Visual Stimulation of Preterm Infants

Preterm Infant Clinical Trial

Official title:

Early Visual Stimulation in Preterm Infants at Home From 0 to 3 Months

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03302000
• Other study ID #: UFSC-SIGPEX / 201610782
• Status: Completed
• Phase: N/A
• Start date: September 1, 2018
• Est. completion date: December 31, 2019

Study information

• Verified date: June 2020
• Source: Universidade Federal de Santa Catarina
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Introduction: Prematurity rate has increased and is a risk factor for developmental delay. Preterm infants with low visual tracking might present deficits in cognition, language, and fine motor function in future ages. Few studies applied home stimulation of the visual system for preterm infant (PT) at an early age.

Objective: To compare the effects of early visual stimulation to a standard care group in visual function, motor and sensory development.

Methods: Randomized controlled trial. At home setting. Thirty healthy preterm infants, gestational age from 28 to 37 weeks, aged from one to two months of corrected age at the entrance of the study, with low visual function, will be evaluated. Participants will be randomly allocated to: (1) a standard care group, receiving orientation about general sensory and motor development, (2) an early visual stimulation group receiving a 4-week home based protocol applied by caregivers additional to standard care. Outcomes will be measured at before the beginning of stimulation, at the end of stimulation and at 6 months of corrected age. Primary outcome is visual function evaluated by ML Leonhardt Battery of Optotypes. Secondary outcomes include motor and sensory development evaluated by scales.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: December 31, 2019
• Est. primary completion date: December 30, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 1 Month to 2 Months

Eligibility

Inclusion Criteria:

• gestational age between 28 and 37 weeks

• age at enrolment between one to two months of corrected age t

• absence of visual impairments evaluated with Red Reflex Examination and complete ophthalmology exam, which will be performed by a doctor at the hospital or the basic health units where the infants will be recruited

• infants at home

• presence of low acuity assessed by the ML-Leonhardt Optotypes Battery (absence of alertness, fixation and attention in at least three cards, or visual tracking classified as absent or brief for more than three cards)

Exclusion Criteria:

• presence of any diagnosed neurological diseases

• presence of diagnosed respiratory diseases

• hypoxemia, hyperventilation or hypo-ventilation during assessments

• presence of congenital diseases

• presence of diagnosed visual impairments, such as blindness or low vision

• extreme premature, ie, with gestation age bellow 28 weeks due to higher risk of retinopathy of prematurity

• birth weight less than 1,000 grams due to higher risk of retinopathy of prematurity

• absence of alertness according with Precthl and Beintema

• preterm infant with unstable physiological conditions

• preterm infant receiving any kind of intervention such as physical therapy, occupational therapy, early intervention, aquatic stimulation, at the same time that our stimulation protocol is being applied since they can be confounders

• infants with medical fragility that prevent them to participate.

Related Conditions & MeSH terms

• Premature Birth
• Preterm Infant

Intervention

Other:
• Early Visual Stimulation
Early visual stimulation
• standard care
standard care

Locations

Country	Name	City	State
Brazil	Universidade Federal de Santa Catarina	Araranguá	Santa Catarina

Sponsors (1)

Lead Sponsor	Collaborator
Universidade Federal de Santa Catarina

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Visual function - alertness, fixation, attention, tracking	Visual acuity will be assessed with ML Leonhardt Battery of Optotypes (MLLBOS) scale. MLLBOS consists of 8 visual carts, with high-contrast visual images of 12X12cm. The scale evaluates alertness, attention, fixation and visual tracking. The evaluation will be recorded by a digital video camera. The camera will be positioned fixed to the infant's face.	change measure: first day - before intervention; after intervention at home (28 days)
Secondary	Sensory profile	Infant Sensory Profile Scale (SPS) is a 125 item, norm-referenced, parent-report questionnaire. Sensory processing is divided in six items: general processing, auditory processing, visual processing, tactile processing, vestibular processing and oral sensory processing.	change measure: first day - before intervention; after intervention at home (28 days); at 6 months of corrected age
Secondary	Motor Development	Motor development will be assessed with Test of Infant Motor Performance (TIMP). It is a functional motor scale for newborn infants and infants under 4 months of age. Twenty-eight Observed Items examine spontaneously emitted movements, such individual finger, ankle and wrist movements. Thirty-one Elicited Items, scored on 5-, 6-, or 7-point ordinal scales, test infant's movement responses to placement in various spatial orientations and to interesting sights and sounds.	change measure: first day - before intervention; after intervention at home (28 days)
Secondary	Motor Development	Motor development will be assessed with Alberta Infant Motor Scale (AIMS). The AIMS is a validated and reliable measure of infant's development. The assessors observe the spontaneous repertoire of infant's skills detected through 58 items grouped under four postures: prone (21 items), supine (9 items), sitting (12 items), and standing (16 items)	change measure: at 6 months of corrected age