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Clinical Trials/ACTRN12612000506897
ACTRN12612000506897
Recruiting
未知

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 sites110 target enrollmentMay 10, 2012

Overview

Phase
未知
Intervention
Not specified
Conditions
Parental presence on bedside clinical rounds in NICU
Sponsor
A/Prof Abdel-Latif Mohamed
Enrollment
110
Status
Recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 10, 2012
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
A/Prof Abdel-Latif Mohamed

Eligibility Criteria

Inclusion Criteria

  • 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).

Exclusion Criteria

  • 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).

Outcomes

Primary Outcomes

Not specified

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