Mobile Application Effectiveness in Pressure Injury Care

Sponsor
University of Beykent (Other)
Overall Status
Completed
CT.gov ID
NCT05255627
Collaborator
(none)
58
1
2
3
19.2

Study Details

Study Description

Brief Summary

The research was designed in a randomized controlled experimental type in order to determine the effect of mobile application on students' knowledge levels and satisfaction levels about the prevention, treatment and care of pressure injuries. The population of the study conducted in the fall semester of the 2020-2021 academic year consisted of students enrolled in the Basic Principles and Practices in Nursing course at a foundation university in Istanbul between March and June 2021 (N=78). The sample size was calculated with G power 3.1.9.4, based on similar studies, and it was calculated that at least 28 people should be included in each group, with the pre-acceptance of α error being 5%, research power (power) 80%, and an effect value of 0.77.

Research data were collected using the "Structured Description Form", "Modified Pieper Pressure Wound Knowledge Test" and "Satisfaction Scale".

Condition or Disease Intervention/Treatment Phase
  • Other: Control
  • Other: Mobile application group (Experimental Group)
N/A

Detailed Description

The research was designed in a randomized controlled experimental type in order to determine the effect of mobile application on students' knowledge levels and satisfaction levels about the prevention, treatment and care of pressure injuries.

Research Hypotheses Hypothesis 1 (H1) The knowledge level of nursing students using mobile applications in teaching the care and treatment of pressure injuries is higher than the students receiving education with the classical method.

Hypothesis 2 (H2) Nursing students who receive education using mobile applications in teaching the care and treatment of pressure injuries have higher education satisfaction levels than students who receive education with the classical method.

Universe and Sample The population of the study conducted in the fall semester of the 2020-2021 academic year consisted of students enrolled in the Basic Principles and Practices in Nursing course at a foundation university in Istanbul between March and June 2021 (N=78). Power analysis (NCSS-PASS Statistical package) was performed to determine the number of students who would form the research sample. The sample size was calculated with G power 3.1.9.4, based on similar studies, and it was calculated that at least 28 people should be included in each group, with the pre-acceptance of α error being 5%, research power (power) 80%, and an effect value of 0.77. In this direction, 58 students who met the study criteria formed the sample of the study. In the randomization of the study, students were assigned to the experimental (n=29) and control (n=29) groups according to their numbers in the class list using the www.random.org program. Research data were collected using the "Structured Description Form", "Modified Pieper Pressure Wound Knowledge Test" and "Satisfaction Scale".

Study Design

Study Type:
Interventional
Actual Enrollment :
58 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
The Effect Of The Mobıle Applıcatıon On Nursıng Students On Preventıon, Treatment And Care Of Pressure Injury
Actual Study Start Date :
Mar 15, 2021
Actual Primary Completion Date :
Mar 15, 2021
Actual Study Completion Date :
Jun 15, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Control Group

"Prevention, Care and Treatment of Pressure Injury" was explained by 1 researcher who is responsible for the Nursing Fundamentals course, using written educational material prepared in line with the literature.

Other: Control
"Prevention, Care and Treatment of Pressure Injury" was explained by 1 researcher who is responsible for the Nursing Fundamentals course, using written educational material prepared in line with the literature.

Experimental: Mobile application group (Experimental Group)

A mobile application program was installed on their phones for the experimental group students to benefit from. "Prevention, Care and Treatment of Pressure Injury" was explained by 1 researcher who is responsible for the Nursing Fundamentals course, using a mobile application program prepared in line with the literature.

Other: Mobile application group (Experimental Group)
A mobile application program was installed on the phones of the experimental group students for their benefit. "Prevention, Care and Treatment of Pressure Injury" was explained by 1 researcher who is responsible for the Nursing Fundamentals course, using a mobile application program prepared in line with the literature.

Outcome Measures

Primary Outcome Measures

  1. knowledge levels [2 Months]

    Nursing student were informed about the prevention, care and treatment of pressure injuries.

  2. Level of Satisfaction [2 Month]

    Level of Satisfaction: The satisfaction levels of nursing students from the training given about the prevention, care and treatment of pressure injury were determined.

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years to 22 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Nursing students;

  • be 18 years or older,

  • Not having graduated from Health Vocational High School,

  • To be registered for the first time in the Basic Principles and Practices in Nursing course, to fully participate in the interventions to be applied in the study.

  • Volunteer to participate in the study.

Exclusion Criteria:

Nursing students;

  • be under the age of 18,

  • Having graduated from Health Vocational High School,

  • Having taken the Basic Principles and Practices in Nursing course before,

  • Not participating in the initiatives to be implemented in the study,

  • Not willing to participate in the study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Beykent University Istanbul Beykent Turkey 34500

Sponsors and Collaborators

  • University of Beykent

Investigators

  • Principal Investigator: Hamiyet Kızıl, PhD RN, Beykent University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Hamiyet KIZIL, PhD RN Assistant Professor Hamiyet KIZIL, University of Beykent
ClinicalTrials.gov Identifier:
NCT05255627
Other Study ID Numbers:
  • 15032021
First Posted:
Feb 24, 2022
Last Update Posted:
Feb 24, 2022
Last Verified:
Feb 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 Hamiyet KIZIL, PhD RN Assistant Professor Hamiyet KIZIL, University of Beykent
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 24, 2022