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OpenTrials
Completed

NCT Number: NCT02843022

Effectiveness of a Web-based Nursing Intervention in the Reduction of Postpartum Depression and Parenting Stress.

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.

Completed

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Catholic Medical Center

Manchester, New Hampshire, 03102, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Able to speak and read English
  • Access to a device which can receive text or email messages

Exclusion criteria

  • Non-English speaking,
  • No access to a device which can receive text or email messages
  • Age younger than 18 -

Treatment and study plan

standardized electronic messages

Behavioral

supportive and educational short messages

Other names: text messages, email messages

nurse phone call if requested

Behavioral

If participant responds "yes" to an offer for a phone call, a nurse calls them within a week of this response

Staff nurse phone follow-up

Behavioral

Usual care: hospital nurse or lactation consultant calls patient within 2-3 weeks prior to discharge. Message left if patient is not reached.

Primary outcomes

  1. postpartum depression symptoms

    Time frame: 6 months postpartum

    Measured by scores on the Edinburgh Postnatal Depression Scale (EPDS) at three time points

Secondary outcomes

  1. breastfeeding outcomes

    Time frame: 6 months postpartum

    Duration and pattern of infant feeding

  2. patient satisfaction/experience

    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

  3. Parenting stress

    Time frame: 6 months postpartum

    Scores on the Parenting Stress Index (PSI-4)

Sponsors and collaborators

Lead sponsor

Saint Anselm College

Other

Collaborators

  • Catholic Medical Center

Registry information

Official study title

Enhancing Follow-up Mechanisms for Women at Risk for Postpartum Depression

Important dates

Study start
2015
Primary completion
2018
Study completion
2018
First posted
Jul 25, 2016
Registry last updated
Apr 23, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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