Clinical trial · Interventional
POZIKIDS: Exercise and Comprehensive Care to Improve the Quality of Life of Children and Adolescents With Cancer
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Objective: To assess the feasibility of a supervised, controlled and personalised physical exercise programme and its potential efficacy in improving functional capacity and quality of life in children and adolescents with cancer. Design: Hybrid quasi-experimental pilot trial, clinical and phase I implementation. Methods: The learning collaborative approach based on the Institute for Healthcare Improvement Breakthrough Series Collaborative Model will be followed through quarterly Plan-Do-Study-Act (P-D-S-A) cycles. Participants: For feasibility, at least, 45 patients will be included in 3 successive PDSA cycles of at least 15 patients each, aged 4-18 years diagnosed with any type of cancer. Variables: clinical and socio-demographic, body composition, physical condition and mobility, quality of life, physical activity and implementation. Intervention: Everyone will receive a physical exercise intervention combining strength and aerobic capacity work. Initially it will be carried out in the hospital setting, and later in streaming supervised by a professional. The intervention will be modelled through a formative evaluation process with the collaboration of all the agents involved, experimenting in each cycle with an increasingly adapted version of the exercise programme. Statistical analysis: Recruitment rates will be calculated, characteristics associated with project participation and adherence to the exercise programme will be identified. Outcome variables will be compared before and after the intervention, identifying those with the greatest validity, reliability and sensitivity to change, which will then be used in phase II and III trials.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Childhood Cancer | Childhood Malignant Neoplasm | ALIAS | 0.90 |
| Exercise | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Physical exercise program | Other | — | UNRESOLVED |
| Type of the physical exercise program | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (11)
- measure
- Quarterly recruitment rates assessed by comparing those who participate with those who do not.
- timeFrame
- 2 years
- description
- To assess the feasibility of the exercise programme, quarterly recruitment rates will be calculated over the recruitment and follow-up period, and socio-demographic and morbidity variables associated with study participation will be identified, comparing those who participate with those who do not, using logistic regression analysis.
- measure
- Adherence rates assessed by the proportion of sessions completed and adherence to the prescribed exercise protocol
- timeFrame
- 2 years
- description
- Participants' adherence to the programme will be described in terms of the proportion of sessions completed and compliance with the exercise protocol prescribed for each patient, and variables associated with compliance will be identified.
- measure
- Body composition assessed by the Body Mass Index
- timeFrame
- 2 years
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 4 Years
- Maximum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patients diagnosed with cancer and other neoplasms * Age between 4 and 18 years at the time of inclusion in the study * Patients diagnosed with cancer and other malignancies aged between 4 and 18 years who are experiencing relapse * Paediatric patients requiring chemotherapy, radiotherapy, or oncological surgery * Patients and parents or guardians who agree to participate in the study and sign the informed consent forms by current legislation depending on the patient's age. Exclusion Criteria: * Patients with cognitive deficits that prevent participation in and performance of physical exercise interventions. * Patients with severe neurological pathology with a motor impairment that prevents or significantly hinders the performance of physical exercise * Patients and families or guardians with language comprehension difficulties that make it difficult or impossible to carry out the physical exercise intervention. * Patients \< 16 years with a functional status score according to Lanskyi scale \<60% * Patients \> 16 years with Karnofsky scale \<60%. * Any other criteria that the physician deems inappropriate for participation in the study
References
Publications (0)
Data not yet available