Phase I/II Cancer Caregiver Interventions to Improve Quality of Life and Prevent Burnout
Overview
Tab Title Description
Study type
InterventionalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Jacksonville, Florida: 13-002943
- Rochester, Minnesota: 13-002943
NCT ID: NCT02166866
Sponsor Protocol Number: MC1295
About this study
This study defines cancer caregivers as unpaid individuals who provide physical, practical, and/or emotional care and support to the cancer patient in the home setting. They may participate in this study if care recipients and the caregiver are both adults (18 years or older), with the patient having been diagnosed with cancer.The 8 intervention sessions will target the five domains of Quality Of Life (emotional, physical, social, cognitive, and spiritual well-being), be provided in group settings, and be delivered in two 45-minute sessions each week over a 4-week period.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:
- Ability to provide written informed consent.
- Ability to speak, read, write and understand English language
- Has cancer caregiver status defined as an unpaid individual who provides physical, practical, and/or emotional care and support to a cancer care recipient in the home or other healthcare setting.
- Has a care recipient:
- ≥ 18 years of age who
- has a malignancy (either solid tumor or hematologic) diagnosis.
- who has signed a research authorization form
- who is undergoing or in the last 6 months has undergone cancer treatment
- Ability to use and access to a computer, tablet or other device with internet access and video capabilities
Exclusion Criteria:
- Diagnosis within the past 12 months of active substance abuse (alcohol or drugs)
- Diagnosis within the past 12 months of active mental health condition that has required psychiatric hospitalization
- Diagnosis within the past 12 months of suicidal thoughts or attempt
- Care recipient is currently participating in another psychosocial clinical trial
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
| Mayo Clinic Location |
Status |
Contact |
Jacksonville, Fla.
Mayo Clinic principal investigator Maria Lapid, M.D. |
Closed for enrollment |
Contact information:
Cancer Center Clinical Trials Referral Office
855-776-0015
|
Rochester, Minn.
Mayo Clinic principal investigator Maria Lapid, M.D. |
Closed for enrollment |
Contact information:
Cancer Center Clinical Trials Referral Office
855-776-0015
|
More information
Publications
Publications are currently not available