The BurnAlong Pilot Study for Adolescent and Young Adult Cancer Survivors

  • STATUS
    Recruiting
  • End date
    Jan 9, 2024
  • participants needed
    20
  • sponsor
    Cedars-Sinai Medical Center
Updated on 12 March 2022
cancer
cancer treatment
primary cancer
Accepts healthy volunteers

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.

Description

This is a single-arm, prospective, interventional pilot study.

Adolescent and young adult (AYA) survivors of cancer (n=20) will engage in three months of virtually group physical activity (PA) delivered via BurnAlong, a wellness platform and online app.

Participants will be asked to engage in a BurnAlong workout session with a partner (friend/spouse/child/fellow study participant) a minimum of three times a week for 3 months.

Participants will also meet monthly with an exercise physiologist for a customized exercise session. Participants are allowed to engage in additional PA and non-PA sessions on BurnAlong as desired.

Participants will also be asked to engage in a private social network discussions around key topics of interest for AYA communities with a focus on post-traumatic growth and positive psychology with a minimum of 2 post engagements a week for 3 months.

Participants will complete surveys and physical assessments at baseline and at end of study.

Participants also participate in a 1 hr qualitative exit interview about their well-being, participation experiences, and experience with using the BurnAlong platform.

Details
Condition Cancer, Cancer Metastatic, Neoplasms, Breast Cancer, Lung Cancer, Thyroid Cancer, Lymphoma, Lymphoma, Non-Hodgkin, Hodgkin Lymphoma, Leukemia, Sarcoma, Skin Cancer, Bone Cancer, Gynecologic Cancer, Pancreas Cancer, Multiple Myeloma, Colorectal Cancer, Gastrointestinal Cancer, Prostate Cancer, Glioblastoma, Brain Cancer, Head and Neck Cancer
Treatment Virtual group based physical activity (BurnAlong) and Social Media Discussion Board
Clinical Study IdentifierNCT05131815
SponsorCedars-Sinai Medical Center
Last Modified on12 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Cancer (all types) diagnosis between the ages of 15-25
Between the ages of 18-25 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

Exclusion Criteria

Hearing loss or vision impairment that would preclude the participant from accessing and using the app (use of hearing aids or visual aids is acceptable) based on self-report
Currently meeting physical activity guidelines (score of >23 on Godin-Shephard Leisure-Time Physical Activity Questionnaire)
Currently pregnant, based on self-report
Patients with active treatment planned within the next 3 months. (Active treatment includes chemotherapy, biologic therapy, radiation therapy, surgery, and any combination.) Long-term hormonal/biologic treatments are acceptable except for AR-targeted therapies for prostate cancer. Participants with known metastatic disease, grade 3 or higher neuropathy, major surgery within 3 months of baseline visit, pregnancy of childbearing potential will be excluded
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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