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Technology-Based Well-Being Process Program (WEBEPROP) for Children and Adolescents in Palliative Care

Childhood Cancer Clinical Trial

Official title:
Intervention Protocol: Evaluation of the Effectiveness of the Technology-Based Well-Being Process Program (WEBEPROP) for Children and Adolescents in Palliative Care: A Randomized Trial

Clinical Trial Summary

Objective: The research was planned to evaluate the effectiveness of the 8-week technology-based Well-Being Process program for children and adolescents in the palliative care period. Methods: This study was planned as a randomized controlled experimental study. The research will be carried out with children aged 12-20 years with a diagnosis of cancer, in the pediatric oncology and hematology clinics of two hospitals in Turkey. Data collection will consist of the children and adolescent's and parents' descriptive characteristic form Adolescent Spiritual Well-Being Scale, Beck Anxiety Scale, Pediatric Cancer Coping Scale and Technology-Based Spiritual Care Program Process Evaluation Forms. The program will be implemented for the intervention group. In the 8-week program; a) 4 web-based modules, b) 8 online individual interviews after each module (8 total interviews with each child) c) simultaneous mobile messages with the modules, and d) 24/7 counseling. Animation videos, breathing and progressive relaxation exercises, and imagination methods will be included in the modules. This research is based on the "Watson Model of Human Care".

Clinical Trial Description

Hypothesis: H1: There is a significant difference between the spiritual well being score averages of children and adolescents who have been administered and have not been administered WEBEPROP. H2: There is a significant difference between the anxiety scores of children and adolescents who have been administered and have not been administered WEBEPROP. H3: There is a significant difference between the coping scores of children and adolescents who have been administered and have not been administered WEBEPROP. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05457153
Study type Interventional
Source Gazi University
Contact Sümeyye YILDIZ, PhD Student
Phone 0534 682 37 94
Email sumeyye.yildiz1@gazi.edu.tr
Status Not yet recruiting
Phase N/A
Start date October 1, 2022
Completion date September 30, 2024
View Details
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