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

G

Gazi University

Status

Not yet enrolling

Conditions

Childhood Cancer

Treatments

Other: Well-Being Process Program (WEBEPROP)

Study type

Interventional

Funder types

Other

Identifiers

NCT05457153
2021 - 846

Details and patient eligibility

About

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".

Full 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.

Enrollment

60 estimated patients

Sex

All

Ages

10 to 20 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Between the ages of 10-20,
  • Child and adolescent with palliative care needs
  • At least 3 months before diagnosis
  • Child and adoescent have completed the induction phase of treatment,
  • İntermediate-high-risk group defined under a treatment protocol,
  • Child and aolescent can utilizecomputer, mobile phone and tablet
  • Children and adolescents who agreed to participate in the survey and their parent.

Exclusion criteria

  • Newly diagnosed with physical and mental disabilities,
  • Child and adolescent with severe anxiety according to the anxiety score scale,
  • Out of diagnosis in the last 6 months (loss of parents, natural disaster, etc.) are children and adolescents who experience high levels of stress and have an important psychiatric diagnosis that affects their mental health.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Technology-Based Well-Being Process Program
Experimental group
Description:
WEBEPROP will be conducted for 8 weeks. The program for the intervention group is included the modüls. In the program, the modules of "Self-Knowledge, Inner Communication and Awareness of Perceptions, Emotion and Thought Management" will be completed in 8 weeks (each model two weeks) . The other module will not be accessible and cannot be switched before the prevous module is completed.
Treatment:
Other: Well-Being Process Program (WEBEPROP)
Control Group
Active Comparator group
Description:
After the first follow-ups have been made to the control group, they will continue to receive standard care. After the monitoring of the initiative group within the scope of the program is completed, the website of the well-being process program will be made available to the control group. Children and adolescents will benefit from the modules by promoting the website.
Treatment:
Other: Well-Being Process Program (WEBEPROP)

Trial contacts and locations

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Central trial contact

Ebru KILIÇARSLAN TORUNER,, PhD, RN; Sümeyye YILDIZ, PhD Student

Data sourced from clinicaltrials.gov

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