Actively Recruiting
The Effect of Mandala on Anxiety and Fear Levels in Children With Leukemia Before Intrathecal Chemotherapy Treatment
Led by Ege University · Updated on 2026-02-17
60
Participants Needed
1
Research Sites
48 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to examine the effect of mandala coloring activity, administered before intrathecal chemotherapy treatment in children with leukemia, on pre-procedure anxiety and fear in children. The main question this study aims to answer is: Does mandala coloring administered before intrathecal chemotherapy treatment reduce pre-procedure anxiety and fear in children with leukemia? Descriptive demographic data will be collected from the children who will be given mandalas. Data will be collected using an Anxiety Scale and a Fear Scale.
CONDITIONS
Official Title
The Effect of Mandala on Anxiety and Fear Levels in Children With Leukemia Before Intrathecal Chemotherapy Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- The patient must be between 4 and 12 years of age.
- The patient must be hospitalized and followed up at the Pediatric Hematology Clinic.
- The patient must only be receiving leukemia treatment.
- The patient must not have any other chronic diseases.
- The patient must not have any systemic infections.
- The patient has received at least two courses of intrathecal chemotherapy treatment.
- The patient does not have a diagnosis of psychological or mental symptoms as a side effect of chemotherapy treatment.
- Intrathecal treatment will be administered to the patient according to the chemotherapy protocol.
- The patient and the caregiver parent are volunteers.
- The caregiver parent speaks Turkish and is open to communication.
You will not qualify if you...
- Cases that do not meet the inclusion criteria will be excluded from the study.
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Trial Site Locations
Total: 1 location
1
Ege University Childrens Hospital
Izmir, Turkey (Türkiye)
Actively Recruiting
Research Team
S
Seda ARDAHAN SEVGİLİ, Ph.D
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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