NCT07228533Not yet recruiting
CesiKids Trial: Enhancing Psychological Resilience in Adolescents With Cancer
Evaluation of the Effectiveness of a Nursing-Based Co-Design Intervention Program (CesiKids) to Enhance Psychological Resilience in Hospitalized Adolescents Diagnosed With Cancer: A Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 14 Nov 2025
Brief summary (registry, in English)
This study will develop and evaluate a mobile-based co-design intervention (CesiKids) to enhance psychosocial resilience in hospitalized adolescents aged 12-18 diagnosed with cancer. The program will be created using Bronfenbrenner's Ecological Systems Theory and designed in collaboration with nurses, recovered adolescents, and parents. A randomized controlled design will be used. The intervention group will participate in a four-week structured program, while the control group will receive standard care. Psychosocial resilience and coping outcomes will be assessed at baseline, post-intervention, and follow-up. This research aims to offer an evidence-based, scalable model to support resilience among adolescents with cancer in clinical settings.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 36 (estimated)
- First submitted
- 13 Nov 2025
- Start date
- 1 Nov 2025
- Primary completion date
- 31 Jan 2027
- Lead sponsor
- Eskisehir Osmangazi University
- Diseases
- Childhood cancers
- NCT number
- NCT07228533
What you commit to
- Study type: Interventional
- Planned participants: 36
- From 1 Nov 2025 to the primary completion date, 31 Jan 2027
- 1 site 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
- Receiving hematopoietic stem cell transplantation treatment,
Other illness
- Experiencing communication difficulties (e.g., intellectual disability, visual impairment, etc.),
- Having a psychiatric diagnosis made by a psychiatrist,
Other
- Having developed a relapse after remission,
- Having experienced a significant life event affecting psychological well-being within the past four weeks (e.g., death, divorce, etc.).
Who the study is looking for
- Parents have provided informed consent after receiving information,
- The child has given assent to participate after being informed,
- The child is between 12 and 18 years of age,
- The child has been diagnosed with cancer and is currently receiving inpatient treatment,
- The child is undergoing chemotherapy and/or radiotherapy,
- The child is able to use a computer and/or smartphone,
- The child can understand and speak Turkish.
Age in the registry: 12 years to 18 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Ankara University Faculty of Medicine Cebeci Research and Practice Hospital Coordinator of this site? Confirm its status | Ankara | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.