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      Living with Loss: study protocol for a randomized controlled trial evaluating an internet-based perinatal bereavement program for parents following stillbirth and neonatal death

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          Abstract

          Background

          Stillbirth and neonatal death are devastating pregnancy outcomes with long-lasting psychosocial consequences for parents and families, and wide-ranging economic impacts on health systems and society. It is essential that parents and families have access to appropriate support, yet services are often limited. Internet-based programs may provide another option of psychosocial support for parents following the death of a baby. We aim to evaluate the efficacy and acceptability of a self-guided internet-based perinatal bereavement support program “Living with Loss” (LWL) in reducing psychological distress and improving the wellbeing of parents following stillbirth or neonatal death.

          Methods

          This trial is a two-arm parallel group randomized controlled trial comparing the intervention arm (LWL) with a care as usual control arm (CAU). We anticipate recruiting 150 women and men across Australia who have experienced a stillbirth or neonatal death in the past 2 years. Participants randomized to the LWL group will receive the six-module internet-based program over 8 weeks including automated email notifications and reminders. Baseline, post-intervention, and 3-month follow-up assessments will be conducted to assess primary and secondary outcomes for both arms. The primary outcome will be the change in Kessler Psychological Distress Scale (K10) scores from baseline to 3-month follow-up. Secondary outcomes include perinatal grief, anxiety, depression, quality of life, program satisfaction and acceptability, and cost-effectiveness. Analysis will use intention-to-treat linear mixed models to examine psychological distress symptom scores at 3-month follow-up. Subgroup analyses by severity of symptoms at baseline will be undertaken.

          Discussion

          The LWL program aims to provide an evidence-based accessible and flexible support option for bereaved parents following stillbirth or neonatal death. This may be particularly useful for parents and healthcare professionals residing in rural regions where services and supports are limited. This RCT seeks to provide evidence of the efficacy, acceptability, and cost-effectiveness of the LWL program and contribute to our understanding of the role digital services may play in addressing the gap in the availability of specific bereavement support resources for parents following the death of a baby, particularly for men.

          Trial registration

          Australian New Zealand Clinical Trials Registry, ACTRN12621000631808. Registered prospectively on 27 May 2021.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s13063-022-06363-0.

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          Most cited references64

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          A brief measure for assessing generalized anxiety disorder: the GAD-7.

          Generalized anxiety disorder (GAD) is one of the most common mental disorders; however, there is no brief clinical measure for assessing GAD. The objective of this study was to develop a brief self-report scale to identify probable cases of GAD and evaluate its reliability and validity. A criterion-standard study was performed in 15 primary care clinics in the United States from November 2004 through June 2005. Of a total of 2740 adult patients completing a study questionnaire, 965 patients had a telephone interview with a mental health professional within 1 week. For criterion and construct validity, GAD self-report scale diagnoses were compared with independent diagnoses made by mental health professionals; functional status measures; disability days; and health care use. A 7-item anxiety scale (GAD-7) had good reliability, as well as criterion, construct, factorial, and procedural validity. A cut point was identified that optimized sensitivity (89%) and specificity (82%). Increasing scores on the scale were strongly associated with multiple domains of functional impairment (all 6 Medical Outcomes Study Short-Form General Health Survey scales and disability days). Although GAD and depression symptoms frequently co-occurred, factor analysis confirmed them as distinct dimensions. Moreover, GAD and depression symptoms had differing but independent effects on functional impairment and disability. There was good agreement between self-report and interviewer-administered versions of the scale. The GAD-7 is a valid and efficient tool for screening for GAD and assessing its severity in clinical practice and research.
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            SPIRIT 2013 statement: defining standard protocol items for clinical trials.

