Virtual Group Resilient Living for Advanced Cancer
Official title: Virtual Group Resilient Living Program For Patients Living With Advanced Cancer
Run by Mayo Clinic · NCT07659158 · Data updated 2026-11-12
A group-based online program tests whether seven weekly sessions can reduce anxiety and fatigue and improve quality of life for adults with advanced cancer.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 42 (estimated) |
| Sponsor | Mayo Clinic Academic / other |
| Locations | 1 site (Rochester, Minnesota) |
| Status | Recruiting |
| Started | June 19, 2026 |
| Main results expected | June 30, 2027 |
| Study ends | June 30, 2027 |
| Registry record updated | July 2, 2026 |
| Trial ID | NCT07659158 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with advanced (stage III/IV) cancer, English-speaking, with baseline distress, internet access, and the ability to participate in seven online group sessions and complete surveys.
✕Probably not a fit
Patients without significant distress or those unable to engage in online sessions may see little or no personal benefit from the program.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a prospective, single-arm study conducted virtually at Mayo Clinic to test the feasibility and potential benefits of a 7-week Virtual Group Resilient Living Program. Participants learn stress-management and resilience techniques such as mindfulness, positive reframing, gratitude, compassion, acceptance, meaning, and forgiveness in a group setting, with the aim of improving anxiety, stress, quality of life, coping, and fatigue. The study also collects survey data to assess feasibility and preliminary effectiveness, and is designed for minimal risk. Eligibility requires adults with stage III/IV cancer, baseline distress, English fluency, internet access, and ability to participate in online sessions.
Why it matters
Potential benefit: If successful, participants may experience reduced anxiety and fatigue and improved quality of life through enhanced coping and resilience.
How similar studies have gone: Prior psychosocial programs with online group formats have shown feasibility and potential benefits in cancer populations, but this specific seven-session virtual resilience program is being explored for feasibility and signals of effectiveness.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * English fluency * Diagnosis of advanced (stage III/IV) malignancy * Baseline distress score ≥ 4/10. Patients can answer questions orally rather than complete worksheet, if applicable * Life expectancy of ≥ 6 months * Provide informed consent * Ability to complete questionnaire(s) by themselves or with assistance * Has a reliable internet connection * Has the ability to utilize technology to watch online modules, \& participate in virtual sessions Exclusion Criteria: * As determined through self-report, those diagnosed with a history of a psychotic episode ≤ 5 years * All psychological co-morbidities such as a history of untreated schizophrenia, \& bipolar disease * A diagnosis of severe cognitive impairment
Where it's running
-
Mayo Clinic in Rochester
Rochester, Minnesota, United States Recruiting
Study contacts
- Principal investigator: Deirdre R. Pachman, MD — Mayo Clinic
- Study coordinator: Clinical Trials Referral Office
- Email: mayocliniccancerstudies@mayo.edu
- Phone: 855-776-0015
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.