Catholic Medical Center
Manchester, New Hampshire, 03102, United States
NCT Number: NCT02843022
The purpose of the study is to determine whether a web-based nursing intervention delivered during the postpartum period will decrease symptoms of postpartum depression and parenting stress.
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Notify Me18 year and older
Female
Interventional
Not applicable
Manchester, New Hampshire, 03102, United States
The purpose of this randomized, controlled trial is to determine whether receiving standardized messages (text or email) from a postpartum nurse four times/week for 6 months after delivery will decrease symptoms of postpartum depression and parenting stress. Enrolled women will be randomized to one of three groups. The first group will receive the usual care, which is a phone call from a nurse within the first few weeks postpartum. The second group will receive four standardized messages each week, the content of which will include infant care, maternal self-care and inspirational material. The third group will receive the same four standardized messages each week, and in addition, two of these weekly messages will offer the option to respond with a request for a nurse to call them. Baseline data will be collected during the postpartum hospitalization, and follow-up will occur by email at 3 weeks, 3 months and 6 months postpartum.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
supportive and educational short messages
Other names: text messages, email messages
If participant responds "yes" to an offer for a phone call, a nurse calls them within a week of this response
Usual care: hospital nurse or lactation consultant calls patient within 2-3 weeks prior to discharge. Message left if patient is not reached.
Time frame: 6 months postpartum
Measured by scores on the Edinburgh Postnatal Depression Scale (EPDS) at three time points
Time frame: 6 months postpartum
Duration and pattern of infant feeding
Time frame: 6 months postpartum
Participant response to the experience of receiving messages and having the option to talk to a nurse (group 3), as well as their sense of connection to the hospital where they gave birth
Time frame: 6 months postpartum
Scores on the Parenting Stress Index (PSI-4)
Saint Anselm College
Other
Enhancing Follow-up Mechanisms for Women at Risk for Postpartum Depression
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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