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Discrimination, RacialVF-ADINNCT03646838

Family Experiences After International Adoption

An observational study of Discrimination, Racial, run by Centre Hospitalier St Anne at 4 sites in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to determine the types of experiences faced by families in France who have adopted a child internationally. In addition, internationally adopted adolescents are invited to respond to questions about their own personal experiences. Read more about this study

Who is it for?
Ages 11 years and olderHealthy volunteers can take part
Conditions the study is for
Discrimination, Racial
How many people
991 participants
Where
4 sitesFrance
Study dates
9 Oct 2017to 6 Jun 2018
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 11 years and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: Adoptive parents, regardless of the age of their children, as well as adolescents who have been adopted internationally, directly.

Who may be able to join

  • Parents :
  • Parents of an internationally adopted child, whose placement occurred at least 6 months ago
  • Willing and able to complete a questionnaire
  • Adolescents :
  • Internationally adopted adolescents who were placed at least 6 months ago
  • Willing and able to complete a questionnaire

Who cannot join

  • Parents :
  • 1. Unwilling or unable to complete the questionnaire
  • Adolescents :
  • Parents are unwilling for child to participate
  • Child is unwilling to participate
  • Unable to understand the questions

Trial locations and contacts

4 sites in 1 country.

France4 sites
  • Hospital Enfants CHU du BOCAGE

    Dijon

  • Hospital SAINTE ANNE

    Paris, 75014

  • Hospital NECKER

    Paris, 75015

  • Hospital MIGNOT

    Versailles, 78000

Other trials in France

About this study

The purpose of this study is to determine the types of experiences faced by families in France who have adopted a child internationally. In addition, internationally adopted adolescents are invited to respond to questions about their own personal experiences.

Read the detailed description

Microaggressions, or "unintended discrimination" related to adoption have been widely investigated in the USA. These microaggressions may relate to both adoptive status and country of origin, or both. However, the prevalence and qualitative characteristics of these events have been seldom studied in other countries. Differences in cultural norms and practices among countries might influence the type and frequency of microaggressions experienced by adopted children and their families. Brief anonymous questionnaires devised to elicit personal experiences related to microaggressions will be distributed by 4 clinical services serving this population (3 pediatric, 1 child psychiatric) and by 2 large adoptive family support networks to adoptive parents in France. Frequencies and relations between experience of micro-aggressions and other variables will be analyzed.

Keywords
International adoption, Family experiences, Adolescents, France
Medical subject headings
Racism

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number and type of micro-aggressions experienced by French families who have adopted internationally

    Parents will respond to a questionnaire regarding their experiences of micro-aggressions as an adoptive family in France, enumerating the types of discrimination (if any) they have encountered, in what context or environment this occurred, and their feelings in response to these experiences. The types of micro-aggressions could include hearing derogatory comments about adoption in general, their child's country of origin or appearance, etc. Parents may also experience well-meaning but uninformed comments ("how much did she cost?") which are also experienced as micro-aggressions. Simple frequency statistics enumerating these experiences will be compiled. These will be compared to basic demographic indicators such as the country of origin of the child, the child's age at adoption, the child's current age, the time interval since adoption, etc.

    Measured: parents respond to a questionnaire at a single time point, regarding their experience. Participation is hence limited to the 30 minutes required to complete the questionnaire.

Secondary outcomes (1)
  1. Number and type of micro-aggressions experienced by internationally adopted adolescents in France

    Adolescents will respond to a questionnaire regarding their experiences of micro-aggressions as adopted individuals in France, enumerating the types of discrimination (if any) they have encountered, in what context or environment this occurred, and their feelings in response to these experiences. The types of micro-aggressions could include hearing derogatory comments about adoption in general, their country of origin or appearance, etc. Adolescents may also experience well-meaning but uninformed comments ("why did your real parents abandon you?") which are also experienced as micro-aggressions. Simple frequency statistics enumerating these experiences will be compiled. These will be compared to basic demographic indicators such as their country of origin, their age at adoption, their current age, the time interval since adoption, etc.

    Measured: Adolescents respond to a questionnaire at a single time point, regarding their experiences as an adopted person in France. Participation is hence limited to the 30 minutes required to complete the questionnaire.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Aug 2018
  2. Study start9 Oct 2017
  3. Primary completion6 Jun 2018
  4. Study completion6 Jun 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
991 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03646838
Sponsor's protocol ID
D17-P16
Acronym
VF-ADIN
Status last verified
Jul 2024
First submitted
20 Mar 2018
Last updated
11 Jul 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Frable DE, Wortman C, Joseph J. Predicting self-esteem, well-being, and distress in a cohort of gay men: the importance of cultural stigma, personal visibility, community networks, and positive identity. J Pers. 1997 Sep;65(3):599-624. doi: 10.1111/j.1467-6494.1997.tb00328.x.

    PubMed 9327589
  • Sue DW, Capodilupo CM, Torino GC, Bucceri JM, Holder AM, Nadal KL, Esquilin M. Racial microaggressions in everyday life: implications for clinical practice. Am Psychol. 2007 May-Jun;62(4):271-86. doi: 10.1037/0003-066X.62.4.271.

    PubMed 17516773

Questions about this trial

What is this clinical trial studying?

An observational study of Discrimination, Racial, run by Centre Hospitalier St Anne at 4 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Jul 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 4 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number and type of micro-aggressions experienced by French families who have adopted internationally (time frame: parents respond to a questionnaire at a single time point, regarding their experience. Participation is hence limited to the 30 minutes required to complete the questionnaire.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03646838, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Jul 2024.

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