Stress Reduction in Improving Quality of Life in Patients With Recurrent Gynecologic or Breast Cancer
NCT01764789 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 39
Last updated 2015-10-09
Summary
This pilot clinical trial studies stress reduction in improving quality of life in patients with recurrent gynecologic or breast cancer. Participating in a stress reduction program may help improve quality of life in patients with gynecologic or breast cancer.
Conditions
- Anxiety Disorder
- Depression
- Fatigue
- Leydig Cell Tumor
- Ovarian Sarcoma
- Ovarian Stromal Cancer
- Pain
- Peritoneal Carcinomatosis
- Pseudomyxoma Peritonei
- Recurrent Breast Cancer
- Recurrent Cervical Cancer
- Recurrent Endometrial Carcinoma
- Recurrent Fallopian Tube Cancer
- Recurrent Gestational Trophoblastic Tumor
- Recurrent Ovarian Epithelial Cancer
- Recurrent Ovarian Germ Cell Tumor
- Recurrent Primary Peritoneal Cavity Cancer
- Recurrent Uterine Sarcoma
- Recurrent Vaginal Cancer
- Recurrent Vulvar Cancer
Interventions
- OTHER
-
questionnaire administration
Ancillary studies
- PROCEDURE
-
quality-of-life assessment
Patients will participate in a quality life assessment.
- PROCEDURE
-
psychosocial assessment and care
Participate in multi-component biobehavioral intervention
- BEHAVIORAL
-
behavioral intervention
Participate in multi-component biobehavioral intervention
- OTHER
-
cognitive intervention
A multi-component intervention based on cognitive and behavioral principles will be used. It combines effective intervention strategies selected for their relevance to patients with recurrent cancer.
- OTHER
-
educational intervention
Participate in multi-component biobehavioral intervention
Sponsors & Collaborators
-
National Cancer Institute (NCI)
collaborator NIH -
Ohio State University Comprehensive Cancer Center
lead OTHER
Principal Investigators
-
Barbara Andersen, PhD · Ohio State University Comprehensive Cancer Center
Study Design
- Allocation
- NA
- Purpose
- SUPPORTIVE_CARE
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 21 Years
- Max Age
- 85 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-10-31
- Primary Completion
- 2012-01-31
- Completion
- 2012-01-31
Countries
- United States
Study Locations
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