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Postpartum DepressionNCT03415321

Development of Postnatal Mobile Support Application

A study testing Postpartum Mobile Support Application in people with Postpartum Depression and Postnatal Complication, run by Necmettin Erbakan University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

A mobile support application will be developed that will support mothers in the postpartum period and will be tested the effects of application on anxiety and depression symptoms.The study will consist of two phases. Read more about this study

Who is it for?
Ages 20 to 55 years, women onlyHealthy volunteers can take part
What is being tested?
Postpartum Mobile Support Application
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
124 participants
Where
1 siteTurkey (Türkiye)
Study dates
4 Apr 2019to 20 Feb 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 55 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Giving birth full term 39 weeks 0 days and 40 weeks 6 days (ACOG 2013)
  • Having a phone with Android feature and having an internet connection
  • Baby's normal birth weight and having APGAR score 8 and above

Who cannot join

  • Adolescent pregnants
  • Having anxiety and depression
  • Complication developments in the mother or newborn after delivery
  • Newborn stay in the intensive care unit
  • Visually impaired, hearing impaired

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Necmettin Erbakan University

    Konya, Konya

Other trials in Turkey (Türkiye)

About this study

Official title: Development of Postnatal Mobile Support Application and Evaluation of the Effectiveness of Mothers' Anxiety and Postpartum Depression Symptoms: Pre-Test Post-Test Randomized Controlled Study

A mobile support application will be developed that will support mothers in the postpartum period and will be tested the effects of application on anxiety and depression symptoms.The study will consist of two phases. The first phase of the action research (participant design method) method will be done to provide postpartum mobile support application. In the second stage, postpartum mobile support application will be evaluated for the anxiety and depression symptoms of the mothers after six weeks of use.

Read the detailed description

The postpartum period is a critical period as it is a unique milestone for many of the important physical, emotional and social changes for parents and newborns (Nilsson, Danbjorg, Larsen, Clemensen, \& Kronborg, 2015). In this period, the mother can have problems such as bleeding, infection, pain, breast problems and fatigue. In addition, adaptation to the parenting role, eventual difficulties in adaptating this role and efforts to care for the newborn can reduce the quality of life (WHO, 2012). At the beginning of the postpartum period, mothers need education and support in many subjects such as parenting, baby care, breastfeeding and relevant information and effective care (Ellberg, Hogberg, \& Lindh, 2010). The World Health Organization (WHO) also emphasizes the need in the postpartum period suggesting that breastfeeding should be supported, nutrition provided, baby development monitored and family care needs met (WHO, 2013; WHO, 1998).

In recent years, research has shown that postpartum women use information and communication technologies more and more frequently (Gibson \& Hanson, 2013) to seek health information (Walker, Im, \& Vaughan, 2012). It has been shown that tele-applications for supporting and directing parents in the postnatal period are useful in the transition to parenting in studies from Sweden and Denmark (Lindberg, Christensson, \& Öhrling, 2009; Danbjorg, Wagner, \& Clemensen, 2014b). Mobile applications providing information on pregnancy health during the prenatal period are widely used (Kennelly, Ainscough, Lindsay, Gibney, McCarthy, \& McAuliffe, 2016). It has been shown that it may be possible to meet the support needs of parents by applying innovative communication methods such as online communication at an evidence-based knowledge base. Parents saw the phone application as an informative and navigational lifestyle. Meeting new parents' information needs with chats, knowledge based and automatic messages makes them feel safe and increases their self-sufficiency (Danbjorg, Wagner, \& Clemensen, 2014a; Danbjorg, Wagner, \& Clemensen, 2014b; Danbjorg, Wagner, Kristensen, \& Clemensen , 2015). It is not possible for nurses to be at their mother's side anytime during the whole postpartum period. It is not possible to give all the necessary information without leaving the hospital and transfer the information to practice on the mother's side.

In postpartum period, care needs are increasing so that parents can adapt to their new roles and give effective care to the newborn. It is very important for the mothers to manage this period effectively for their future well-being and relations (Nilsson et. al. 2015). Studies show that mothers and fathers do not get enough postnatal care, do not feel confident with the information they have and feel insecure about what they will do.It is important for parents to feel secure in the postpartum period which in turn will have postive effects on the baby´s health and wellbeing (Danbjorg, Wagner, Kristensen, \& Clemensen, 2015; Persson, Fridlund, Kvist, \& Dykes, 2011).

