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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04666857
Other study ID # EMI
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 31, 2021
Est. completion date February 20, 2023

Study information

Verified date September 2023
Source University Children's Hospital, Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study the investigators aim to test the feasibility for therapists and acceptability to parents of an early motor intervention for infants with congenital heart disease (CHD) after open heart surgery. This intervention will be compared to the standard care of treatment that is recommended for infants with congenital heart disease at the University Children Hospital Zurich.


Description:

In this feasibility pilot randomised study children will be randomly assigned to a control and an intervention group. Children of the control group will receive standard of care for infants with severe CHD: cardiac surveillance, counselling and screening at the University Children's Hospital Zurich and standardised developmental checkups by their paediatrician. Physiotherapy is normally not comprised in standard of care, but some infants may receive physiotherapy, if they present with obvious signs of motor developmental delay, detected by the paediatrician later on in their life. Once enrolled in this study, an infant of the control group will not receive early motor intervention as an infant enrolled in the intervention group. Infants randomly assigned to the intervention group will receive early motor intervention, which will be based on the results of our qualitative study. It will comprise supporting parents by a paediatric physiotherapist. Parents will be guided on how to best stimulate their infant's development during daily activities. Parents will be actively involved in the intervention with the aim to challenge their infant at the limit of its postural capacity and thus help the infant to optimize its motor repertoire. The intervention will start after baseline with infants aged 3-6 months and end after three months with infants aged 6-9 months. The intervention will start at home, then alternating at the Children's Hospital and at home. Telephone or video counselling will be provided to support parents if needed. The order may change according to the needs of the family when necessary and adjusted to best fit the daily routine the family.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date February 20, 2023
Est. primary completion date December 19, 2022
Accepts healthy volunteers No
Gender All
Age group 2 Months to 12 Months
Eligibility Inclusion Criteria: - Infants born with severe cyanotic and acyanotic congenital heart disease (e.g. tetralogy of Fallot, pulmonary atresia, transposition of the great arteries, atrial/ventricular septal defects, double outlet right ventricle, ...) who undergo open-heart surgery once before the first 3-6 months of their life - Parents able to comprehend the patient information linguistically and cognitively - Informed consent of parents as documented by signature Exclusion Criteria: - Infants with hypoplastic left heart syndrome as they need to undergo several open-heart surgeries within the first period of their life. - Infants with trisomy 21 and other syndromes like 22q11 microdeletion syndrome, CHARGE syndrome that are often associated with CHD. These infants often show additional cognitive impairments that might confound the effect of our intervention.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
early motor intervention
infants with CHD after open heart surgery will receive early intervention

Locations

Country Name City State
Switzerland University Children's Hospital Zürich

Sponsors (1)

Lead Sponsor Collaborator
University Children's Hospital, Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Other Hammersmith Infant Neurological Examination The Hammersmith Infant Neurological Examination assesses different aspects of neurological function.
the higher the scores the better, the range depends on the child's abilities metric: ordinal
"3 up to 6 months of age" (baseline) and at "12 months of age"
Other General Movements The General Movement assessment is a video-based, non-invasive way to identify neurological deviations that may lead to neurodevelopmental disorders later in life.
The more variables the motor output of infants, the better infants' neuromotor development will be.
metric: categorial
"3 up to 6 months of age" (baseline)
Other Infant Motor Profile The Infant Motor Profile is a standardised and qualitative method to assess motor behaviour in infants, a 15 minutes, video-based assessment tool, consists of 5 domains: motor variation, adaptability, symmetry, fluency and performance.
The higher the score, the better - the range depends on the child's abilities and is age dependent metric: ordinal
"3 up to 6 months of age" (baseline), "6 up to 9 months of age" (end of intervention), at "12 months of age"
Other Alberta Infant Motor Scale Change in being assessed at different time points at baseline, at the end of the intervention after three months and at follow up The Alberta Infant Motor Scale is an observational measure of infants' gross motor development from birth until 18 months consisting of 58 items, measuring infants' performance; The higher the score, the better, the range depends on the child's abilities and is age dependent
metric: ordinal
"3 up to 6 months of age" (baseline), "6 up to 9 months of age" (end of intervention) and at "12 months of age"
Other Bayley Scale for Infant and Toddlers Development Bayley Scale for Infant and Toddlers Development is an internationally used and validated battery to assesses key domains of cognition, language, socio-emotional, motor and adaptive behaviour by standardized observation and rating of the play behaviour of children the higher the scores the better, the range depends on the child's abilities and is age dependent metric: ordinal "around 12 months of age"
Other Parental Stress Index The Parental Stress Index investigates parental stress of children with all different kind of diagnoses, consists of 5 subscales assessing areas where parental strain is high; the Parental Stress Index consists of 48 items the lower, the score the better
metric: ordinal
"3 up to 6 months of age" (baseline), "6 up to 9 months of age" (end of intervention) and at "12 months of age"
Other Brief Symptom Inventory 18 The Brief Symptom Inventory 18 contains a three six-item scales somatization, depression, and anxiety as well as the Global Severity Index the lower, the score the better
metric: ordinal
"3 up to 6 months of age" (baseline), "6 up to 9 months of age" (end of intervention) and at "12 months of age"
Other Parental Overprotection Measure The Parental Overprotection Measure assesses parenting behaviours that restrict a child's exposure to situations containing perceived threat or harm.
the higher the scores the more parents protect their children metric: ordinal
"3 up to 6 months of age" (baseline), "6 up to 9 months of age" (end of intervention) and at "12 months of age"
Other Family Empowerment Scale The Family Empowerment Scale measures empowerment of families. It consists of three subscales, family, service system and community/political. We use the subscale family to gather relevant information as a result of an intervention.
the higher the scores the more the family feels empowered metric: ordinal
"3 up to 6 months of age" (baseline), "6 up to 9 months of age" (end of intervention) and at "12 months of age"
Other Quality of life form Short Form 36 The Quality of life form Short Form 36 is a widely used questionnaire assessing self-reported health related quality of life the lower the score the better
metric: ordinal
"3 up to 6 months of age" (baseline), "6 up to 9 months of age" (end of intervention) and at "12 months of age"
Other Pediatric Quality of Life Inventory The Pediatric Quality of Life Inventory measures quality of life of infants aged 1- 24 months.
the higher the scores the more the quality of life is affected. metric: ordinal
"3 up to 6 months of age" (baseline), "6 up to 9 months of age" (end of intervention) and at "12 months of age"
Primary Dropout rate The primary outcome will test the procedure for its acceptability, estimation the likely rates of recruitment and retention of subjects and the calculation of appropriate sample size. Further objectives are the usefulness of the outcome assessment measures. "3 up to 6 months of age" (baseline) and at "12 months of age"
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