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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

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