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Behavioral Intervention

Virtual Group-Based Physical Activity for Cancer Survivors

N/A
Waitlist Available
Led By Celina H Shirazipour, Ph.D.
Research Sponsored by Cedars-Sinai Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks
Awards & highlights
No Placebo-Only Group

Summary

This trial will test whether group-based physical activity, delivered virtually, is feasible for AYA cancer survivors who have completed treatment. 20 participants will be enrolled for 3 months.

Who is the study for?
This trial is for young adult cancer survivors aged 18-39 who have finished treatment at least 3 months ago, are not currently very active, and can use internet-connected devices. It's not for those with severe hearing or vision loss, pregnant individuals, or anyone planning to undergo major cancer treatments within the next three months.
What is being tested?
The study tests a virtual group exercise program called BurnAlong and a social media discussion board to see if they're doable for these survivors. All participants will try out the online fitness classes and join discussions over about three months.
What are the potential side effects?
Since this trial involves physical activity and social media use rather than medication, typical drug side effects aren't expected. However, participants may experience general exercise-related discomforts like muscle soreness.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Feasibility of BurnAlong
Secondary study objectives
Adolescent and Young Adult Psycho-Oncology Screening Tool (AYA-POST)
Health Action Process Approach Inventory (HAPA Inventory)
Measure of Experiential Aspects of Participation (MeEAP)
+6 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Virtual Group-Based Physical Activity (BurnAlong) and Discussion BoardExperimental Treatment1 Intervention
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.

Find a Location

Who is running the clinical trial?

Walter Reed National Military Medical CenterFED
140 Previous Clinical Trials
33,165 Total Patients Enrolled
Cedars-Sinai Medical CenterLead Sponsor
512 Previous Clinical Trials
163,356 Total Patients Enrolled
3 Trials studying Lymphoma
54 Patients Enrolled for Lymphoma
Celina H Shirazipour, Ph.D.Principal InvestigatorCedars-Sinai Medical Center
1 Previous Clinical Trials
80 Total Patients Enrolled
~2 spots leftby Nov 2025