- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03136874
Motivations and Psychological Aspects of the Gametes' Donation (DonDon)
Study Overview
Status
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
Enrollment (Actual)
Contacts and Locations
Study Locations
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Paris, France, 75014
- CECOS Paris Cochin
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Paris, France, 75020
- CECOS Paris Tenon
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Alsace
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Schiltigheim, Alsace, France, 67303
- CECOS Alsace Strasbourg
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Aquitaine
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Bordeaux, Aquitaine, France, 33076
- CECOS Aquitaine Bordeaux
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Auvergne
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Clermont-Ferrand, Auvergne, France, 63003
- CECOS Auvergne Clermont-Ferrand
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Basse-Normandie
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Caen, Basse-Normandie, France, 14033
- CECOS Basse-Normandie Caen
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Bretagne
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Rennes, Bretagne, France, 35200
- CECOS Bretagne Rennes
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Centre
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Tours, Centre, France, 37000
- CECOS Centre Tours
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Champagne-ardenne
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Reims, Champagne-ardenne, France, 51092
- CECOS Champagne-ardenne
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Franche-Comté
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Besancon, Franche-Comté, France, 25030
- CECOS Franche-Comté
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Dijon, Franche-Comté, France, 21000
- CECOS Franche-Comté
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Languedoc-Roussillon
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Montpellier, Languedoc-Roussillon, France, 34295
- CECOS Languedoc-Roussillon Montpellier
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Lorraine
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Nancy, Lorraine, France, 54042
- CECOS Lorraine Nancy
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Midi-Pyrénées
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Toulouse, Midi-Pyrénées, France, 31059
- CECOS Midi-Pyrénées Toulouse
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Nord
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Lille, Nord, France, 59037
- CECOS Nord Lille
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Pays De La Loire
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Nantes, Pays De La Loire, France, 44093
- CECOS Pays de la Loire Nantes
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Picardie
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Amiens, Picardie, France, 80000
- CECOS Picardie
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Provence-Alpes-Côte d'Azur
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Marseille, Provence-Alpes-Côte d'Azur, France, 13385
- CECOS Provence-Alpes-Côte d'Azur Marseille
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Nice, Provence-Alpes-Côte d'Azur, France, 06202
- CECOS Provence-Alpes-Côte d'Azur
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Rhône-Alpes
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Lyon, Rhône-Alpes, France, 69677
- CECOS Rhône-Alpes Lyon
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Seine-Maritime
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Rouen, Seine-Maritime, France, 76031
- CECOS Rouen
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Seine-Saint-Denis
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Bondy, Seine-Saint-Denis, France, 93140
- CECOS Paris Jean Verdier
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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Donors who procreated
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Donors who don't procreated
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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
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Assessed by collecting questionnaire data and comparison between both groups of candidates.
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1 hour
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Assessment of the psychological profile of donors.
Time Frame: 4 months
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Profile comparison between candidates who have procreated and those who have not.
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4 months
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Assessment of the psychological profile of the donors and their motivations.
Time Frame: 4 months
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Links between their psychological profile and their motivations.
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4 months
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Assessment of the possibility of gametes preservation and donation motivations.
Time Frame: 4 months
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To understand links between the possibility of gametes preservation and donation motivations.
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4 months
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Assessment of the ethical aspects of donation.
Time Frame: 4 months
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Links between and the ethical aspects of donation and whether or not they have procreated.
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4 months
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Assessment of the ethical aspects of donation and personality questionnaires.
Time Frame: 4 months
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Links between the ethical aspects of donation and personality questionnaires.
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4 months
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Louis Bujan, Pr, CECOS Hôpital Paule de Viguier
Publications and helpful links
General Publications
- Ahuja KK, Mostyn BJ, Simons EG. Egg sharing and egg donation: attitudes of British egg donors and recipients. Hum Reprod. 1997 Dec;12(12):2845-52. doi: 10.1093/humrep/12.12.2845.
- Cauvin P. [Motivations of oocytes donors]. Gynecol Obstet Fertil. 2009 Nov-Dec;37(11-12):934-41. doi: 10.1016/j.gyobfe.2009.09.003. Epub 2009 Oct 12. French.
- Pennings G. Mirror gametes donation. J Psychosom Obstet Gynaecol. 2007 Dec;28(4):187-91. doi: 10.1080/01674820701656492.
- Sydsjo G, Lampic C, Brandstrom S, Gudmundsson J, Karlstrom PO, Solensten NG, Thurin-Kjellberg A, Svanberg AS. Personality characteristics in a Swedish national sample of identifiable oocyte donors. BJOG. 2011 Aug;118(9):1067-72. doi: 10.1111/j.1471-0528.2011.02953.x. Epub 2011 Apr 11.
- Sydsjo G, Lampic C, Brandstrom S, Gudmundsson J, Karlstrom PO, Solensten NG, Thurin-Kjellberg A, Skoog Svanberg A. Who becomes a sperm donor: personality characteristics in a national sample of identifiable donors. BJOG. 2012 Jan;119(1):33-9. doi: 10.1111/j.1471-0528.2011.03172.x. Epub 2011 Oct 18.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 13 6860 07
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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