A Resilience-Based Approach to Improve Long-term Quality of Life in Post-treatment Lymphoma Survi… (NCT07013435) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
A Resilience-Based Approach to Improve Long-term Quality of Life in Post-treatment Lymphoma Survivorship
United States254 participantsStarted 2026-08-31
Plain-language summary
The goal of this trial is to learn if a resilience intervention can lead to improvements in lymphoma survivors' quality of life.
Who can participate
Age range
18 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:
* English or Spanish speaking adults (18+ at time of enrollment)
* Within 2 years of completing active, curative treatment for lymphoma (includes surgery, chemotherapy, immunotherapy, radiation therapy, or other)
Exclusion Criteria:
* Active psychiatric or cognitive comorbidity as determined by the site PI or treating clinician
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.
1This trial is focused on resilience and quality of life after lymphoma treatment rather than treating the cancer itself — is this something worth considering once my active treatment is complete, or would it overlap with where I am right now in my care?
2The study is measuring quality of life using something called the PROMIS-29 — can you explain what that tool tracks, and whether the kinds of changes it measures would be meaningful improvements in my day-to-day life as a lymphoma survivor?
3Since this trial is listed as 'not yet recruiting,' do you know when it might open to patients, and is there anything I should be doing in the meantime to prepare or to stay on your radar as a potential candidate to discuss later?
4This trial is listed as Phase NA, which I understand often applies to behavioral or supportive care studies rather than drug trials — does that mean the risk profile is different from a typical drug trial, and what should I know about what participating would actually involve?
5Are there existing resilience-based programs or survivorship support services I could access now, and how would those compare to what this trial might offer once it opens?
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.