Security is defined to feel safe, to be ready, to be satisfied, to feel good and to be sure (Löf et al. 2006, Forster et al 2008, Lindberg et al 2009). Insecurity is a predominant emotion for parents and is characterized by unpredictablity, uncertainity, stress, anxiety, fear, suspicion, feelings of loneliness and despair (George 2005, Forster et al 2008, Hjalmhult and Lomborg 2012). Insecurity is associated with lack of knowledge and skills experienced by parents in newborn care (George 2005, Forster et al 2008, McLachlan et al. 2009). Parents that feel they can manage the baby wellness have sense of security (Löf et al. 2006). They feel safe when they know about the needs of their newborn and aware that they, the parents, are in control of their newborns health (Persson \& Dykes 2002). Parents sense of security was associated with the strengthening behaviors they received from health professionals; unity within the family - closeness; autonomy; the mother's physical well-being and the involvement of the father during the birth and the postpartum period (Persson \& Dykes, 2002; Persson, Fridlund, \& Dykes, 2007; Persson \& Dykes, 2009; Persson, Fridlund, Kvist, \& Dykes, 2011; Persson, Fridlund, Kvist, \& Dykes, 2012).

The postpartum period is a transitional period in which mixed emotions dominate the whole family. In this period, physical symptoms, sleep deprivation, changing demands in work and home life are usually stressful and wearing. Additionally stress anxiety symptomatology has a positive relationship in susceptible people (Moran, Polanin, \& Wenzel, 2014). Anxiety usually manifests itself as extreme and persistent fear, anxiety, tension and regularly includes physical symptoms such as sleeping difficulties and lack of focus (Dennis, Falah-Hassani, Brown, \& Vigod, 2016). In studies, the anxiety prevalence rates of mothers during the first postpartum year vary between 2% and 45% (Enatescu, et al., 2014; Martini, et al., 2013). Unfortunately, there is increasing evidence that postpartum anxiety affects maternal and infant health negatively. Fatigue, loss of self-esteem and bad body sensations were seen in women who had postpartum anxiety. A deterioration in mother-infant interaction and in sleep patterns, excessive crying and also a deterioration in social relationships was shown. As anxiety acts as a trigger for development of depression, depression is often accompanied by anxiety symptoms (Dennis, Falah-Hassani, Brown, \& Vigod, 2016). Depression is a common mental disorder characterized by depressed mood, loss of interest and enjoyment, reduced energy, guilt, low self-esteem, sleep disturbances, decreased appetite and problems in focusing. Depression is a very important health problem for all ages and genders around the world.The World Health Organization (WHO) states that by 2020, depression will contribute to 5.7% of the total illness burden. Depression is the most common type of disease in women (WHO, 2010). For many women, postpartum depression (PPD) usually occurs within the first 12 weeks after birth (Dennis \& Dowswell, 2013). PPD is characterized by symptoms consistent with major depressive disorders, bipolar disorders or brief psychotic disorders occurring within 4 weeks of birth (American Psychiatric Association 2013). The symptoms associated with PPD are hopelessness, worthlessness, feelings of guilt, dissatisfaction with one's activities, difficulty in sleeping and concentration and decision-making problems (Gross \& Marcussen, 2017). Depressive symptoms in the early postpartum period vary between 5% to 20% in mothers (Patel, Baiely, Jabeen, Ali, Barker, \& Osiezagha, 2012; Kerstis, Berglund, Engström, Edlund, Sylven, \& Aarts, 2014; O'Hara \& McCabe). Dissatisfaction with marriage, antenatal life events, past depressive symptoms, late antenatal depressive symptoms, lack of social support, stressful life events and marital conflicts were identified as potential risk factors for PPD (Dennis, Brown \& Morrell, 2016). PPDnegatively affects women's quality of life, close relationships, maternal-infant interactions and infantile and school-age child development outcomes. Early diagnosis and intervention is essential to ensure optimal care for mothers, children and families when short and long term sequels of PPD are considered (McDonald, et al., 2012).

Reducing feelings of loneliness and being lonely, preventing incompatible health behaviors or reactions, increasing individual motivation, providing access to medical services or providing information about benefits, directly affects the development of PPD by supporting health and well-being positively. It is also an indirect means of prevention to identify and reduce the stress factors, increase the number of coping strategies, teaching problem-solving techniques and supporting self-sufficiency (Dennis \& Dowswell, 2013). It is clear that there must be a very good support system for all of this to be accomplished. Postpartum support for the mother is of utmost importance (Danbjorg, Wagner, Kristensen, \& Clemensen, 2015). "Current social support", including family, friends and health professionals, is one of the factors that mediate the maternal roll (Barclay, Everitt, Rogan, \& Schmied 1997; Danbjorg, Wagner, Kristensen, \& Clemensen, 2015). In theese studies, it is seen that the support systems of the mothers discharged from hospital after birth are not enough and there is no follow up. The mothers also found it difficult to access the information they need immediately (instantly). Parents were disturbed by the thought that they would disturb nurses when they were looking for help (Danbjorg, Wagner, \& Clemensen, 2014a; Danbjorg, Wagner, \& Clemensen, 2014b; Danbjorg, Wagner, Kristensen, \& Clemensen, 2015). Mothers who are postpartum, spend a lot of time caring for their newborn, but they do not have enough time to get the information they need (Guerra-Reyes, Christie, Prabhakar, Harris, \& Siek, 2016). New ways of communicating between healthcare personnel and parents are necessary. More individual timely information increases the self-confidence of mothers (Danbjorg, Wagner, \& Clemensen, 2014a; Danbjorg, Wagner, \& Clemensen, 2014b; Danbjorg, Wagner, Kristensen, \& Clemensen, 2015). In the postpartum period, adequate care and support have been reported to be associated with positive health behaviors and health outcomes, maternal stress reduction and baby health improvement (Guerra-Reyes, Christie, Prabhakar, Harris, \& Siek, 2016). There has been no study evaluating the effects of mobile support application on postpartum sense of security, anxiety and depression during the postpartum period.

