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Parents With Bipolar Disorder: Relationship of Adaptation to Own Illness With Risk Perception and Coping With Perceived Risk to a Child

Background:

  • Bipolar disorder is a common mood disorder that affects 1% to 2% of the population. Individuals with bipolar disorder tend to have periods of mania that are characterized by extra energy, very poor judgment or unrealistic beliefs about their thoughts and abilities, and an inability to complete thoughts and tasks; as well as major depressive episodes. The range and frequency of symptoms in affected individuals can vary greatly. Most individuals have cyclical symptoms and spend more time in a normal mood state than in an overtly symptomatic state.
  • Relatives of individuals with bipolar disorder have an increased risk for bipolar disorder and other mood disorders. Currently, risk assessment for recurrence of a mood disorder is based on family and medical histories; genetic testing has not proved particularly useful to date for assessing risks of a mood disorder.
  • Despite its prevalence, there is limited research on coping with bipolar illness. No published studies have examined adaptation to living with bipolar disorder or risk for bipolar disorder. More specifically, though a positive family history is the most important known risk factor for bipolar disorder, there are no published studies about response to the threat of future illness onset in children, risk modification efforts undertaken by affected parents, or coping with the risk for illness in children.

Objectives:

  • To examine parents appraisals of the impact and cause of bipolar disorder, and the association with their perceived risk for bipolar illness in their child and how they cope with their perception of risk to their child.
  • To assess whether parents adaptation to their own illness is associated with coping with perceived risk to their child.
  • To describe parents coping strategies related to perceived risk in their children.

Eligibility:

- Men and women at least 18 years of age who have been diagnosed with bipolar disorder and who have at least one biological child (30 years of age or younger). Participants must be a primary caregiver for their children.

Design:

  • Participants in this study will take an online survey and answer questions about disease perceptions, coping strategies, and adapting to a diagnosis of bipolar disorder, addressing issues such as the following:
  • Assessing the threat of bipolar disorder and coping with one s own illness.
  • Optimism/pessimism of the individual coping with the illness.
  • Perception of risk to a child, and coping with the perceived risk.
  • Data from this study will not be shared with the participants/respondents.

Studieöversikt

Status

Avslutad

Betingelser

Detaljerad beskrivning

Though psychiatric disorders are extremely common and individuals with bipolar disorder have reproductive fitness approaching population rates, we know very little about the perceptions and coping of parents with bipolar disorder related to their at-risk children. Bipolar disorder is an etiologically-complex psychiatric disorder that is caused by a combination of genetic and environmental risk factors. This study proposes to assess perceptions of parents with bipolar disorder about their illness, response to illness threat, and concerns about their children s risks. We then propose to assess whether those appraisals are associated with the outcomes of coping strategies and adaption. As informed by the Transactional Theory of Stress and Coping, we propose to use a web-based survey to examine disease perceptions, coping strategies, and adaptation to the disorder. Respondents will be recruited through the National Alliance of the Mentally Ill (NAMI). The study is cross-sectional and the survey is composed of several valid and reliable scales to measure the constructs predicted to be involved in adaptation. Open-ended questions are included to help interpret results from the measures. Knowledge about parents perceptions and coping with their own illness and with risk to children may lead to studies of potential coping interventions. Ultimately, downstream studies may help to improve parents adaptation to their own condition and how successfully they are able to manage concerns about perceived risks to their child.

Studietyp

Observationell

Inskrivning (Faktisk)

266

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Maryland
      • Bethesda, Maryland, Förenta staterna, 20892
        • National Human Genome Research Institute (NHGRI), 9000 Rockville Pike
      • Bethesda, Maryland, Förenta staterna
        • NAMI Research Institute

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 90 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

  • INCLUSION CRITERIA:
  • Have a diagnosis of bipolar disorder
  • Be 18 years or older
  • Be a biological parent of a child who is younger than 30 years old
  • Be willing to participate in the survey
  • The participant must be (or must have been) the primary caretaker for his or her child.

EXCLUSION CRITERIA:

  • A participant must meet inclusion criteria.
  • A participant s child cannot have been diagnosed with a mood disorder or other serious psychiatric disorder.
  • A participant s child cannot have been adopted.
  • The participant s child cannot be 30 years of age or older.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Vad mäter studien?

Primära resultatmått

Resultatmått
Adaptation to bipolar disorder.

Sekundära resultatmått

Resultatmått
Coping with perceived risk of bipolar to ones children.

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

23 oktober 2009

Avslutad studie

7 juni 2013

Studieregistreringsdatum

Först inskickad

10 november 2009

Först inskickad som uppfyllde QC-kriterierna

10 november 2009

Första postat (Uppskatta)

11 november 2009

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

5 april 2018

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

4 april 2018

Senast verifierad

7 juni 2013

Mer information

Termer relaterade till denna studie

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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