Feasibility, acceptability and experiences of intrapartum fetal monitoring by caregivers using the Moyo device at Mbale regional referral hospital:

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dc.contributor.author Nakawuki, Ashley Winfred
dc.date.accessioned 2026-03-09T12:36:51Z
dc.date.available 2026-03-09T12:36:51Z
dc.date.issued 2025-11
dc.identifier.citation Nakawuki, A.W. (2025). Feasibility, acceptability and experiences of intrapartum fetal monitoring by caregivers using the Moyo device at Mbale regional referral hospital: A pilot quasi experimental study. Busitema University. Unpublished dissertation. en_US
dc.identifier.uri http://hdl.handle.net/20.500.12283/4692
dc.description Dissertation en_US
dc.description.abstract Background: Intrapartum fetal heart rate monitoring (FHRM) is essential for identifying fetal distress and preventing asphyxia-related complications. However, inadequate FHRM due to staffing shortages is a critical issue in low-resource settings such as Uganda, where intrapartumrelated neonatal deaths are high. The Moyo device, a portable fetal heart rate (FHR) monitor, reduced perinatal morbidity and mortality in a recently conducted trial in Mbale. However, its potential remains underutilized due to a high patient-to-midwife ratio. Recent evidence suggests that task-sharing FHRM with caregivers may address poor fetal monitoring practices, enabling non-clinical individuals to support the timely identification of fetal distress. Objective: This study assessed the feasibility, acceptability, and caregivers' experiences with intrapartum FHRM using the Moyo device at Mbale Regional Referral Hospital (MRRH), Eastern Uganda. Methods: A pilot quasi-experimental study design was used employing a sequential explanatory mixed-methods approach at MRRH. Caregivers of labouring women were consecutively enrolled, trained, and guided to monitor FHR every 30 minutes using the Moyo device. Feasibility was defined as achieving a mean monitoring interval within 30 ± 5 minutes, while acceptability was assessed using a five-point Likert scale converted into percentage scores and categorized using Bloom’s criteria. Experiences of caregivers who used the Moyo were explored through structured, in-depth interviews. Quantitative data were analysed using Stata version 17, and qualitative data were analysed thematically using Atlas. ti. Results: A total of 75 caregivers participated, with a median age of 32 years (IQR: 25–42). Most were female (n=70, 93.3%) and had primary-level education (n=35, 46.7%). The majority of participants (n=74, 98.7%) were able to use the Moyo device to check and document FHR, with 65 (86.7%) reporting no technical issues. However, only 34.7% (n=26) of caregivers were able to monitor FHR at 30-minute intervals, and 65.3% (n=49) of readings within 60 minutes. The median number of FHR recordings was 3 (IQR: 1–10), and the mean duration of the active stage of labour was 10.9 ± 9.7 hours. Feasibility was higher among caretakers who were first or second-degree relatives (61.5%; p = 0.037). The majority of the caregivers (n=70, 93.3%) found FHRM using the Moyo device acceptable. Caregivers reported positive experiences with the Moyo device, driven by curiosity, reassurance about fetal safety, and a desire to learn. Conclusion: Intrapartum FHRM by caregivers using the Moyo device was highly acceptable, and most caregivers correctly used the device. However, adherence to the recommended 30-minute monitoring interval remained low. Similar initiatives involving caregivers should prioritize practical support systems like reminders and workflow integration to enable timely recordings and improve adherence to recommended FHR monitoring. en_US
dc.description.sponsorship Assoc. Professor Mukunya David : Assoc. Professor Milton Musaba en_US
dc.language.iso en en_US
dc.publisher Busitema University en_US
dc.subject Intrapartum monitoring en_US
dc.subject Fetal heart rate en_US
dc.subject Moyo device en_US
dc.subject Task sharing en_US
dc.subject Caregiver en_US
dc.title Feasibility, acceptability and experiences of intrapartum fetal monitoring by caregivers using the Moyo device at Mbale regional referral hospital: en_US
dc.title.alternative A pilot quasi experimental study en_US
dc.type Other en_US


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