Stress, Psychological Clinical Trial
Official title:
Impact of Early Intervention on Maternal Stress in Mothers of Fetuses Diagnosed With Single Ventricle Physiology Requiring Neonatal Surgery
Verified date | April 2017 |
Source | University of Michigan |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study evaluates maternal psychological distress and the impact of early palliative care team consultation on maternal anxiety and depression symptoms, coping, and quality of life/family functioning in the care of neonates born with single ventricle physiology. Half of the participants will receive early palliative care team consultation, while the other half will receive usual care (no or late palliative care intervention). The investigators hypothesize maternal stress, anxiety, and depression will be lower in the palliative care intervention group compared with the control group, and maternal coping mechanisms and perceived quality of life and family functioning will improve at the pre-discharge assessment.
Status | Completed |
Enrollment | 40 |
Est. completion date | November 15, 2016 |
Est. primary completion date | October 12, 2015 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Mothers pregnant with fetuses with single ventricle physiology who are planned to undergo staged single ventricle palliative surgery with the first surgery occurring in the neonatal period. Exclusion Criteria: - Mothers with neonates born at a gestational age of less than 32 weeks requiring admission and management in the Neonatal Intensive Care Unit. - Mothers with neonates diagnosed with major non-cardiac congenital anomalies requiring additional surgical management beyond cardiac surgery in the neonatal period. - Non-English-speaking mothers who are unable to adequately comprehend and respond to survey questions administered as part of this study. |
Country | Name | City | State |
---|---|---|---|
United States | University of Michigan C.S. Mott Children's Hospital | Ann Arbor | Michigan |
Lead Sponsor | Collaborator |
---|---|
University of Michigan |
United States,
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* Note: There are 16 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in maternal State-Trait Anxiety Index scores | Mothers will complete the State-Trait Anxiety Index to assess current anxiety symptoms and trait-like anxiety symptoms (with clinical cut-off scores defined when applicable) at a prenatal follow up visit and again prior to neonatal surgery discharge. | Up to 4 weeks | |
Primary | Change in maternal Beck Depression Index II scores | Mothers will complete the Beck Depression Index II to assess severity of depressive symptoms (with clinical cut-off scores defined when applicable) at a prenatal follow up visit and again prior to neonatal surgery discharge. | Up to 4 weeks | |
Primary | Change in maternal Brief Cope Inventory survey scores | Mothers will complete the Brief Cope Inventory to assess a broad range of coping responses (with clinical cut-off scores defined when applicable) at a prenatal follow up visit and again prior to neonatal surgery discharge. | Up to 4 weeks | |
Primary | Change in maternal PedsQL Family Impact Module survey scores | Mothers will complete the PedsQL Family Impact Module to measure the impact of the child's cardiac diagnosis on the parents and family to indicate parent functioning and overall family functioning (with clinical cut-off scores defined when applicable) at a prenatal follow up visit and again prior to neonatal surgery discharge. | Up to 4 weeks | |
Secondary | Length of neonate's intensive care unit (ICU) stay in days | Continuous days of initial ICU stay from time of admission | Participants will be followed for the duration of ICU stay, an expected average of 2 weeks | |
Secondary | Length of neonate's total hospital stay in days | Continuous acute care inpatient hospital days from day of admission until discharge | Participants will be followed for the duration of hospital stay, an expected average of 4 weeks |
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