The BurnAlong Pilot Study: Examining the Feasibility of a Virtual Group-based Physical Activity Intervention for Adolescent and Young Adult Cancer Survivors

Status: Completed
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this prospective, interventional, single-arm pilot study is to evaluate whether virtually delivered group-based physical activity is feasible for adolescent and young adult (AYA) cancer survivors. AYAs who were diagnosed with cancer and have completed cancer treatment will be recruited for this study. This study will enroll 20 participants in total and will last approximately 3 months.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 39
Healthy Volunteers: t
View:

• Cancer (all types) diagnosis between the ages of 15-39

• Between the ages of 18-39 during study participation

• At least 3 months post-active treatment completion

• Answers no to all questions on the Physical Activity Readiness Questionnaire

• Not currently meeting physical activity guidelines per leisure-time physical activity participation questionnaire

• Access to and ability to use a computer, tablet or phone device with internet access

• Ability to understand and read English

• Written informed consent obtained from subject and ability for subject to comply with the requirements of the study

Locations
United States
California
Cedars-Sinai Medical Center
Los Angeles
Time Frame
Start Date: 2022-07-25
Completion Date: 2023-06-15
Participants
Target number of participants: 8
Treatments
Experimental: Virtual Group-Based Physical Activity (BurnAlong) and Discussion Board
Participants will be asked to complete a 12 week virtual physical activity program delivered by the BurnAlong app, participate in a discussion board, and engage in live physical activity sessions with an exercise physiologist.
Authors
Laurel Finster
Sponsors
Collaborators: Walter Reed National Military Medical Center
Leads: Cedars-Sinai Medical Center

This content was sourced from clinicaltrials.gov

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