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Trial Title:
A Controlled Study of Quality of Life and it's Related Factors Among Gynecological Cancer Survivors
NCT ID:
NCT01187706
Condition:
Cervical Cancer
Ovarian Cancer
Endometrial Cancer
Conditions: Official terms:
Endometrial Neoplasms
Conditions: Keywords:
gynecological cancer survivors
quality of life
Study type:
Observational
Overall status:
Unknown status
Study design:
Time perspective:
Cross-Sectional
Summary:
To compare quality of life and it's related factors between gynecological cancer survivor
and healthy controls.
Detailed description:
This study used a cross-sectional design. By using the method of purposive sampling, the
70 gynecological cancer patients who had completed the active treatments for six months
will be recruited from the oncology and gynecology clinics of a medical center in the
Northern Taiwan area. The 70 healthy controls without any cancer will be recruited from
clinic and from friends and colleagues. The instruments include "Sample characteristics
questionnaire," "Short Form-12 (SF-12)," "Medical Outcome Study Sleep Scale (MOS-sleep),"
"Beck Depression Inventory-II (BDI)," "State-Trait Anxiety Inventory (STAI)," "Sexual
Activity Questionnaire (SAQ), and "The Experiences in Close Relationships-Revised
(ECR-R)." The data will be analyzed by descriptive statistical analysis, independent
t-test, ANOVA, Scheffe's test, Pearson's correlation, and stepwise regression.
Criteria for eligibility:
Study pop:
This study used a cross-sectional design. By using the method of purposive sampling, the
70 gynecological cancer patients who had completed the active treatments for six months
will be recruited from the oncology and gynecology clinics of a medical center in the
Northern Taiwan area. The 70 healthy controls without any cancer will be recruited from
clinic and from friends and colleagues.
Sampling method:
Non-Probability Sample
Criteria:
Inclusion Criteria:
- Been diagnosed as cervical cancer, ovarian cancer or endometrial cancer, and has
completed six months after the relevant treatment.
- 20-70 years old
- Agreed to participate in this study.
Exclusion Criteria:
- Combined with other non-gynecologic cancer (cervical cancer, ovarian cancer or
endometrial cancer) patients.
Gender:
Female
Minimum age:
20 Years
Maximum age:
70 Years
Healthy volunteers:
Accepts Healthy Volunteers
Locations:
Facility:
Name:
National Taiwan University Hospital
Address:
City:
Taipei
Zip:
100
Country:
Taiwan
Status:
Recruiting
Contact:
Last name:
Fei-Hsiu Hsiao, Ph.D.
Phone:
+886-2-23123456
Phone ext:
88432
Email:
hsiaofei@ntu.edu.tw
Start date:
August 2010
Lead sponsor:
Agency:
National Taiwan University Hospital
Agency class:
Other
Source:
National Taiwan University Hospital
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT01187706
