This study targets pediatric and adolescent cancer patients who are in the
acute-transitional survival period(during cancer treatment to within 2 years of treatment
end date) and their primary caregivers. Evaluation on the cognitive and psycho-social
functions of pediatric and adolescent patients and their primary caregivers are conducted
beforehand. Subsequently, the patients and caregivers are provided with psycho-education
and psychological intervention program developed by the research team. The program is
provided on a 1:1 basis to each subject to verify its effectiveness in improving quality
of life, including mental health.
For patients and caregivers starting or undergoing cancer treatment, the purpose and
information of the study will be informed when they visit the research participating
institution: National Cancer Center or Seoul National University Hospital. For patients
and caregivers who have completed the cancer treatment and the treatment end date is
within 2 years, the research team will screen the patients during the relevant period.
The purpose and information of the study will be provided during outpatient treatment.
The research involves vulnerable subjects such as minors, therefore under the consent of
the caregiver(a legal guardian), consent form with age-appropriate explanations of the
study will be provided.
Before beginning the session, the patients will carry out neurocognitive assessments. The
assessments includes Intelligence (Korean Wechsler Intelligence Scale for Children 4th
and 5th Edition/Korean Wechsler Intelligence Scale 4th Edition), Memory(Rey-Kim Memory
Test), Executive Function(Kims Frontal-Executive Neuropsychological Test),
Attention(Children's Color Trails Test, Advanced Test of Attention / Trail Making Test,
Continuous Performance Test), and Visual-Motor Integration 6th Edition.
During the pre-evaluation and orientation session, a counseling structure is establish
for the next sessions of the program. The psycho-education and psychological intervention
program is developed by comprehensively reflecting patient and caregiver interviews,
previous research, and research team opinions. The program integrates and applies various
evidence based theories, such as mindfulness theory, solution-focused theory, resilience
theory, and family intervention theory. Consisting of core modules and elective modules,
the program varies whether the patient is starting or undergoing cancer treatment, or
have completed the cancer treatment. For patients and caregivers starting or undergoing
cancer treatment, 4 core sessions and 1 elective session(selected out of the provided 3
topics) will be conducted. For patients and caregivers whose treatment end date is within
2 years, 7 core sessions and 3 elective sessions will be conducted. Every session is a
1:1 basis except for the family session, which the patient and the caregiver will
participate together. Each session will last approximately 40-50 minutes, and conducted
1-2 times a week. The psycho-education and psychological intervention program is provided
by the participating research institution and research team who have participated in the
development of the program: National Cancer Center, Seoul National University Hospital,
and Tree and Forest Psychological Counseling Center. Each of the institution has an
assigned clinical psychologist who will conduct the sessions of the program. The program
can be conducted in person or remotely. For patients starting or undergoing treatment, an
independent counseling room will be provided by the research participating institution
conducting the cancer treatment. For those who live far away or have difficulty in
traveling to participate the program, an online video platform (ZOOM) can be utilized, or
the sessions can be conducted on an individual location requested by the research subject
under agreement.
To verify the effectiveness of the program, the patients and caregivers will carry out
psychological questionnaires 2~3 times, depending on the group they are randomized in.
For patients and caregivers starting or undergoing treatment and randomized into
experimental group(Experimental Group_In cancer treatment) will carry out the
questionnaires 2 times: before beginning the session, and after the core session(4th
session). For patients and caregivers starting or undergoing treatment but randomized
into control group(Control Group_In cancer treatment) will also carry out the
questionnaires 2 times: after enrollment, and 4 weeks after the enrollment. For patients
and caregivers whose treatment end date is within 2 years and randomized into
experimental group(Experimental Group_After cancer treatment) will carry out the
questionnaires 3 times: before beginning the session, after the core session(7th
session), and after the end of the whole session(10th session). For patients and
caregivers whose treatment end date is within 2 years but randomized into control
group(Control Group_After cancer treatment) will also carry out the questionnaires 3
times: after enrollment, 7 weeks after the enrollment, and 10 weeks after the enrollment.
