Pilot Program to Personalize Care & Improve Quality of Life for Women With Ovarian Cancer
| Status: | Completed |
|---|---|
| Conditions: | Ovarian Cancer, Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/21/2016 |
| Start Date: | January 2010 |
| End Date: | September 2015 |
A Pilot Program to Personalize Care by Integrating Traditional and Complementary Medicine for Women With Ovarian Cancer
The purpose of this study is to find out if complementary and alternative medicines (CAM)
should be included with traditional therapy for women with ovarian cancer. Some of the
alternative medicines include non-traditional drug and herbal therapies along with dietary
and nutritional strategies. Only a few of these alternative medicines have been tested with
women with ovarian cancer.
should be included with traditional therapy for women with ovarian cancer. Some of the
alternative medicines include non-traditional drug and herbal therapies along with dietary
and nutritional strategies. Only a few of these alternative medicines have been tested with
women with ovarian cancer.
The study will be offered to women with ovarian cancer who are receiving care at the
Gynecologic Oncology Clinic at H. Lee Moffitt Cancer Center. Prospective candidates,
identified via chart review, will receive a mailing that describes and invites them to be
screened for eligibility. Potential participants seen in the clinic will also be approached
and invited to participate.
The informed consent process and pretesting will take place in the clinic, with exceptions
made as needed for women who prefer to complete documents at home.
The intervention, which will consist of four educational CAM sessions, will be held on site
in a private room at Moffitt Cancer Center. Immediately before and after each session, we
will administer a brief on-site pre- and post-test. Upon completion of the intervention,
participants will be asked to complete a post-test on site or at home, depending on their
preference. Follow-up telephone calls will be made to the participants at 8 weeks after the
last session.
Pre- and post-test measures will focus on quality of life, prior use of CAM therapies, topic
preferences, knowledge gained from the presentations, changed intentions and behaviors
associated with CAM, and satisfaction with the program.
Gynecologic Oncology Clinic at H. Lee Moffitt Cancer Center. Prospective candidates,
identified via chart review, will receive a mailing that describes and invites them to be
screened for eligibility. Potential participants seen in the clinic will also be approached
and invited to participate.
The informed consent process and pretesting will take place in the clinic, with exceptions
made as needed for women who prefer to complete documents at home.
The intervention, which will consist of four educational CAM sessions, will be held on site
in a private room at Moffitt Cancer Center. Immediately before and after each session, we
will administer a brief on-site pre- and post-test. Upon completion of the intervention,
participants will be asked to complete a post-test on site or at home, depending on their
preference. Follow-up telephone calls will be made to the participants at 8 weeks after the
last session.
Pre- and post-test measures will focus on quality of life, prior use of CAM therapies, topic
preferences, knowledge gained from the presentations, changed intentions and behaviors
associated with CAM, and satisfaction with the program.
Inclusion Criteria:
- A diagnosis of ovarian cancer
- An Eastern Cooperative Oncology Group (ECOG) score of 2 or less with a life
expectancy of at least 12 months
- A patient being treated by a gynecologic oncologist in the Center for Women's
Oncology
- Ability to read, understand, and sign the informed consent form
- Ability to read, write and understand English, which will be the language used in the
materials and oral presentations
- Willingness to complete pre-test and post-test questionnaires
- Willingness to complete brief questionnaires at each session
- Willingness to participate in one follow-up telephone interview at 8 weeks after the
final session
- Willingness to participate in four sessions that take place at Moffitt Cancer Center
- Access to transportation, with the ability to travel to and from Moffitt to
participate in the sessions
We found this trial at
1
site
12902 USF Magnolia Dr
Tampa, Florida 33612
Tampa, Florida 33612
(888) 663-3488
H. Lee Moffitt Cancer Center & Research Institute Moffitt Cancer Center in Tampa, Florida, has...
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