Motivations and Psychological Aspects of the Gametes' Donation (DonDon)

July 15, 2019 updated by: University Hospital, Toulouse
The main objective is to study donors' personality and motivations characteristics of the different recruitment methods and thus to answer questions related to the donation's approach, its representations as well as motivations and the profile of the donors.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The methodology used is mixed with a quantitative and qualitative approach. The first one is a psychosocial approach with two groups: donors of gametes without children, and donors who have already procreated. Two questionnaires will be used in this survey. The first aims to study the donors' socio-personal characteristics and motivations. The latter studies donors' personality traits.

The second approach is qualitative by a clinical case study. It is a psycho-dynamic approach, taking into consideration the donor (men and women), with all their subjectivity, their personal and family history and their representations.

Study Type

Observational

Enrollment (Actual)

1002

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Paris, France, 75014
        • CECOS Paris Cochin
      • Paris, France, 75020
        • CECOS Paris Tenon
    • Alsace
      • Schiltigheim, Alsace, France, 67303
        • CECOS Alsace Strasbourg
    • Aquitaine
      • Bordeaux, Aquitaine, France, 33076
        • CECOS Aquitaine Bordeaux
    • Auvergne
      • Clermont-Ferrand, Auvergne, France, 63003
        • CECOS Auvergne Clermont-Ferrand
    • Basse-Normandie
      • Caen, Basse-Normandie, France, 14033
        • CECOS Basse-Normandie Caen
    • Bretagne
      • Rennes, Bretagne, France, 35200
        • CECOS Bretagne Rennes
    • Centre
      • Tours, Centre, France, 37000
        • CECOS Centre Tours
    • Champagne-ardenne
      • Reims, Champagne-ardenne, France, 51092
        • CECOS Champagne-ardenne
    • Franche-Comté
      • Besancon, Franche-Comté, France, 25030
        • CECOS Franche-Comté
      • Dijon, Franche-Comté, France, 21000
        • CECOS Franche-Comté
    • Languedoc-Roussillon
      • Montpellier, Languedoc-Roussillon, France, 34295
        • CECOS Languedoc-Roussillon Montpellier
    • Lorraine
      • Nancy, Lorraine, France, 54042
        • CECOS Lorraine Nancy
    • Midi-Pyrénées
      • Toulouse, Midi-Pyrénées, France, 31059
        • CECOS Midi-Pyrénées Toulouse
    • Nord
      • Lille, Nord, France, 59037
        • CECOS Nord Lille
    • Pays De La Loire
      • Nantes, Pays De La Loire, France, 44093
        • CECOS Pays de la Loire Nantes
    • Picardie
      • Amiens, Picardie, France, 80000
        • CECOS Picardie
    • Provence-Alpes-Côte d'Azur
      • Marseille, Provence-Alpes-Côte d'Azur, France, 13385
        • CECOS Provence-Alpes-Côte d'Azur Marseille
      • Nice, Provence-Alpes-Côte d'Azur, France, 06202
        • CECOS Provence-Alpes-Côte d'Azur
    • Rhône-Alpes
      • Lyon, Rhône-Alpes, France, 69677
        • CECOS Rhône-Alpes Lyon
    • Seine-Maritime
      • Rouen, Seine-Maritime, France, 76031
        • CECOS Rouen
    • Seine-Saint-Denis
      • Bondy, Seine-Saint-Denis, France, 93140
        • CECOS Paris Jean Verdier

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 45 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Volonteers are recruted in the different CECOS. These subjects (who have already procreated, or not) are going to donate sperm/egg.

Description

Inclusion Criteria:

  • Candidates for gametes donation
  • Less than 45 years for men
  • Less than 37 years for women
  • Affiliation to social service

Exclusion Criteria:

  • Under guardianship, or trusteeship

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Donors who procreated
  • Quantitative method : Two questionnaires will be used to define sociodemographic data, motivations and personality traits of donors.
  • Qualitative method : Clinical interviewing allows data collection adapted to study the motivations of sperm/egg donors, their representations, the experience and the inscription of the donation in their personal stories.
Donors who don't procreated
  • Quantitative method : Two questionnaires will be used to define sociodemographic data, motivations and personality traits of donors.
  • Qualitative method : Clinical interviewing allows data collection adapted to study the motivations of sperm/egg donors, their representations, the experience and the inscription of the donation in their personal stories.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessment of motivations of candidates who have procreated and those who have not procreated.
Time Frame: 1 hour
Assessed by collecting questionnaire data and comparison between both groups of candidates.
1 hour

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessment of the psychological profile of donors.
Time Frame: 4 months
Profile comparison between candidates who have procreated and those who have not.
4 months
Assessment of the psychological profile of the donors and their motivations.
Time Frame: 4 months
Links between their psychological profile and their motivations.
4 months
Assessment of the possibility of gametes preservation and donation motivations.
Time Frame: 4 months
To understand links between the possibility of gametes preservation and donation motivations.
4 months
Assessment of the ethical aspects of donation.
Time Frame: 4 months
Links between and the ethical aspects of donation and whether or not they have procreated.
4 months
Assessment of the ethical aspects of donation and personality questionnaires.
Time Frame: 4 months
Links between the ethical aspects of donation and personality questionnaires.
4 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Louis Bujan, Pr, CECOS Hôpital Paule de Viguier

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2016

Primary Completion (Actual)

March 1, 2019

Study Completion (Actual)

March 1, 2019

Study Registration Dates

First Submitted

March 3, 2017

First Submitted That Met QC Criteria

April 26, 2017

First Posted (Actual)

May 2, 2017

Study Record Updates

Last Update Posted (Actual)

July 16, 2019

Last Update Submitted That Met QC Criteria

July 15, 2019

Last Verified

July 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 13 6860 07

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Gametes Donors

Clinical Trials on Interview and questionaires

3
Subscribe