Quality of Life Intervention for Patients Receiving Radiation Therapy for Advanced Cancer Treatment and Their Caregivers

Overview

About this study

This study will use video technology in conjunction with in-person participation. This is a pilot project, where all enrolled participants will receive the multidisciplinary intervention. Participants (patients and caregivers) from Mayo Clinic Rochester will attend an in-person group session, and participants (patients and caregivers) from Mayo Clinic Florida or Northfield Mayo Clinic Radiation Oncology Center will participate through the use of video conferencing. The goals are to examine feasibility (percent of eligible patients and caregivers who enroll), attrition, and adherence (attend at least four of the six sessions), to determine any differences between the two formats, and to examine potential QOL differences as a result of the intervention.

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:

18 years of age.
Ability to attend all treatment sessions and follow-up.
Ability to provide written informed consent.
Ability to participate in all aspects of the study.
Initial diagnosis of cancer must have been 12 months prior to study entry.
Intermediate to poor prognosis, defined as an expected 5-year survival of 0%-50% in the judgment of the physicians entering the patient on the study.
Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0, 1, or 2.
1 week of planned cancer treatment (radiation or chemotherapy) at Mayo Clinic.
Has a caregiver also willing to participate.
Willingness to get e-mail/text reminder to complete the follow-up survey or complete the follow-up survey with a study coordinator by phone.

Exclusion Criteria:

Expected survival of <6 months.
Active substance abuse (alcohol or drug).
Participation in other psycho-social research trials.
Active untreated thought disorder (bipolar illness, schizophrenia, etc.).
Untreated suicidal intent or plan.
In need of psychiatric hospitalization.
Recurrent disease after disease-free interval of >6 months.
Previous cancer 5 years (except non-melanoma skin cancer and/or second cancer diagnosed at approximately the same time as this cancer).
Use of Proton Beam Radiation.

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
Rochester, Minn. Mayo Clinic principal investigator Matthew Clark, Ph.D., L.P.	Closed for enrollment
Jacksonville, Fla. Mayo Clinic principal investigator Teresa Rummans, M.D.	Closed for enrollment

Mayo Clinic Location

Status

Rochester, Minn.

Mayo Clinic principal investigator

Matthew Clark, Ph.D., L.P.

Closed for enrollment

Jacksonville, Fla.

Mayo Clinic principal investigator

Teresa Rummans, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Clinical Trials