control group will receive only the standard discharge education.

Experimental: standard discharge education+Simulation based education

The intervention group will receive standard discharge education and then simulation based education will be performed

Behavioral: Simulation based education
high fidelity simulation with moulage

Outcome Measures

Primary Outcome Measures

  1. caregiving burden [from first month until third month]

    The caregiver burden score will be assessed by Burden Scale for Family Caregivers.

  2. Preparedness of care [First assessment at time of acceptance of the study -2 day after education]

    The readiness of caregiving will be assessed at the time of acceptence and post-training education by Preparedness for Caregiving Scale.

Secondary Outcome Measures

  1. Burn Patient Fallow Up [3 months]

    Burn patients will be fallowed from through 3 months and complications, rehospitalizations number, etc. will be recorded.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Caring for patients with burn during the study

  • Being over 18 years old

  • Agree to participate voluntarily in the study

  • To communicate

  • Not having a diagnosed mental problem

  • The burn patient he/she cares for is over the age of 18, inpatient treatment in the burn unit, no communication problem, no diagnosed mental problem, no additional problem (fracture, paralysis, etc.) except burn.

  • At least 5 days to be discharged from the burns patient,

  • Not being a healthcare professional

  • Not caring for another family member, except burn patients.

Exclusion Criteria:
  • Loss of life of the burned individual and/or caregiver during the study.

  • The participant declares that he/she wants to leave at any stage of the study.

  • Not participating in data collection in the first and third months.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hacettepe University Ankara Turkey 06100

Sponsors and Collaborators

  • Hacettepe University
  • The Scientific and Technological Research Council of Turkey

Investigators

  • Principal Investigator: Zahide Tuncbilek, Asst. Prof., Hacettepe University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Sabri Karahan, Principal Investigator, Hacettepe University
ClinicalTrials.gov Identifier:
NCT04745208
Other Study ID Numbers:
  • KA-19021
First Posted:
Feb 9, 2021
Last Update Posted:
Mar 4, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sabri Karahan, Principal Investigator, Hacettepe University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 4, 2022