Study of Information Received About Fertility and Infertility in Patients Who Have Finished Treatment for Cancer

The recruitment status of this study is unknown because the information has not been verified recently.
Verified February 2011 by National Cancer Institute (NCI).
Recruitment status was  Recruiting
Sponsor:
Information provided by:
National Cancer Institute (NCI)
ClinicalTrials.gov Identifier:
NCT01295463
First received: February 11, 2011
Last updated: August 9, 2013
Last verified: February 2011

February 11, 2011
August 9, 2013
December 2010
June 2012   (final data collection date for primary outcome measure)
  • Amount of information received on aspects of fertility and infertility [ Designated as safety issue: No ]
  • Relationship between demographic data, diagnosis, quality of life, and associated psychosocial information received [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01295463 on ClinicalTrials.gov Archive Site
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Study of Information Received About Fertility and Infertility in Patients Who Have Finished Treatment for Cancer
Descriptive Study to Evaluate the Information and Psychosocial Issues on the Risk on Infertility in Cancer Patients After Receiving Treatment in a Comprehensive Cancer Center

RATIONALE: Learning about the amount of information on fertility and infertility by patients before they received treatment for cancer in a comprehensive cancer center may help doctors plan the best treatment.

PURPOSE: This clinical trial is studying the amount of information on fertility and infertility received by patients before treatment of cancer in patients who have finished treatment.

OBJECTIVES:

Primary

  • To determine the amount of information received on aspects of fertility and infertility in patients with cancer prior to receiving treatment in a comprehensive cancer center.

Secondary

  • To analyze whether the information received by patients is related to the desire to be parents.
  • To analyze whether the information received by patients is related to the desire to be informed.
  • To determine whether there is a relationship between demographic data, diagnosis, quality of life, and associated psychosocial information received by patients.

OUTLINE: Patients complete questionnaires (Lickert and QLQ-C30) on the amount of information received prior to therapy and psychosocial issues on aspects of fertility and infertility once within 1-2 years after receiving treatment.

Observational
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Cancer
  • Other: questionnaire administration
  • Other: study of socioeconomic and demographic variables
  • Procedure: assessment of therapy complications
  • Procedure: fertility assessment and management
  • Procedure: psychosocial assessment and care
  • Procedure: quality-of-life assessment
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
96
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June 2012   (final data collection date for primary outcome measure)

DISEASE CHARACTERISTICS:

  • Diagnosis of breast cancer, germ cell tumor, colon cancer, leukemia, lymphoma, or sarcoma

    • Free of disease
  • Completed treatment within the past 1-2 years

PATIENT CHARACTERISTICS:

  • ECOG performance status 0-1
  • Must be able to read and self-complete study questionnaires
  • No psychological conditions that may prevent participation in the study

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • No concurrent treatment (hormonal treatment for breast cancer is allowed)
Both
18 Years to 45 Years
No
Spain
 
NCT01295463
ICO-FERTI, CDR0000695000, EU-21105
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Institut Catala D'Oncologia
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Principal Investigator: Josefina Rivera, RGN, MSN Institut Catala D'Oncologia
National Cancer Institute (NCI)
February 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP