NCT05707624

Brief Summary

Aim: The study was carried out to evaluate the effect of distance education, which is given with a video prepared for the approach to the child with fever, on the knowledge, attitudes and behaviors of parents with children in the 0-5 age group. Method: This is a randomized controlled intervention study. The research was carried out in Eskişehir City Hospital Pediatric Emergency Service, between 8th April 2022 and 10th June 2022. The study was completed with 99 parents with children aged 0-5 years old who consulted to the pediatric emergency service with the complaint of fever. In the study, there are 2 groups in total: the intervention group (n=50) which videos of approaching the febrile child was watched once a week and 2 videos, and the control group (n=49) which no other application is made except for the routine procedure of the hospital. "Descriptive Information Form" and "Parental Fever Management Scale" were used to collect data. Data collection tools were applied to the parents before and after the application. IBM SPSS Statistics 26 package program was used to evaluate the data. A statistically significant p\<0.05 value was accepted.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
99

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2020

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 14, 2020

Completed
2.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 25, 2022

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

December 26, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 26, 2022

Completed
1 month until next milestone

First Posted

Study publicly available on registry

February 1, 2023

Completed
Last Updated

February 1, 2023

Status Verified

January 1, 2023

Enrollment Period

2.4 years

First QC Date

December 26, 2022

Last Update Submit

January 21, 2023

Conditions

Outcome Measures

Primary Outcomes (2)

  • descriptive information form

    This form measures participants knowledge, attitude and behaviours about fever in 0-5 ages children. After intervention, it is expected that; The intervention group which was given remote video training for fever, had a higher level of knowledge and positive attitudes and behaviours about fever than the control group, where the routine procedure of the hospital was applied.

    2 months

  • Parent fever management scale

    This scale measures patients fever management for their children. It shows that parents have more fever anxiety and perform more fever management when the scale scores are high. After intervention, it is expected that; The Parental Fever Management Scale scores of the intervention group given remote video training for fever were lower than the control group in which the routine procedure of the hospital was applied.

    2 months

Study Arms (2)

experimental

EXPERIMENTAL

During the process; Phone numbers were obtained and recorded at the first meeting with the parents. The link of the first two training videos was sent to the smartphones of the participants at the same time. Parents are explained how to access the videos from the link. Afterwards, other training videos, prepared once a week and as 2 videos, were sent to the parents' smartphones on a regular basis. After the procedure; Participants were contacted by phone 2 weeks after the last videos were watched. They were asked to fill out and send the questionnaire and scale online sent to their phones.

Other: video education

Control group

PLACEBO COMPARATOR

During the process; The phone number obtained from the parents was recorded and no other application was made other than the routine procedure of the clinic. Parents were not contacted in the following weeks. After the procedure; The control group was also reached via telephone 2 weeks after the video submission to the intervention group was completed. They were asked to fill out and send the questionnaire and scale online sent to their phones.

Other: the routine procedure

Interventions

In the study, there are 2 groups in total: the intervention group (n=50) which videos of approaching the febrile child was watched once a week and 2 videos, and the control group (n=49) which no other application is made except for the routine procedure of the hospital

experimental

the routine procedure

Control group

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • The parent brought the child to the emergency room with a complaint of fever,
  • The child is between 0-5 years old,
  • Parent's consent to participate in the study,
  • Parent's ability to read and write,
  • Parent's ability to understand and speak Turkish,
  • Parent has a smartphone to watch videos.

You may not qualify if:

  • If the parent has a disability that will prevent them from participating in the training (For example, having a hearing impairment, etc.)
  • The age of the child is over 5 years old.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Eskisehir Osmangazi University

Eskişehir, Tepebasi, 26200, Turkey (Türkiye)

Location

Related Publications (1)

  • Toksoz F, Acikgoz A. Randomized controlled study: The effect of video-based distance education for approaching children with fever on parents' knowledge levels and fever management. J Pediatr Nurs. 2024 May-Jun;76:e42-e49. doi: 10.1016/j.pedn.2024.01.017. Epub 2024 Jan 25.

MeSH Terms

Conditions

Fever

Condition Hierarchy (Ancestors)

Body Temperature ChangesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • fatma Toksoz

    Eskisehir Osmangazi University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: Simple random sampling method was used in the study. Parents who met the research inclusion criteria were assigned to the groups by drawing lots. In the lottery method, first of all, the control and intervention groups were written by the researcher on 1st paste and 80 g/m2 A4 papers of 4x4 cm size and the papers were placed in a bag that is invisible. Then, when the first parent who met the criteria for inclusion in the emergency room came, any nurse working in the service other than the researcher was asked to choose a paper from the bag (by blinding). If a control group is written on the paper, it is assigned to the parent control group, and if it is written as an intervention group, it is assigned to the parent intervention group. When the second parent who met the criteria for inclusion in the emergency department came, lots were not drawn, and the parent was assigned to the other group. The same procedure was repeated for all subsequent participants.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant

Study Record Dates

First Submitted

December 26, 2022

First Posted

February 1, 2023

Study Start

July 14, 2020

Primary Completion

December 25, 2022

Study Completion

December 26, 2022

Last Updated

February 1, 2023

Record last verified: 2023-01

Data Sharing

IPD Sharing
Will not share

Locations