Family Integrated Care in the NICU (FICare)
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| ClinicalTrials.gov Identifier: NCT01852695 |
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Recruitment Status : Unknown
Verified October 2015 by Mount Sinai Hospital, Canada.
Recruitment status was: Active, not recruiting
First Posted : May 14, 2013
Last Update Posted : October 4, 2016
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In the highly technological environment of the modern neonatal intensive care unit (NICU), the infant is physically, psychologically and emotionally separated from its parents. Recognition that this impedes parent- infant interaction and is detrimental to the infant, led to the development of programs such as family centered care, kangaroo care and skin-to-skin care1-3. However, they are based on the common premise that only NICU professionals with special skills can provide care for the infant. Parents are relegated to a supportive role, and some have described themselves as voyeurs who are "allowed" to visit and hold their infants4. Many feel anxious and unprepared to care for their infants after discharge5.
In 1979, a shortage of NICU nurses in Estonia prompted Levin1,6 to implement a "humane" care model in which parents provided nursing care for the infant (except for administration of IV fluid and medication), while nurses provided teaching and guidance to parents. This resulted in 30% improvement in weight gain1,30% reduction in infections, 20% reduction in NICU length of stay, 50% reduction in nurse utilization and overall improved satisfaction among parents and staff [personal communication, Levin,A.]. Building on the Estonian experience, we have developed a new Family Integrated Care (FIC) model that is adapted for the NICU environment in North America. In a pilot study at Mount Sinai Hospital, Toronto 46 infants and their families were enrolled in the study. Preliminary results and feedback from parents and healthcare providers (HCP) show that the FIC model is both feasible and safe, and may lead to improved outcomes including improved weight gain(paper submitted for publication). This study is a cluster randomized controlled trial in 16 tertiary level NICUs, to evaluate the efficacy of the FIC model in Canada.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Premature Birth | Behavioral: Family Integrated Care | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 720 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Official Title: | A Family Integrated Care Model For The Neonatal Intensive Care Unit: A Cluster Randomised Controlled Trial |
| Study Start Date : | March 2013 |
| Actual Primary Completion Date : | October 2015 |
| Estimated Study Completion Date : | March 2017 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Family Integrated Care Arm
Parents are integrated into the care of their infants in the NICU. Parents consent to spending up to eight hours a day with their infant, attend special education sessions, participate in daily medical rounds, and do basic infant charting. This will enable parents to provide care for infants with nursing supervision in the areas of feeding, bathing, dressing and holding skin to skin.
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Behavioral: Family Integrated Care
Parents are integrated into the care of their infants in the NICU. Parents consent to spending up to eight hours a day with their infant, attend special education sessions, participate in daily medical rounds, and do basic infant charting. This will enable parents to provide care for infants with nursing supervision in the areas of feeding, bathing, dressing and holding skin to skin. |
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No Intervention: Control Arm
Regular care by nurse will be provided to patients admitted to control sites.
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- Weight Gain [ Time Frame: Day 0-21 ]Change in weight from enrollment to day 21 following commencement of the intervention
- Weight gain velocity [ Time Frame: Day 0-21 ]Weight gain velocity at 21 days post-intervention commencement;
- Breastfeeding rate [ Time Frame: up to 16 weeks ]Participants will be followed until first discharge home from hospital, an expected average 13 weeks
- Clinical outcomes (mortality and Nosocomial infection (NI), Necrotizing Enterocolitis (NEC), Bronchopulmonary Dysplasia(BPD), Retinopathy of prematurity(ROP) & Intraventricular haemorrhage(IVH) [ Time Frame: up to 16 weeks ]Patients will be followed for the duration of their hospital stay for an expected average of 13 weeks. Mortality and five major morbidities: (a) Nosocomial infection will be defined using the Center for Disease Control criteria; (b) Necrotizing enterocolitis is defined using Bell's criteria;(c) Bronchopulmonary dysplasia is defined according to Shennan et al; (d) Intraventricular hemorrhage will be classified using the Canadian Pediatric Society classification, from cranial ultrasound performed during the first 28 days of life; (e) Retinopathy of prematurity will be staged according to the International Classification of Retinopathy of Prematurity.
- Safety [ Time Frame: 1000 patient days ]Number of critical incident reports/1000 patient days
- Parental stress and anxiety [ Time Frame: Day 0 and when the infant reaches 35 weeks corrected gestational age ]We will administer questionnaires to parents in the first week following admission and when their infant reaches 35 weeks corrected gestational age, in both the intervention and control sites
- Resource Use [ Time Frame: Day 0 -week 16 ]Data on health care utilisation will be collected during the patients entire hospital stay until the first discharge home, averaging 13 weeks including length of stay, duration of oxygen therapy. Per diem costs will be used to estimate potential cost savings derived from any reduced length of stay.
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| Ages Eligible for Study: | up to 33 Weeks (Child) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- < 33 weeks gestational age at birth;
- On no respiratory support or low level respiratory support (i.e., oxygen by cannula or mask, or continuous positive airway pressure (CPAP);
- A primary caregiver parent who is willing and able to commit to spending at least 8 hours per day with her/his infant between the hours of 0700 and 2000;
- Parental consent.
Exclusion Criteria:
- Palliative care;
- Major life threatening congenital anomaly;
- Critical illness (unlikely to survive);
- On high level of respiratory support (mechanical ventilator, high frequency oscillatory or jet ventilation, extra-corporeal membrane oxygenation)
- Parental request for early transfer to another hospital;
- Parental inability to participate (e.g., health, social or language issues that might inhibit their ability to communicate with the healthcare team).
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01852695
| Canada, Alberta | |
| Foothills Medical Centre | |
| Calgary, Alberta, Canada | |
| Canada, Manitoba | |
| Health Sciences Centre, Winnipeg | |
| Winnipeg, Manitoba, Canada | |
| St. Boniface General Hospital | |
| Winnipeg, Manitoba, Canada | |
| Canada, New Brunswick | |
| The Moncton Hospital | |
| Moncton, New Brunswick, Canada | |
| Saint John Regional Hospital | |
| Saint John, New Brunswick, Canada | |
| Canada, Nova Scotia | |
| IWK Health Centre | |
| Halifax, Nova Scotia, Canada | |
| Canada, Ontario | |
| Hamilton Health Sciences Centre | |
| Hamilton, Ontario, Canada | |
| London Health Sciences Centre | |
| London, Ontario, Canada | |
| Hospital for Sick Children | |
| Toronto, Ontario, Canada | |
| Sunnybrook Health Sciences Centre | |
| Toronto, Ontario, Canada | |
| Windsor Regional Hospital | |
| Windsor, Ontario, Canada | |
| Canada, Quebec | |
| Centre hospitalier universitaire de Québec | |
| Laval, Quebec, Canada | |
| Centre Hospitalier Universitaire de Sherbrooke | |
| Sherbrooke, Quebec, Canada | |
| Canada, Saskatchewan | |
| Regina General Hospital | |
| Regina, Saskatchewan, Canada | |
| Royal University Hospital | |
| Saskatoon, Saskatchewan, Canada | |
| Principal Investigator: | Shoo K Lee, FRCPC PhD | MOUNT SINAI HOSPITAL |
| Responsible Party: | Mount Sinai Hospital, Canada |
| ClinicalTrials.gov Identifier: | NCT01852695 |
| Other Study ID Numbers: |
122173 |
| First Posted: | May 14, 2013 Key Record Dates |
| Last Update Posted: | October 4, 2016 |
| Last Verified: | October 2015 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
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Family integrated Care Family centered care NICU family centered care NICU parent program |
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Premature Birth Obstetric Labor, Premature Obstetric Labor Complications |
Pregnancy Complications Female Urogenital Diseases and Pregnancy Complications Urogenital Diseases |