Parental presence on bedside clinical rounds (PPBCR) in a neonatal intensive care unit (NICU).
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 Mohamed
110 participants
Apr 15, 2012
Interventional
Conditions
Summary
Why are we doing this study? * ACT Health and The Canberra Hospital are motivated to provide care that is both family and patient centred. Currently in the Centre for Newborn Care parents are not involved in clinical bedside rounds. This study will allow parents to attend these rounds for a specified period and gain feedback from the experience via surveys. * We aim to use the information gained from this study to introduce a new way of doing clinical beside rounds in our soon to be completed Womens’ and Childrens’ Hospital. What does the study involve? * After obtaining consent, the participant (parents or guardian) will be randomised to one of two arms: 1. PPBCR group (attending bedside clinical rounds with health care professionals) or 2. Non-PPCBR (non-attending bedside clinical rounds with health care professionals). * Each group depending on the baby’s gestation will rotate between attending and not attending rounds spending 3 (if the infant gestation is more than 30 weeks) or 7 (if the infant gestation is less than or equal 30 weeks) days in each group with a similar break in between. * The participant will be given regular updates on their baby condition during non-PPCBR and washout break * At conclusion of each arm, the participant will be asked to complete: 1. NICU parental stressor scale and 2. A satisfaction survey about being involved in clinical bedside rounds What do we hope to achieve with this study? Through your involvement in this study we aim to: * Improve communication between families and the clinical team within the Centre for Newborn Care. * Families being more aware of current clinical management and care plan for their babies, in turn reducing stressors they may experience.
Eligibility
Plain Language Summary
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Interventions
* The intervention involves the participant (parents or guardian) accompany health care professionals on their bedside clinical rounds to their child. * After obtaining consent, the participant will be randomised to one of two arms: 1. Attending bedside clinical rounds with health care professionals (PPBCR) group or 2. Non-attending bedside clinical rounds with health care professionals (Non-PPCBR) group. * Parents will rotate between the above two arms but they will have a break (washout period) before changing from one group to the other. * The duration of time spent in each group and in washout period depends on their infant gestation. If the infant gestation is more than 30 weeks then duration will be 3 days in each group and washout period (that’s total of 9 days in the whole study). If the infant gestation is less than or equal 30 weeks then duration will be 7 days in each group and washout period (that’s total of 21 days in the whole study). * At conclusion of each arm, the participant will be asked to complete: 1. NICU parental stressor scale and 2. A satisfaction survey about being involved in clinical bedside rounds.
Locations(1)
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ACTRN12612000506897