A Stress Management and Resiliency Program for Adolescent and Young Adult Survivors (NCT03768336) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
A Stress Management and Resiliency Program for Adolescent and Young Adult Survivors
United States72 participantsStarted 2019-04-01
Plain-language summary
This research study aims to explore the feasibility and acceptability of an adapted resiliency group program, called the Relaxation Response Resiliency Program (3RP-AYA), to reduce stress and promote stress-management among adolescents and young adults who have completed treatment for cancer.
Who can participate
Age range
16 Years – 29 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Diagnosed with any cancer between ages 14 and 29
* Completed cancer treatment within the past 5 years
* At least 16 years of age at time of enrollment
Exclusion Criteria:
* Unwilling or unable to participate in the study
* Unable to speak or read English
* Is medically or otherwise unable to participate (as determined by a physician or study PI)
* Unwilling or unable to participate in study sessions delivered via the Partners Telehealth videoconferencing software
* Participation in a focus group during Phase 1 (DF/HCC 17-315)
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
3RP-AYA Feasibility: Percent of Identified Eligibles Who Enroll
Timeframe: Post-treatment completion (treatment is approximately 8 weeks)
2
3RP-AYA Feasibility: Proportion of Participants Completing the 3RP-AYA Program
Timeframe: Post-treatment completion (treatment is approximately 8 weeks)
3
3RP-AYA Acceptability: Five Questions
Timeframe: Post-treatment completion (treatment is approximately 8 weeks)