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Extension de l'étude sur les relations d'enfance aux relations amoureuses des jeunes adultes

La formation de relations amoureuses saines et stables à l'âge adulte : une perspective développementale et dyadique

Background:

- An earlier study on child development focused on the relationship between children and their caregivers (usually mothers). It looked at how this relationship influenced children's social and mental development. It also studied how these children related with family members and friends. Researchers are now interested in expanding the study with the same group of children. They want to look at these children, who are now young adults, and focus on their current romantic relationships. This new study will look at how child development affects the formation of stable, mature romantic relationships in young adulthood. Original child study participants and their significant others will be included in the new study. Only participants who are living together with a partner will be studied.

Objectives:

- To look at romantic partnerships in a childhood study s original participants and their significant others.

Eligibility:

  • Participants of the 88-CH-32 study who are at least 18 years of age.
  • Significant others of the study participants who are at least 18 years of age.
  • Original participants and significant others must be cohabiting (living together).

Design:

  • No screening tests will be required for this study. No study visits will be needed. Samples will not be collected.
  • Original study participants will fill out four online questionnaires. They will be on a National Institute of Child Health and Human Development (NICHHD) website. They will ask personal questions about relationships with the current romantic partner and other important people. The questions will take about 25 minutes to answer.
  • Significant others will fill out 13 online questionnaires. They will be on a NICHHD website. They will ask personal questions about the romantic partner and other important people. The questions will take about 1.5 hours to answer.
  • All participants will receive a small amount of money for completing the study.

Aperçu de l'étude

Statut

Complété

Les conditions

Description détaillée

The purpose of this study is to expand our ongoing longitudinal study (study 88-CH-32) by gathering information about romantic partnerships from both the longitudinal study s now young adult target children, who were 5 months old when the study began and are now as old as 23 years of age, and their significant others. Because the target children are approaching the age when they form lasting romantic relationships, we wish to track these partnerships as they form. With these data, we will be uniquely suited to identify how key individual and inter-personal factors at distinct points of development (i.e., childhood, adolescence, and young adulthood) influence the formation of stable, emotionally intimate, mutually dependent romantic relationships during young adulthood. In particular, we aim to disentangle the influence of childhood and adolescent interpersonal experiences in other relational spheres (i.e., relationships with parents and friends) from the influence of contemporary characteristics of both members of the romantic dyad. As part of our examination, in addition to relationship quality, we focus on the strength of each dyad member s attachment to his or her parents as well as each other, thereby allowing for the examination of attachment transfer, an important yet understudied characteristic of successful romantic relationship formation.

Only cohabiting (whether married or otherwise) young-adult romantic dyads that include a target child from our existing longitudinal study (dyad N equals 250; 500 young adults overall, all volunteers) will be eligible to participate in this new data collection. By limiting eligibility in this way, we will have data extending back to infancy for one member of each young-adult romantic dyad. All data collected will be collected via a secure, password-protected website.

As part of our on-going longitudinal study, we already collected (or will collect) individual information from the young adult target children (mental health, attachment style, attachment strength, personality, substance use). We propose here to collect complementary individual information from the significant others of young adult target children as well as dyad-level information (relationship satisfaction and household functioning) from both members of the cohabiting romantic dyad. Combined with existing data from our longitudinal study, these new data will enable us to move beyond most current research focused on the developmental antecedents of successful young adult romantic relationships and examine how an individual s past interpersonal experiences interplay with the contemporary characteristics of both young-adult romantic dyad members to influence the state of the romantic dyad.

Type d'étude

Observationnel

Inscription (Réel)

259

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Maryland
      • Bethesda, Maryland, États-Unis, 20892
        • National Institute of Child Health and Human Development (NICHD), 9000 Rockville

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 30 ans (Adulte)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

Méthode d'échantillonnage

Échantillon non probabiliste

Population étudiée

Original child (now adult) study participants from protocol 88-CH-0032 and their significant others will be included in the new study. Only participants who are living together with a partner will be studied.

La description

  • INCLUSION AND EXCLUSION CRITERIA:

Among the young adult target children from study 88-CH-32 (N = 250), those with significant others are eligible to participate in this study, as are their significant others. However if a target child s significant other is a minor (i.e., under the age of 18), that significant other will not be eligible to participate.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Modèles d'observation: COHORT
  • Perspectives temporelles: PROSPECTIVE

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Romantic Relationship Quality
Délai: Ongoing

Romantic Relationship Quality

Ongoing

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Diane L Putnick, Ph.D., Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

29 mai 2013

Achèvement primaire (Réel)

15 août 2019

Dates d'inscription aux études

Première soumission

29 mai 2013

Première soumission répondant aux critères de contrôle qualité

29 mai 2013

Première publication (Estimé)

3 juin 2013

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

8 octobre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

7 octobre 2026

Dernière vérification

22 septembre 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • 999913113
  • 13-CH-N113

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

All data will be stored permanently in an archival database by the National Institutes of Health. No one other than members of the research team will have access to the data without the explicit consent of the volunteer adult.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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