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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02630641
Other study ID # A-54-52014-218
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2015
Est. completion date November 2017

Study information

Verified date May 2023
Source Ipsen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The general hypothesis put forward in this study is that the degree of cohesion (agreement) in the relationship, or dyadic adjustment affects a patient's quality of life and clinical course during the first few critical months following diagnosis and the introduction of treatment. The level of cohesion in the relationship is certainly not the only parameter associated with changes in the quality of life. Other factors must also be investigated such as level of education, circumstances surrounding the diagnosis (new diagnosis or relapse), management (single therapy or adjuvant therapy), the level of physical activity, the patient's age and the presence of functional disorders, etc.


Recruitment information / eligibility

Status Completed
Enrollment 1000
Est. completion date November 2017
Est. primary completion date November 2017
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient presenting with histologically confirmed prostate cancer. - Patient eligible to start GnRH agonist therapy, either as monotherapy or adjuvant therapy, and for whom one of these treatments was selected voluntarily by the urologist, prior to the start of the study. - Patient currently living with the same partner for at least 6 months. - Patient and partner capable of reading, understanding and returning an evaluation self-questionnaire 6 months after the initial consultation. - Patient giving its written consent to participate to the study. Exclusion Criteria: - The subject is participating in another clinical trial. - Patient who has received a GnRH agonist therapy during the last 2 years.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Gonadotropin-releasing Hormone (GnRH) agonist therapy
This is a non-interventional study. Thus, investigators are free to choose GnRH agonist therapy product, and modalities of administration in accordance with local Summary of Product Characteristics.

Locations

Country Name City State
France Ipsen Central Contact Paris

Sponsors (1)

Lead Sponsor Collaborator
Ipsen

Country where clinical trial is conducted

France, 

References & Publications (1)

Droupy S, Colson MH, Pello-Leprince-Ringuet N, Perrot V, Descazeaud A. EQUINOXE study: Impact of relational cohesion and sexuality on the quality of life of patients treated with gonadotropin-releasing hormone agonist for prostate cancer. BJUI Compass. 20 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in quality of life of the patient. Assessment of the dyadic adjustment and its impact on the quality of life of the patient through self-questionnaire by the patient and the partner Baseline and 6 months
Secondary Assessment of representations of illness Self-questionnaire by the patient and the partner Baseline
Secondary Correlations between quality of life specific to prostate cancer, general quality of life and dyadic adjustment. Self-questionnaire by the patient only 6 months
Secondary Proportion of couples with a consistency or inconsistency level of dyadic adjustment 6 months
Secondary Investigation of factors associated with patient's perception of dyadic adjustment on changes quality of life Self-questionnaire by the patient and the partner Baseline and 6 months
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