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Utvidelse av studien om barndomsforhold til romantiske forhold til unge voksne

Dannelsen av sunne, stabile romantiske forhold i ung voksen alder: et utviklingsmessig og dyadisk perspektiv

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.

Studieoversikt

Status

Fullført

Forhold

Detaljert beskrivelse

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.

Studietype

Observasjonsmessig

Registrering (Faktiske)

259

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Maryland
      • Bethesda, Maryland, Forente stater, 20892
        • National Institute of Child Health and Human Development (NICHD), 9000 Rockville

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 30 år (Voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

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.

Beskrivelse

  • 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.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Observasjonsmodeller: COHORT
  • Tidsperspektiver: PROSPECTIVE

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Romantic Relationship Quality
Tidsramme: Ongoing

Romantic Relationship Quality

Ongoing

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

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

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

29. mai 2013

Primær fullføring (Faktiske)

15. august 2019

Datoer for studieregistrering

Først innsendt

29. mai 2013

Først innsendt som oppfylte QC-kriteriene

29. mai 2013

Først lagt ut (Antatt)

3. juni 2013

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

8. oktober 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

7. oktober 2026

Sist bekreftet

22. september 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 999913113
  • 13-CH-N113

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

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.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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