对有分娩恐惧的多胎妊娠妇女进行集体干预:MOTIVE 试验可行性研究方案。

IF 1.4 3区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Sexual & Reproductive Healthcare Pub Date : 2024-07-01 DOI:10.1016/j.srhc.2024.101003
Laura Sandström , Marja Kaunonen , Anna Liisa Aho
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引用次数: 0

摘要

背景:尽管对分娩恐惧的研究兴趣日益浓厚,但针对有分娩恐惧的多胎妊娠妇女的干预措施却一直被忽视,尽管未经治疗的分娩恐惧会对母亲和整个家庭造成严重的不良影响。因此,我们设计了 MOTIVE(通过干预和赋权克服分娩恐惧的多胎妊娠),这是一项针对有分娩恐惧的多胎妊娠的干预措施:本文是 MOTIVE 试验的单臂非随机可行性研究方案,采用混合方法设计。干预的主要目的是帮助有分娩恐惧的多胎妊娠妇女,以达到减轻恐惧的预期效果。MOTIVE 包括四次小组会议(每次 2 小时);三次在孕期,一次在产后,另外还有一次产后电话会议。干预措施由一名助产士和一名产科医院的精神科护士提供。定量数据将通过基线、基线后 4 周和干预后三个时间点的自我报告问卷收集。定性数据将通过日记、干预后问卷中的开放式问题和个别访谈收集。目标是在 12 个月的时间内,将四名多胎妊娠者分成四组:讨论:研究结果将有助于深入了解干预措施的可行性和可接受性,并为干预措施的修订提供依据。讨论:研究结果将有助于深入了解干预措施的可行性和可接受性,并为干预措施的修订提供依据。研究结果将为制定明确的、更大规模的试验评估提供指导,以进一步检验改进后的干预措施的有效性。
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A group intervention for pregnant multiparas with fear of childbirth: A protocol of a feasibility study of the MOTIVE trial

Background

Although research interest in fear of childbirth has increased, interventions targeting especially multiparas with fear of childbirth have been overlooked, although untreated fear can cause serious adverse effects on the mother and the whole family. Thus MOTIVE (Multiparas overcoming Childbirth Fear Through Intervention and Empowerment), an intervention for pregnant multiparas with fear of childbirth, was designed.

Methods

This is a protocol of a single-arm non-randomized feasibility study of the MOTIVE trial with a mixed-methods design. The primary aim of the intervention is to assist pregnant multiparas with fear of childbirth, with the desired outcome to alleviate fear. MOTIVE consists of four group sessions (2 h each); three during pregnancy and one after giving birth and in addition of a phone call after birth. The intervention is provided by a midwife and a psychiatric nurse at the maternity hospital. Quantitative data will be gathered via self-report questionnaires at three time points, at baseline, at 4 weeks post-baseline and post-intervention. Qualitative data will be gathered by diaries, open-ended questions from post-intervention questionnaires, and individual interviews. The target is to assemble four groups of four multiparas over a 12-month period.

Discussion

The findings will provide insights into the feasibility and acceptability of the intervention and will inform revisions to it. The results will guide the development of a definitive, larger-scale trial evaluation to further examine the efficacy of the refined intervention.

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来源期刊
Sexual & Reproductive Healthcare
Sexual & Reproductive Healthcare PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
2.70
自引率
5.60%
发文量
73
审稿时长
45 days
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