NCT06969742Recruiting
Development and Application of Intervention Program to Improve Mental Health and Quality of Life of Solid Tumor Survivors and Caregivers
Development and Clinical Application of Intervention Program to Improve Mental Health and Quality of Life of Pediatric Solid Tumor Survivors and Caregivers, a Multicenter, Experimental Group, Pre-and-post Evaluation Intervention Study
Source: ClinicalTrials.gov · Last updated 14 May 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The research team will assess the psychological abilities like cognitive(how you think and figure things out) and psycho-social(the well-being at the intersection of the internal workings and external experience) functions of young patients who are diagnosed with solid tumor and their primary caregivers. After assessing the psychological abilities, the research team will provide counseling and educational sessions developed by the team. The sessions are provided on a 1:1 basis to each of the participants to verify whether the sessions helped to improve the quality of life, including mental health.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 120 (estimated)
- First submitted
- 10 Mar 2025
- Start date
- 27 Dec 2023
- Primary completion date
- 31 Dec 2025
- Lead sponsor
- National Cancer Center, Korea
- Diseases
- Childhood cancers
- NCT number
- NCT06969742
What you commit to
- Study type: Interventional
- Planned participants: 120
- From 27 Dec 2023 to the primary completion date, 31 Dec 2025
- 3 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Those undergoing treatment and children and adolescent survivors of acute-transitional phase, whose prior intelligence assessment FSIQ score is less than 70. However, if the GAI score is 70 or higher, participation is possible after the principal investigator's interview, with linguistic competence taken into consideration.
- Elimination Criteria:
Other illness
- Those whose psycho-emotional state requires professional treatment or medical conditions precludes intervention.
- Those who have difficulty participating due to worsening of disease or decease of patient.
Other
- Those who disagree to participate as a research subject.
- Those who withdraw consent of this research.
Who the study is looking for
- Those between the ages of 10 and 24, and diagnosed with pediatric solid tumor, who are undergoing treatment or survivors who have completed the treatment and the treatment end date is within 2 years.
- Parent or legal guardian who is a primary caregiver to children and adolescent patient of acute-transitional phase.
- Those whose cognitive ability is capable of verbal counseling and who agrees to the evaluation assessment.
Age in the registry: 10 years to 24 years · Sex: All · Does not accept healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| National Cancer Center Coordinator of this site? Confirm its status | Goyang-si | South Korea | Recruiting |
| Tree and Forest Psychological Counseling Center Coordinator of this site? Confirm its status | Seoul | South Korea | Active, not recruiting |
| Seoul National University Children's Hospital Coordinator of this site? Confirm its status | Seoul | South Korea | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.