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

NCT ID: NCT01295463

Last Updated: 2013-08-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

96 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-12-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Cancer

Keywords

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sexual dysfunction psychosocial effects of cancer and its treatment infertility colon cancer male breast cancer breast cancer germ cell tumor ovarian sarcoma uterine sarcoma chronic lymphocytic leukemia osteosarcoma chronic myelogenous leukemia non-Hodgkin lymphoma adult acute myeloid leukemia with 11q23 (MLL) abnormalities adult acute myeloid leukemia with inv(16)(p13;q22) adult acute myeloid leukemia with t(15;17)(q22;q12) adult acute myeloid leukemia with t(16;16)(p13;q22) adult acute myeloid leukemia with t(8;21)(q22;q22) mast cell leukemia hairy cell leukemia prolymphocytic leukemia adult acute lymphoblastic leukemia adult acute myeloid leukemia adult Hodgkin lymphoma adult T-cell leukemia/lymphoma small intestine lymphoma anaplastic large cell lymphoma angioimmunoblastic T-cell lymphoma mycosis fungoides/Sezary syndrome intraocular lymphoma primary central nervous system non-Hodgkin lymphoma primary central nervous system Hodgkin lymphoma noncutaneous extranodal lymphoma secondary acute myeloid leukemia acute undifferentiated leukemia central nervous system leukemia T-cell large granular lymphocyte leukemia atypical chronic myeloid leukemia, BCR-ABL1 negative clear cell sarcoma of the kidney Kaposi sarcoma adult soft tissue sarcoma chronic myelomonocytic leukemia secondary central nervous system Hodgkin lymphoma cutaneous lymphoma adult non-Hodgkin lymphoma

Interventions

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questionnaire administration

Intervention Type OTHER

study of socioeconomic and demographic variables

Intervention Type OTHER

assessment of therapy complications

Intervention Type PROCEDURE

fertility assessment and management

Intervention Type PROCEDURE

psychosocial assessment and care

Intervention Type PROCEDURE

quality-of-life assessment

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

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)
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Institut Català d'Oncologia

OTHER

Sponsor Role lead

Principal Investigators

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Josefina Rivera, RGN, MSN

Role: PRINCIPAL_INVESTIGATOR

Institut Català d'Oncologia

Locations

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Institut Catala D'Oncologia

L'Hospitalet de Llobregat, , Spain

Site Status RECRUITING

Countries

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Spain

Facility Contacts

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Josefina Rivera, RGN, MSN

Role: primary

Other Identifiers

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CDR0000695000

Identifier Type: REGISTRY

Identifier Source: secondary_id

EU-21105

Identifier Type: -

Identifier Source: secondary_id

ICO-FERTI

Identifier Type: -

Identifier Source: org_study_id