            The protocol of a clinical trial serves as the foundation for study planning, conduct, reporting, and appraisal. However, trial protocols and existing protocol guidelines vary greatly in content and quality. This article describes the systematic development and scope of SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) 2013, a guideline for the minimum content of a clinical trial protocol.The 33-item SPIRIT checklist applies to protocols for all clinical trials and focuses on content rather than format. The checklist recommends a full description of what is planned; it does not prescribe how to design or conduct a trial. By providing guidance for key content, the SPIRIT recommendations aim to facilitate the drafting of high-quality protocols. Adherence to SPIRIT would also enhance the transparency and completeness of trial protocols for the benefit of investigators, trial participants, patients, sponsors, funders, research ethics committees or institutional review boards, peer reviewers, journals, trial registries, policymakers, regulators, and other key stakeholders.
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              Detection of postnatal depression. Development of the 10-item Edinburgh Postnatal Depression Scale.

              The development of a 10-item self-report scale (EPDS) to screen for Postnatal Depression in the community is described. After extensive pilot interviews a validation study was carried out on 84 mothers using the Research Diagnostic Criteria for depressive illness obtained from Goldberg's Standardised Psychiatric Interview. The EPDS was found to have satisfactory sensitivity and specificity, and was also sensitive to change in the severity of depression over time. The scale can be completed in about 5 minutes and has a simple method of scoring. The use of the EPDS in the secondary prevention of Postnatal Depression is discussed.
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                Author and article information

                Contributors
                siobhan.loughnan@mater.uq.edu.au
                f.boyle@uq.edu.au
                d.ellwood@griffith.edu.au
                sara.crocker@mater.uq.edu.au
                ann.lancaster@mater.uq.edu.au
                j.dean2@uq.edu.au
                d.horey@latrobe.edu.au
                emily.callander@monash.edu.au
                c.jackson@uq.edu.au
                antonia.shand@health.nsw.gov.au
                vicki.flenady@mater.uq.edu.au
                Journal
                Trials
                Trials
                Trials
                BioMed Central (London )
                1745-6215
                6 June 2022
                6 June 2022
                2022
                : 23
                : 464
                Affiliations
                [1 ]GRID grid.1003.2, ISNI 0000 0000 9320 7537, NHMRC Centre of Research Excellence in Stillbirth, , Mater Research Institute-University of Queensland, ; Raymond Terrace, Level 3 Aubigny Place, South Brisbane, QLD Australia
                [2 ]GRID grid.1003.2, ISNI 0000 0000 9320 7537, Institute for Social Science Research, The University of Queensland, ; 80 Meiers Rd, Indooroopilly, QLD Australia
                [3 ]GRID grid.1022.1, ISNI 0000 0004 0437 5432, School of Medicine, , Griffith University, ; Parklands Drive, Gold Coast, QLD Australia
                [4 ]GRID grid.413154.6, ISNI 0000 0004 0625 9072, Gold Coast University Hospital, ; 1 Hospital Drive, Southport, QLD Australia
                [5 ]GRID grid.1018.8, ISNI 0000 0001 2342 0938, La Trobe University, ; Plenty Rd &, Kingsbury Dr, Bundoora, VIC Australia
                [6 ]GRID grid.1002.3, ISNI 0000 0004 1936 7857, Monash University, ; 553 St Kilda Road, Melbourne, VIC Australia
                [7 ]GRID grid.1003.2, ISNI 0000 0000 9320 7537, The University of Queensland, ; St Lucia, QLD Australia
                [8 ]GRID grid.1013.3, ISNI 0000 0004 1936 834X, Faculty of Medicine and Health, , The University of Sydney, ; Camperdown, NSW Australia
                Author information
                http://orcid.org/0000-0002-8763-2822
                Article
                6363
                10.1186/s13063-022-06363-0
                9167910
                57a5e7ff-6f78-427d-a8fa-281d3664cb1a
                © The Author(s) 2022

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 24 February 2022
                : 26 April 2022
                Funding
                Funded by: Australian Government's Medical Research Future Fund (MRFF) Rapid Applied Research Translation program
                Award ID: Awarded to Brisbane Diamantina Health Partners (now known as Health Translation Queensland)
                Award Recipient :
                Categories
                Study Protocol
                Custom metadata
                © The Author(s) 2022

                Medicine
                stillbirth,neonatal death,pregnancy loss,perinatal,internet,online,bereavement,grief,distress,anxiety
                Medicine
                stillbirth, neonatal death, pregnancy loss, perinatal, internet, online, bereavement, grief, distress, anxiety

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