A group intervention for pregnant multiparas with fear of childbirth: A protocol of a feasibility study of the MOTIVE trial

•The MOTIVE intervention was designed for multiparas with fear of childbirth.•This is a protocol for a feasibility study with a mixed-methods design.•The findings will provide insights on the feasibility and acceptability of MOTIVE.•The results will inform revisions to the intervention.•Based on the...

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Veröffentlicht in:Sexual & reproductive healthcare 2024-09, Vol.41, p.101003, Article 101003
Hauptverfasser: Sandström, Laura, Kaunonen, Marja, Aho, Anna Liisa
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Sprache:eng
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Zusammenfassung:•The MOTIVE intervention was designed for multiparas with fear of childbirth.•This is a protocol for a feasibility study with a mixed-methods design.•The findings will provide insights on the feasibility and acceptability of MOTIVE.•The results will inform revisions to the intervention.•Based on the results a larger-scale trial evaluation can be done. 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. 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. 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.
ISSN:1877-5756
1877-5764
1877-5764
DOI:10.1016/j.srhc.2024.101003