Quality of Life Intervention for Patients Receiving Radiation Therapy for Advanced Cancer Treatment and Their Caregivers
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Cancer, Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 2/8/2019 |
| Start Date: | July 2016 |
| End Date: | June 2019 |
A Structured Multidisciplinary Quality of Life Intervention for Patients Receiving Radiation Therapy for Advanced Cancer Treatment & Their Caregivers: A Telemedicine Project
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.
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.
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.
We found this trial at
3
sites
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials