Viewing Study NCT06012825



Ignite Creation Date: 2024-05-06 @ 7:26 PM
Last Modification Date: 2024-10-26 @ 3:07 PM
Study NCT ID: NCT06012825
Status: COMPLETED
Last Update Posted: 2023-11-21
First Post: 2023-05-04

Brief Title: Pediatric Physical Activity for Children With Cancer
Sponsor: University of Hawaii
Organization: University of Hawaii

Study Overview

Official Title: Pediatric Physical Activity PePA Understanding Best Practices in Implementing Physical Activity for Patients Diagnosed With Childhood Cancer
Status: COMPLETED
Status Verified Date: 2023-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: PePA
Brief Summary: The goal of this pilot study is to test the feasibility and participant adherence pediatric patients diagnosed with childhood cancer to a virtual 12-week physical activity program

The aims of this project are to

1 Determine the feasibility of administering the program and patient acceptability
2 Report program adherence and completion rates
3 Explore trends on the impact of a virtual PA intervention on psychosocial health and physical fitness

Participants will undergo pre- and post-assessments including measurements of fitness self-reported fatigue and depression symptoms social support and current amount of physical activity Patients will then be invited to participate in two consecutive 12-week virtual physical activity interventions with similar-aged peers 2xweek 60 minutessession over 2 rounds
Detailed Description: It is critical for childhood cancer patients to maintain a physical activity PA regime as they are at an increased risk of developing co-morbidities PA engagement is associated with positive psychosocial outcomes and it has the potential to improve cardiopulmonary and musculoskeletal function Patients will be enrolled and will undergo baseline assessments of fitness and quality of life as part of their standard care and additional measures that include fatigue depression social support and PA volume will be measured Patients will be invited to participate in a 12-week virtual PA intervention with similar-aged peers 2xweek 60 minutessession Patients will be led through activities that are culturally relevant and age-appropriate At the end of the 12-week intervention the same tests will be completed The patients will have an opportunity to receive 2 interventions A mixed method design will be used where quantitative data will include information related to feasibility PA volume physical fitness and psychosocial health measures and qualitative data will be collected from the patients during the focus groups

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None