The Experience of Uncertainty in Parents of Children With an Undiagnosed Medical Condition
NCT ID: NCT00955370
Last Updated: 2017-07-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
500 participants
OBSERVATIONAL
2009-08-04
2012-04-10
Brief Summary
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* Rare and undiagnosed conditions are often chronic and disabling, with symptoms affecting different organ systems at various levels of severity. Perhaps the most challenging feature of an undiagnosed medical condition that has lasted 2 or more years is its characteristic uncertainty. In the absence of a diagnosis, health care professionals can provide only limited treatment and prognostic information.
* In the case of a child with an undiagnosed condition, the uncertainty that accompanies what is often a chronic, debilitating medical condition and an undefined prognosis may have physical, psychological, social, and spiritual implications for the entire family. Research suggests that parents of a child with an undiagnosed medical condition may be at significantly increased risk of anxiety, depression, poor health, and overall lower quality of life.
* It is not well understood how individuals cope with and adapt to chronic uncertainty, and the factors that influence this process. To design future interventions, descriptive studies are needed to reveal predictors that can be manipulated to improve outcomes.
Objectives:
* To examine whether perceptions of uncertainty, and perceived personal control, are associated with coping and adaptation.
* To examine how the length of time elapsed since child was identified as sick and perceptions of uncertainty affect coping and adaptation.
* To assess how perceptions of uncertainty, time elapsed since child became sick, optimism, and perceived personal control affect coping and adaptation.
Eligibility:
* Parents (older than 18 years of age) of children who have an undiagnosed medical condition.
* Participants must have a working e-mail address or fixed postal address.
Design:
* Parents will be recruited from Web-based support networks for parents of undiagnosed children through Web site postings, electronic mailing lists, and printed newsletter postings.
* Participants will be asked to complete a questionnaire about their experiences in living with a child who has an undiagnosed but chronic medical condition. The main outcome variable is adaptation to living with one's child's undiagnosed medical condition.
* Participants have the option to complete an online or paper version of the questionnaire. The questionnaire should take between 20 and 30 minutes to complete.
* No medical treatments are specifically offered as a part of this study.
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Detailed Description
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Conditions
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Study Design
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RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Biological or adoptive parent
* At least one child of participants has a medical problem or problems that have remained undiagnosed for \> 2 years
* The child with an undiagnosed medical problem must reside with the parent
* Read and write in English
Exclusion Criteria
18 Years
100 Years
ALL
No
Sponsors
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National Human Genome Research Institute (NHGRI)
NIH
Principal Investigators
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Barbara B Biesecker
Role: PRINCIPAL_INVESTIGATOR
National Human Genome Research Institute (NHGRI)
Locations
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National Human Genome Research Institute (NHGRI), 9000 Rockville Pike
Bethesda, Maryland, United States
Countries
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References
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Guillem P, Cans C, Robert-Gnansia E, Ayme S, Jouk PS. Rare diseases in disabled children: an epidemiological survey. Arch Dis Child. 2008 Feb;93(2):115-8. doi: 10.1136/adc.2006.104455. Epub 2007 Oct 17.
Lenhard W, Breitenbach E, Ebert H, Schindelhauer-Deutscher HJ, Henn W. Psychological benefit of diagnostic certainty for mothers of children with disabilities: lessons from Down syndrome. Am J Med Genet A. 2005 Mar 1;133A(2):170-5. doi: 10.1002/ajmg.a.30571.
Rosenthal ET, Biesecker LG, Biesecker BB. Parental attitudes toward a diagnosis in children with unidentified multiple congenital anomaly syndromes. Am J Med Genet. 2001 Oct 1;103(2):106-14. doi: 10.1002/ajmg.1527.
Other Identifiers
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09-HG-N206
Identifier Type: -
Identifier Source: secondary_id
999909206
Identifier Type: -
Identifier Source: org_study_id
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