Efficacy of Cancer Support Programs: A Social Comparison Theory Analysis
Status: | Active, not recruiting |
---|---|
Conditions: | Prostate Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 21 - Any |
Updated: | 4/17/2018 |
Start Date: | May 2009 |
End Date: | May 2020 |
The goal of this research study is to learn if a support group program is acceptable for
patients with prostate cancer or patients with breast cancer. Researchers also want to learn
if the characteristics of the members of the support group program can have an effect on the
quality of life of other members of the support group program. Support group programs will be
conducted separately for prostate cancer patients and breast cancer patients.
patients with prostate cancer or patients with breast cancer. Researchers also want to learn
if the characteristics of the members of the support group program can have an effect on the
quality of life of other members of the support group program. Support group programs will be
conducted separately for prostate cancer patients and breast cancer patients.
Screening Questionnaires:
Signing this consent form does not mean that you will be able to take part in this study. You
will complete some questions about your mood to help researchers decide if you are eligible
to take part in this study. It will take 10 to 15 minutes to complete these questions.
The researcher will discuss the questionnaire results with you and provide you with a list of
community referrals and resources.
If your responses to the questions show that you are distressed, you will be eligible to take
part in this study. If your responses to the questions show that you are not distressed, you
will be randomly selected (as in the flip of a coin) to take part in this study.
If your responses to the questions show that you may harm yourself, a licensed psychologist
will follow-up with you and make recommendations for future treatment.
Study Questionnaires:
If you are found to be eligible and are selected to take part in this study, you will be
asked to complete questionnaires that will have questions about your medical history, quality
of life, mood, thought processes, methods of coping with the disease, and support that you
receive from others. It will take about 1 hour to complete these questionnaires.
Support Groups:
You will also take part in a support group program for either prostate or breast cancer
patients. Each support group will be made up of about 10 members. Each group will meet 1 time
each week for 10 weeks. Each meeting will last about 2 hours. At each meeting, patients will
discuss and learn about methods of coping with the disease and ways to relax.
All meetings will be audio-recorded. Recordings will be reviewed by the research team to make
sure that the groups are covering the program content.
Length of Study:
You will be on study for about 3 months.
End-of Study Questionnaires:
After the last support group meeting, you will complete questionnaires that will ask
questions about your medical history, quality of life, mood, thought processes, methods of
coping with the disease, and support that you receive from others. You will be off study
after you have completed the end-of-study questionnaires.
This is an investigational study.
Up to 240 patients will take part in this study. Up to 204 will be enrolled at MD Anderson.
Signing this consent form does not mean that you will be able to take part in this study. You
will complete some questions about your mood to help researchers decide if you are eligible
to take part in this study. It will take 10 to 15 minutes to complete these questions.
The researcher will discuss the questionnaire results with you and provide you with a list of
community referrals and resources.
If your responses to the questions show that you are distressed, you will be eligible to take
part in this study. If your responses to the questions show that you are not distressed, you
will be randomly selected (as in the flip of a coin) to take part in this study.
If your responses to the questions show that you may harm yourself, a licensed psychologist
will follow-up with you and make recommendations for future treatment.
Study Questionnaires:
If you are found to be eligible and are selected to take part in this study, you will be
asked to complete questionnaires that will have questions about your medical history, quality
of life, mood, thought processes, methods of coping with the disease, and support that you
receive from others. It will take about 1 hour to complete these questionnaires.
Support Groups:
You will also take part in a support group program for either prostate or breast cancer
patients. Each support group will be made up of about 10 members. Each group will meet 1 time
each week for 10 weeks. Each meeting will last about 2 hours. At each meeting, patients will
discuss and learn about methods of coping with the disease and ways to relax.
All meetings will be audio-recorded. Recordings will be reviewed by the research team to make
sure that the groups are covering the program content.
Length of Study:
You will be on study for about 3 months.
End-of Study Questionnaires:
After the last support group meeting, you will complete questionnaires that will ask
questions about your medical history, quality of life, mood, thought processes, methods of
coping with the disease, and support that you receive from others. You will be off study
after you have completed the end-of-study questionnaires.
This is an investigational study.
Up to 240 patients will take part in this study. Up to 204 will be enrolled at MD Anderson.
Inclusion Criteria:
1. Diagnosis of prostate or breast cancer, regardless of treatment
2. No evidence of metastatic disease
3. Able to read, speak, and write English
4. Resides within one hour of M.D. Anderson Cancer Center
5. 21 years of age or older
6. Able to provide meaningful informed consent as judged by a research team member
7. Being a distressed patient: a T score greater than or equal to 63 on the Global
Severity Index (GSI) of the Brief Symptom Inventory (BSI) or a T score greater than or
equal to 63 on any two primary dimensions of this measure, or being a non-distressed
patient: a T score of < 63 on the GSI and a T score of <63 on all primary dimensions
of the BSI.
Exclusion Criteria:
1) None
We found this trial at
1
site
1515 Holcombe Blvd
Houston, Texas 77030
Houston, Texas 77030
713-792-2121
University of Texas M.D. Anderson Cancer Center The mission of The University of Texas MD...
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