Recruiting NCT06650683
Impact of Providing Nursing Support on Parental Stress Related to Preoperative Care of a Newborn with Hirschsprung's Disease
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Pediatric HAH.
- Who it may be relevant to
- Registry conditions: Hirschsprung Disease. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Impact of providing nursing support on parental stress related to preoperative care of a newborn with Hirschsprung's disease
Interventions
- Behavioral Pediatric HAH
Pediatric HAH nursing support for home nursery care provided by parents as part of their child's disease.
Primary outcome measures
- Questionnary to evaluate stress on parents [Time frame: From enrollment to the end of treatment at 6 months]
Secondary outcome measures (2)
- Auto-Questionnary MIB (Mother Infant Bounding) to evaluate the impact of nursing support [Time frame: From enrollment to the end of treatment at 6 months]
- Self-Questionnary Burden inventory to evaluate the nursery training provided [Time frame: From enrollment to the end of treatment at 6 months]
Eligibility criteria
Inclusion criteria
- Families (one or two parents) with a newborn or infant under 2 months with confirmed or suspected Hirschsprung disease, for whom nursings are effective and performed 1 to 2 times a day while waiting for surgery.
- With a possible return home before surgery
- With an information leaflet and non-opposition form signed by one or both parent(s) or by the legal representative.
Exclusion criteria
- The absence of daily nursings
- Initial ineffectiveness of nursings requiring a digestive stoma
- Failure to return home before surgery
- Refusal of one or both parent(s) or legal representative(s)
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Non-randomized
- Model
- Sequential
- Masking
- Single blind
- Primary purpose
- Supportive care
Study locations
France · 1 center
- APHM — Marseille
Identifiers
NCT: NCT06650683 · RCAPHM22_0037 · 2022-A02696-37