Support of the Sexual Health in Oncology

Sponsor

Groupe Hospitalier Paris Saint Joseph (Other)

Overall Status

Withdrawn

CT.gov ID

NCT03166774

Collaborator

(none)

Enrollment

Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

Implementation of sexual health support program in oncology department. This program is organized in 3 axes. One is to inform the side effects of treatment on sexual health.

There is a counselling team (nurse, esthetician,sexologue..etc) to raise the subject with patient and partner .

Finally, the oncologist continue during the treatment to evaluate the benefit of this program and adapt their counselling according to the needs

Condition or Disease	Intervention/Treatment	Phase
Oncology Sexual Health	Other: Program of support of the sexual health

Study Design

Study Type:

Observational

Actual Enrollment :

0 participants

Observational Model:

Cohort

Time Perspective:

Prospective

Official Title:

Support of the Sexual Health in Oncology

Actual Study Start Date :

Jun 6, 2016

Actual Primary Completion Date :

Jun 6, 2017

Anticipated Study Completion Date :

Jun 6, 2017

Arms and Interventions

Arm	Intervention/Treatment
patient consulting in oncology ervice Program of support of the sexual health in oncology by questionnaire	Other: Program of support of the sexual health Patients included in the study have to answer to a questionnaire

Arm

Intervention/Treatment

patient consulting in oncology ervice

Program of support of the sexual health in oncology by questionnaire

Other: Program of support of the sexual health

Patients included in the study have to answer to a questionnaire

Outcome Measures

Primary Outcome Measures

Benefit of the care measurement program [Day 1]
assessment of data recorded on questionnaire

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

all patient consulting in oncology service
age > 18 years
accepting to participate

Exclusion Criteria:

Age< 18 years
Refusing to participate

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

Groupe Hospitalier Paris Saint Joseph

Investigators

Principal Investigator: Alexandra SCHULTZ, Psychologist, Groupe Hospitalier Paris Saint Joseph

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Groupe Hospitalier Paris Saint Joseph

ClinicalTrials.gov Identifier:

NCT03166774

Other Study ID Numbers:

AssO

First Posted:

May 25, 2017

Last Update Posted:

Aug 9, 2018

Last Verified:

Aug 1, 2018

Individual Participant Data (IPD) Sharing Statement:

Plan to Share IPD:

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Additional relevant MeSH terms:

Neoplasms

Study Results

No Results Posted as of Aug 9, 2018