Neoplasms Clinical Trial
— PEACEOfficial title:
Pediatric Early Rehabilitation in ACute Lymphoblastic LEukemia (PEACE): A Feasibility Study of a Hybrid Delivery Format
The purpose of this study is to determine the feasibility and acceptability of a hybrid in-person and virtual individualized physiotherapy program using the Healthy Eating and Active Living (HEAL-ME) online platform for children diagnosed with acute lymphoblastic leukemia. We would like to know if this type of hybrid program delivery model is feasible, and if children and their parents are willing and able to participate in the program. We will do this by recording how many, and what type of physiotherapy sessions (in-person or virtual) are completed, what resources offered on the platform are accessed, and how many children complete the assessments.
Status | Recruiting |
Enrollment | 10 |
Est. completion date | December 31, 2024 |
Est. primary completion date | December 31, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 4 Years to 17 Years |
Eligibility | Inclusion Criteria: 1. Children diagnosed with acute lymphoblastic leukemia aged between 4 and 17 years (at time of diagnosis) and their mother, father, or primary carer; 2. Undergoing or completed cancer treatment as established by the Children's Oncology Group; 3. Access to the internet through a home computer or tablet; 4. Patient or caregiver is able to speak and comprehend English; and 5. The child is approved by their Oncologist to participate in the program. Exclusion Criteria: 1. Children with a history of a neurodevelopmental or genetic disorder (i.e., Down syndrome, autism, seizure disorder) prior to the cancer diagnosis; and 2. Children with a concurrent condition (illness, disease, psychiatric disorder), as determined by oncologist or physiotherapist, that would compromise study participation or interpretation of study results. |
Country | Name | City | State |
---|---|---|---|
Canada | University of Alberta | Edmonton | Alberta |
Lead Sponsor | Collaborator |
---|---|
University of Alberta | Alberta Health services |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Retention rate | The number of participants completing the intervention and assessments | Post-intervention: 12 weeks | |
Secondary | Recruitment rate | Number eligible divided by the number of participants enrolling in the study | One year | |
Secondary | Adherence to study intervention | Attendance rates for in-person and virtual physical therapy sessions | Post-intervention: 12 weeks | |
Secondary | Adverse events | Number of serious and non-serious adverse events | One year | |
Secondary | Acceptability | Satisfaction survey | Post-intervention: 12 weeks | |
Secondary | Health-related Quality of Life | Pediatric Quality of Life Inventory Version 4: Total scale score, with higher scores reflecting better quality of life | Post-intervention: 12 weeks |
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