CClinicalTrials.gg
CompletedNCT03836326Updated May 30, 2024

A Parent Administered Sensorimotor Intervention and Developmental Outcome of Preterm Infants

An interventional study of Sensorimotor intervention and Control in Premature Infant and Developmental Delay, sponsored by Dr. Sandra Fucile. Completed at 1 site in Canada. Open to participants aged Up to 34 Weeks. Per ClinicalTrials.gov, last updated 2024-05-30.

Sponsored by Dr. Sandra Fucile · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
94
Allocation
Randomized
Ages
Up to 34 Weeks
Sex
All
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Study summary

Advances in medical technologies over the last three decades have increased survival rates in infants born preterm . Preterm infants are at high risk of developing developmental delays. Implementation of effective strategies aimed at improving the developmental outcome of preterm born children is critical.

The proposed study is designed to evaluate the addition of a parent administered sensorimotor program on the developmental outcome of infants who are born preterm.

Read the detailed description

Children who are born prematurely are at a higher risk of developing developmental delays than children born at term. Early experiences in the neonatal intensive care unit (NICU) can influence developmental outcomes. Sensorimotor interventions as well as parental engagement have been designed with the aim of improving the development of children born preterm. Substantial evidence supports the benefits of each intervention on improving developmental outcomes. However, there remains a significant gap in the literature on the efficacy of a parent administered sensorimotor intervention (PASI) program in the NICU on infant's development. The proposed study is designed to evaluate the potential benefits of such a program on infant's development. A randomized block clinical trial will be performed.

A total of 84 preterm infants (\< 34 weeks gestation) will be recruited and randomized. Infants in the experimental group will receive the sensorimotor program,consisting of tactile (whole body) and oral input for 15 minutes, one time per day, for 10 days. Infants in the control group will receive standard care. The following outcomes will be monitored time to attainment of complete oral feeds (primary outcome), rate of weight gain, length of hospitalization, and developmental outcomes at 36 weeks corrected gestational age and at 4, 8, 12, 18 and 24 months corrected age. Results from this study will provide us with further knowledge on the impact of sensorimotor intervention on infants' developmental outcome as well as the effect of active parental involvement on infants' development. Provision of a PASI program is a safe and low cost effective intervention that may increase the development and quality of life of preterm born children and their family.

02

Conditions studied

  • Premature Infant
  • Developmental Delay

Keywords

  • Prematurity
  • Development
  • Parental engagement
  • Parental satisfaction
03

In context

Lead sponsor

Dr. Sandra Fucile is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 34 Weeks
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Infants born \< 34 weeks gestation
  • Infants whose parent (s) intend on visiting regularly (> 5 days)

Exclusion criteria

Exclusion Criteria:

  • Infants born with a metabolic disorder or congenital abnormality
  • Infants whose parents are unable to participate due to cognitive, physical or social issues.
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
94 participants (actual)

Study arms

  • Experimental
    Sensorimotor intervention

    Is a 15-minute intervention consisting of tactile (i.e., stroking the whole body) and oral input (i.e., stroking the oral structures) for 15 minutes duration. The program will start 24 hours after nasal continuous positive airway pressure (NCPAP) is discontinued and 24 hours after 80 ml/kg/day of enteral feeds are tolerated. The program will be administered once a day for 10 days, within a 14-day period. The parents will perform all the interventions in the NICU. The infants will remain in the isolette for the duration of the program. This intervention does not involve any drugs or medical procedures. It is an intervention commonly used by occupational and physical therapists in the neonatal intensive care unit.

    Other: Sensorimotor intervention · Other: Story telling attention refocusing intervention

  • Other
    Control

    Infants in the control group will receive standard care only.

    Other: Control

Interventions

  • OtherSensorimotor intervention

    Sensorimotor intervention involves, stroking of the whole body including the oral structures, trunk and limbs. This intervention does not involve any drugs or medical procedure.

    Also known as: Supplemental stimulation, Sensory input, Tactile input, Oral input

  • OtherControl

    Routine care provided by health professionals in the NICU

  • OtherStory telling attention refocusing intervention

    A contact-free intervention where parents share stories with their infant for 10 minutes 3 times per week.

    Also known as: STAR

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What researchers measure

Primary outcomes

  1. Attainment of independent oral feeds

    Number of days to transition from complete tube to complete oral feeds.

    Time frame: 3 years

Secondary outcomes

  1. Weight gain

    Weight gain velocity from start of study until hospital discharge

    Time frame: 3 years

  2. Length of hospital stay

    Number of days from birth to discharge home

    Time frame: 3 years

  3. Test of infant motor performance

    A standardized assessment measuring postural control and motor function in infants from 32 weeks gestation to 4 months corrected gestational age. Total raw scores range from 0-142, higher scores represent better motor function.

    Time frame: 3 years

  4. Acute stress of parents

    The PSS: NICU assessment was used to assess acute stress of parents

    Time frame: 3 years

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Study locations

1 site
  • Kingston Health Sciences Center
    Kingston, Ontario k7l2v7, Canada
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 30, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03836326
Lead sponsor
Dr. Sandra Fucile
Responsible party
Dr. Sandra Fucile (PI, Kingston Health Sciences Centre) — Sponsor-investigator
First posted
Feb 11, 2019
Start date
Jul 1, 2019
Primary completion
May 1, 2024
Completion
May 1, 2024
Last update
May 30, 2024

Study contacts

Sandra Fucile, PhD
principal investigator · Kingston Health Sciences Centre

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2024. You cannot join it, but the record below documents what was studied.

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