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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06414200
Other study ID # NL84484.078.23
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date December 1, 2024
Est. completion date March 31, 2027

Study information

Verified date May 2024
Source Erasmus Medical Center
Contact Esther J van Steenbergen, Msc
Phone +31107030380
Email e.vansteenbergen@erasmusmc.nl
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this stepped wedge cluster randomized trial is to compare nutritional care after discharge to an intervention in children term born - 18 years old discharged with newly initiated nutritional care. The main question it aims to answer is: To investigate whether a tailored nutritional care follow-up program in children who are being discharged from the hospital with nutritional support improves nutritional intake and status as well as feeding behavior and quality of life (QoL) in children and their parents. Furthermore, the effect on parental stress, anxiety, depression, and post-traumatic stress (PTSD) as well as QoL will be assessed with and without a tailored nutritional care follow-up program


Description:

All subjects, both in the usual care and intervention group, will be treated with the standard nutritional protocols of these individual hospitals during hospitalization. After hospital discharge, the treatments of the intervention and the control group will entail the procedures as described below. Intervention group The intervention consists of a tailored nutritional follow-up plan, including a parent empowerment program, made by a multidisciplinary support team (primarily responsible clinician, dietician, psychologist and, if indicated, a speech therapist). At discharge and follow-up at 6, 12 and 18 weeks after discharge, food diaries (including growth) and questionnaires* relating to feeding behaviour and parental stress are filled out by parents/caregivers. One week before the planned outpatient visit of the patient and their parents, questionnaires will be sent with preferred software available in ErasmusMC ICT infrastructure through e-mail. The findings gathered from these nutritional data and questionnaires will be visualized on a dashboard (visible to parents and the caregivers) to discuss and help resolve the most relevant problems with the parents during the follow-up moments. During the outpatient visit, the growth and body composition of the child will also be assessed. The nutritional support team will discuss the outcomes of the questionnaires and make tailored advice based on the problems parents have reported. The dietician will discuss this tailored advice with the children and/or parents based on the growth, the nutritional intake of the child, and the problems parents have reported regarding the feeding behaviour of the child and their parental distress. Subsequently, the dietician will provide recommendations and psychoeducation to parents and/or patients in order to improve the nutritional status. At 6 months after discharge follow/up measurements such as, growth, duration and frequency of nutritional support, food diary, feeding behaviour of the child, QoL of the child, parental stress and QoL will be gathered. Evaluation and treatment other than follow-up at 6, 8 and 12 weeks after discharge with one of the health care professionals are on indication and data will not be collected. The intervention differs from the usual care, because follow-up is at standard time periods. In the usual care this is not regulated. Nutritional support is given in a multidisciplinary team including a psychologist, but in the pilot study we saw collaboration with the pediatrician and speech therapist only. In the intervention we also focuses on parenteral stress, which is new and different from usual care. Usual care group Nutritional advice in the usual care group will be given after discharge and follow-up according to standard practices. At 6 months after discharge an evaluation will be done equal to the intervention group. To collect information about the number of readmissions to the hospital and reason of admission, visits to a health-care provider, and growth parameters parents are asked to fill in a logbook to collect this data between discharge and 6 months follow-up. This method has been chosen because these are parameters that are difficult to remember at the visit 6 months after discharge. *The following age-adjusted and validated questionnaires will be used to assess emotional functioning, the pediatric feeding disorders, and parenteral stress:


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 260
Est. completion date March 31, 2027
Est. primary completion date March 31, 2026
Accepts healthy volunteers No
Gender All
Age group 7 Days to 18 Years
Eligibility Inclusion Criteria: - Children term born neonates till 18 years old - Admitted with newly initiated nutritional support(oral and/or enteral nutritional support) during hospitalization - Nutritional Support continues at home after discharge. Exclusion Criteria: - Children with existing nutritional support upon admission - Children in need of parenteral nutrition at discharge - Children with DSM-5 diagnosed feeding disorders such as anorexia - Absence of written informed consent

Study Design


Intervention

Other:
multidisciplinary structured tailored made nutritional advice
The goal is a structured follow-up after discharge. Parents need to fill in questionnaires about eating behavior en feeding difficulties about their child. They also need to fill in a questionnaire about their stress. Together with their nutritional intake (3-days food diary) and growth a tailor-made nutritional plan is made. All the information I showed in a dashboard and discussed it with their dietitian. Who discusses this information in a multi-disciplinary team (pediatrician, psychologist and if needed a speech therapist).

Locations

Country Name City State
Netherlands ErasmusMC Rotterdam Zuid-Holland

Sponsors (1)

Lead Sponsor Collaborator
Erasmus Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Weigth in kilograms and z-scores From enrollment until 6 months after discharge
Primary Height in meters and z-scores From enrollment until 6 months after discharge
Primary Head circumference in centimeters and z-scores From enrollment until 6 months after discharge
Primary Mid-upper arm circumference in centimeters and z-scores From enrollment until 6 months after discharge
Primary Length in children <2 years of age in centimeters and z-scores From enrollment until 6 months after discharge
Secondary Body composition Fat mass, Fat free mass From enrollment until 6 months after discharge
Secondary Duration and frequency of nutritional support Time (weeks), frequency per day From enrollment until 6 months after discharge
Secondary Dependency on nasogastric tube feeding Yes/No and intermitted or portions From enrollment until 6 months after discharge
Secondary Nutritional requirements and intake Energy as kcal/day and kcal/kg From enrollment until 6 months after discharge
Secondary Nutritional requirements and intake Protein as gram/day and gram/kg From enrollment until 6 months after discharge
Secondary Nutritional requirements and intake Fluids as ml/day and ml/kg From enrollment until 6 months after discharge
Secondary Nutritional requirements and intake Total mineral an vitamin intake percentage of ADH From enrollment until 6 months after discharge
Secondary Feeding behaviour of the child Questionnnaire CEBQ/BEBQ From enrollment until 6 months after discharge
Secondary Feeding behaviour of the child Questionnnaire MCH-FS From enrollment until 6 months after discharge
Secondary Parental stress Questionnaire LTO From enrollment until 6 months after discharge
Secondary Parental stress Questionnaire PROMIS From enrollment until 6 months after discharge
Secondary Quality of Life of children and parents Questionnaire CHU9D From enrollment until 6 months after discharge
Secondary Cost-effectiveness of tailored nutritional care Questionnaire iMCQ From enrollment until 6 months after discharge
Secondary Cost-effectiveness of tailored nutritional care Questionnaire iPCQ From enrollment until 6 months after discharge
Secondary Barriers and facilitators of implementation of the multidisciplinary support team Interviews with parents From enrollment until 6 months after discharge
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