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
NA
100 participants
INTERVENTIONAL
2019-02-01
2019-12-12
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SCREENING
NONE
Study Groups
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Anxiety and depression screening
Hospital Anxiety and Depression Scale (HADS) questionnaire administered at the start of the study. After two weeks or at the time of discharge, participants will complete the HADS questionnaire again
Anxiety and depression screening
At the time of consent, the participant parent will be randomized into either the control or intervention groups. The control group will complete the Hospital Anxiety and Depression Scale (HADS) questionnaire at the start of the study. After two weeks or at the time of discharge, the control group will complete the HADS questionnaire again.
Journaling
Parents randomized into the intervention group be given verbal instructions to use a journal how/when they choose for the duration of the intervention period
Anxiety and depression screening with journaling
Parents randomized into the intervention group be given verbal instructions to use a journal how/when they choose for the duration of the intervention period. They will also complete the HADS questionnaire before and after the intervention period of two weeks. At the end of the intervention period, these parents will also complete a survey regarding their experience with journaling
Journaling
Parents randomized into the intervention group be given verbal instructions to use a journal how/when they choose for the duration of the intervention period
Interventions
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Anxiety and depression screening
At the time of consent, the participant parent will be randomized into either the control or intervention groups. The control group will complete the Hospital Anxiety and Depression Scale (HADS) questionnaire at the start of the study. After two weeks or at the time of discharge, the control group will complete the HADS questionnaire again.
Journaling
Parents randomized into the intervention group be given verbal instructions to use a journal how/when they choose for the duration of the intervention period
Eligibility Criteria
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Inclusion Criteria
* \> 28 weeks gestation
* At least 5 days anticipated admission in Vanderbilt NICU
Exclusion Criteria
* Expected death or discharge within 5 days of admission
* Primary medical team feels that participation would be disruptive or detrimental to infant's care
ALL
Yes
Sponsors
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Vanderbilt University Medical Center
OTHER
Responsible Party
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Laura Shashy
Clinical Fellow
Principal Investigators
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Amy Weitlauf, PHD
Role: STUDY_CHAIR
Vanderbilt University Medical Center
Locations
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Vanderbilt University Medical Center
Nashville, Tennessee, United States
Countries
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References
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Russell LN, Gregory ML, Warren ZE, Weitlauf AS. Uptake and impact of journaling program on wellbeing of NICU parents. J Perinatol. 2021 Aug;41(8):2057-2062. doi: 10.1038/s41372-021-00983-1. Epub 2021 Mar 1.
Other Identifiers
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181831
Identifier Type: -
Identifier Source: org_study_id
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