Global Survey on Newborns' HOspitalisation and Parental Experiences - the HOPE Study

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorGlobal Foundation for the Care of Newborn Infants

About this trial

This study aims to explore parents' experiences and emotional burdens related to their newborn's hospital stay using an online survey. Our target population consists of parents of newborns born preterm, with low birthweight, or critically ill. Particularly the presence of infant- and family-centred developmental care (IFCDC) principles as well as support through political framework conditions will be investigated.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

Other family members than parents/(primary) caregivers

Parents of newborns that did not receive special/intensive care starting within the first week of life

Parents or caregivers of infants born before 1 January 2023

Persons with insufficient proficiency of one of the languages of the questionnaire

Trial population

Parent or caregiver of a newborn infant born on January 1, 2023, or thereafter, who received/is receiving special/intensive care starting within the first week of life such as oxygen therapy or other respiratory support, incubator treatment, intravenous infusions, treatment of (suspected) sepsis, pneumonia, necrotising enterocolitis, malformations, jaundice, nutritional/feeding problems, hypoglycemia, etc.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • N/A, no intervention, participation in survey

    Other intervention

    N/A, no intervention, participation in survey

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: Parents/participants1 intervention

Trial outcomes

Primary outcomes

1

Infant Family-Centered Developmental Care principles

The implementation of IFCDC principles will be measured as the percentage of infants receiving specific care, such as skin-to-skin contact, receiving breastfeeding support, access of parents/caregivers to the neonate, involvement in daily care procedures etc.

Time frame
01/09/2025 - 31/12/2027

Secondary outcomes

1

Social/Financial/Political Support (Quantitative)

This section will include approximately 10 questions assessing quantitative data on support received by the mother/parents, such as support to access of care, financial compensation for additional expenses (transportation to the hospital, reimbursement for sleeping facilities), social/political support, such as maternity leave etc. The final outcome still depends on the expert decision.

Time frame
01/09/2025 - 31/12/2027
2

Social/Financial/Political Support (Qualitative)

Subjective qualitative data on support received by the mother/parents, such as support to access of care, financial compensation for additional expenses, social/political support, such as maternity leave etc. indicated by participants via open text fields.

Time frame
01/09/2025 - 31/12/2027
3

Participant characteristics

Data on Participant characteristics will be collected (such as marital status, parental education etc., and infant characteristics to analyse the influence of these data on the availability of care according the IFCDC principles and describe the study sample.

Time frame
01/09/2025 - 31/12/2027
4

Questionnaire pre-testing (quantitative)

Quantitative evaluation data of the pre-testing of the questionnaire related to the understandability of questions, utilisation of lay language, appropriateness of selected questions.

Time frame
01/09/2025 - 31/12/2027

Other outcomes

1

Single-Country evaluation of IFCDC implementation

The level IFCDC implementation will be analysed per country. Inter-country comparison will be performed to derive recommendations for action.

Time frame
01/09/2025 - 31/12/2027
2

Single-Country evaluation on the availability of supportive political measures

The availability of supportive political measures will be analysed per country. Inter-country comparison will be performed to derive recommendations for action.

Time frame
01/09/2025 - 31/12/2027

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: