Effect of parental participation on bedside clinical rounds for their child in NICU compared to non-participation on parental satisfaction and level of parental stress.

A/Prof Abdel-Latif Mohamed0 个研究点目标入组 110 人开始时间: 2012年5月10日最近更新: 2020年1月13日

适应症

试验速览

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•Parents (mother and/or their partners) or guardians who fulfil the following criteria will be approached for inclusion in the study:
•If their infant is anticipated to stay in NICU for minimal of 11 days. This cut-off is taken as the intervention (PPCBR and non-PPCBR) and washout period will take minimum of 3 days each. In addition we allowed first 2 days for not being included in the study as most mothers will be recovering from delivery/Caesarean Section/Anaesthesia …etc).

•Parents (mother and/or their partners) or guardians who fulfil the following criteria will be excluded from the study:
•1. If their infant is anticipated to stay in NICU for less than 11 days
•2. If their infant is anticipated to be transferred to another NICU or local hospital in less than 11 days after admission.
•3. Refused to participate in the study
•4. Parents or guardians who do not have good command of English (it is not practical to include an interpreter during the rounds as this might put pressure on interpreter service (eg. to attend rounds at 08:30 daily for 7 days per patient and also it will lead to significant delay in the rounds).

发起方

A/Prof Abdel-Latif Mohamed