Conceptual framework of the study Orem's Self-care Deficit Nursing Theory is used as the conceptual framework of this study. Acording to Orem people have a natural ability for self care and that nursing should focus on affecting that ability there is a constant need for strength and energy in order for a person to move on with his life and ability. The person has the power to self-care for her/himself and others and to determine their needs. The self-care skill required to maintain the life and function of the adult person varies from person to person. The person explores and develops different ways in describing the requirements for himself and others, and the necessary power in total. People who live together and share their responsibilities as a group are held accountable for the care of both themselves and others suffering from inadequate self-care (Orem, 2001, Fitzpatrick \& Whall, 1996). The self-care of mothers who do not receive accurate health information may be affected. Likewise, the health of the children of mothers who do not get enough information is affected.

Being tested
Postpartum Mobile Support Application
Keywords
Postpartum, Nurse, Mothers, Anxiety, Depression, Mobile Support
Medical subject headings
Depression, Postpartum, Anxiety Disorders, Depression

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Postpartum Mobile Support ApplicationDevice

    Women in the experimental group will use the Postpartum Mobile Support Application during six weeks after birth.

    Women will be evaluated three times in total, one for the first day after birth, second for the seventh day after birth and the last for the sixth week after birth.

    Short messages and calls will be remind of women's Postpartum Mobile Support Application use

Study groups in NCT03415321
Study groupRoleWhat they receive
Intervention groupExperimentalPostpartum Mobile Support Application
Receives: Device: Postpartum Mobile Support Application
Control GroupNo interventionRoutine care

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Edinburgh Postnatal Depression Scale

    Edinburgh Postnatal Depression Scale (EPDS) is a 10-item self-report scale that evaluates depressive symptoms just after delivery developed by Cox et al. (1987). EPDS will be used to assess depression in fathers and mothers. Each item is scored on a four-point scale(0-3), the minimum and maximum scores being 0 and 30,respectively. The prevalence of depression will be identified using the recommended cut-off point of 13 or above. The following severity ranges were established for the EPDS: None or minimal depression (0-6), Mild depression (7-13), Moderate depression (14-19), Severe depression (19-30).The EPDS score should not override clinical judgment. A careful clinical assessment should be carried out to confirm the diagnosis.

    Measured: Postpartum 6 weeks

Secondary outcomes (1)
  1. State-Trait Anxiety Inventory

    State-Trait Anxiety Inventory (STAI) is self-report questionnaire consists of two subscales each containing 40 items, 20 items allocated to each of the S-Anxiety and T-Anxiety subscales. It has 20 items for assessing trait anxiety and 20 for state anxiety. State anxiety items include: "I am tense; I am worried" and "I feel calm; I feel secure." Trait anxiety items include: "I worry too much over something that really doesn't matter" and "I am content; I am a steady person." All items are rated on a 4-point scale. Higher scores indicate greater anxiety. The scores obtained from the scale range theoretically from 20 to 80. Bigger score indicates high anxiety level; small score indicates low anxiety level.

    Measured: Postpartum 1th day and 6 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Jan 2018
  2. Study start4 Apr 2019
  3. Primary completion30 Jul 2019
  4. Study completion20 Feb 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Model description
A randomized controlled trial with a two-group pre-test and post-test design.
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
124 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03415321
Sponsor's protocol ID
NecmettinEU
Status last verified
Jun 2020
First submitted
8 Jan 2018
Last updated
23 Jun 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Kocak V, Ege E, Iyisoy MS. The development of the postpartum mobile support application and the effect of the application on mothers' anxiety and depression symptoms. Arch Psychiatr Nurs. 2021 Oct;35(5):441-449. doi: 10.1016/j.apnu.2021.06.009. Epub 2021 Jun 22.

    PubMed 34561057

Questions about this trial

What is this clinical trial studying?

A study testing Postpartum Mobile Support Application in people with Postpartum Depression and Postnatal Complication, run by Necmettin Erbakan University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 23 Jun 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Edinburgh Postnatal Depression Scale (time frame: Postpartum 6 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03415321, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jun 2020.

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