Biobehavioral and Sociodemographic Characteristics of Long Term Survivors of Ovarian Cancer
3 other identifiers
observational
240
1 country
5
Brief Summary
The goal of this research study is to learn about diet and exercise habits, emotions, and social support in the lives of women with ovarian cancer.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2014
Longer than P75 for all trials
5 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 16, 2014
CompletedStudy Start
First participant enrolled
January 16, 2014
CompletedFirst Posted
Study publicly available on registry
January 23, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 30, 2026
April 15, 2026
April 1, 2026
13 years
January 16, 2014
April 10, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Biobehavioral Information Collection in Ovarian Cancer Survivors
Biobehavioral information collected regarding social support, depressed mood, life stress, quality of life, meaning in life, socioeconomic and relationship status, and lifestyle factors such as exercise and diet, which have been linked with cancer progression and/or survival in cancer patients.
1 day
Study Arms (1)
Ovarian Cancer Survivors
Short-term and long-term ovarian cancer survivors
Interventions
Questionnaire completion asking questions about quality of life, mood, social support, stress, diet, lifestyle, and demographic information. Questionnaire should take about 60-90 minutes to complete.
Interview asking questions about the amount of stress participant may be having or have had in the past. It should take about 25-30 minutes to complete the interview.
Eligibility Criteria
Long term and short term ovarian cancer survivors at the University of Texas MD Anderson Cancer Center in Houston, Texas
You may qualify if:
- For the long-term survivor group: alive for at least seven years post-diagnosis.
- At least 18 years of age.
- Can speak and read English.
- diagnosed with stage III-IV ovarian, peritoneal or fallopian tube cancer
You may not qualify if:
- Are in hospice or about to be referred to hospice within the next 3-6 weeks.
- Are not oriented to time, person, or place.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- M.D. Anderson Cancer Centerlead
- United States Department of Defensecollaborator
Study Sites (5)
Cedars Sinai
West Hollywood, California, 90048, United States
University of Iowa
Iowa City, Iowa, 52242, United States
Memorial Sloan Kettering
New York, New York, 10065, United States
University of Oklahoma
Norman, Oklahoma, 73019, United States
University of Texas MD Anderson Cancer Center
Houston, Texas, 77030, United States
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Eileen H. Shinn, PHD, MS, BA
M.D. Anderson Cancer Center
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 16, 2014
First Posted
January 23, 2014
Study Start
January 16, 2014
Primary Completion (Estimated)
December 30, 2026
Study Completion (Estimated)
December 30, 2026
Last Updated
April 15, 2026
Record last verified: 2026-04