Understanding patient and caregiver experiences in neuro-oncology care
Patient and Caregiver Priorities in Neuro-Oncology Care
Mayo Clinic · NCT06676306
This study looks at the challenges faced by patients with brain tumors and their caregivers to better understand their experiences during diagnosis and treatment.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 80 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Mayo Clinic (other) |
| Locations | 1 site (Rochester, Minnesota) |
| Trial ID | NCT06676306 on ClinicalTrials.gov |
What this trial studies
This observational study aims to identify the burdens faced by patients and caregivers in the diagnosis and treatment of central nervous system tumors. It focuses on characterizing the symptom burden experienced by patients and the needs of caregivers. Participants will engage in semi-structured interviews, and their medical records will be reviewed to gather comprehensive insights. The study seeks to highlight important treatment outcomes from the perspectives of both patients and caregivers.
Who should consider this trial
Good fit: Ideal candidates include adults aged 18 and older diagnosed with primary or metastatic CNS tumors who are willing to participate in interviews.
Not a fit: Patients with uncontrolled illnesses or those unable to participate in interviews may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance support systems for patients and caregivers dealing with CNS tumors.
How similar studies have performed: Other studies have successfully explored patient and caregiver experiences in oncology, indicating that this approach is valuable and relevant.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria:
* \* Age ≥ 18 years.
* Diagnosis of primary or metastatic CNS tumor with a primary caregiver, should patient wish to involve one.
* Willing and able to participate in a semi-structured interview lasting approximately 60 minutes. Dyad interviews conducted for participants who elect to involve a caregiver.
* Willing and able to participate in a single follow-up interview. Dyad follow up interviews conducted for participants who elect to involve a caregiver.
Exclusion Criteria:
* \* Uncontrolled and/or intercurrent illness which limits participation in study interview.
* Vulnerable populations: pregnant or nursing persons, prisoners, or persons lacking capacity for understanding.
* Unable to read and speak English.
* Note: English does not need to be primary language.
Where this trial is running
Rochester, Minnesota
- Mayo Clinic in Rochester — Rochester, Minnesota, United States (RECRUITING)
Study contacts
- Principal investigator: Ugur T. Sener, MD — Mayo Clinic in Rochester
- Study coordinator: Clinical Trials Referral Office
- Email: mayocliniccancerstudies@mayo.edu
- Phone: 855-776-0015
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Malignant Central Nervous System Neoplasm, Metastatic Malignant Neoplasm in the Central Nervous System